Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and...

68
Biopharmaceutical Filtration Solutions Making the Filtration Better

Transcript of Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and...

Page 1: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

Biopharmaceutical

Filtration Solutions

Hangzhou Anow Microfiltraion Co.,Ltd.Office:Room 901-903, Central Building, No.271, Hushu South Road, Hangzhou, China

Plant: Qingming Bridge, Xindeng Industrial Zone, Fuyang, Hangzhou, China

Tel: +86-571-883-70389

Fax: +86-571-883-70399

Website: www.anowfilter.com

E-mail: [email protected]

Making the Filtration Better

Page 2: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Located in Hangzhou, 's plant covers a

2production workshop area of 6000 m , with 3000

2m area meeting the GMP requirements for

2 5manufacturing of medical devices, 600 m 10 -

2class cleaning room and 2400 m cleaning room.

We have more than twenty lines for the

production of microporous membranes and

pleated filter cartridges, advanced inspection

tools and equipments, as well as professional

R&D Center and Validation Center. All the

membrane products are manufactured in

ISO9001:2008 certified facility with the help of

trained manpower meeting or exceeding

industry standards.

ANOW

www.anowfilter.com

COMPANY INTRODUCTION

ANOW

ANOW

Microfiltration is a well-known filtration leader,started from 1989, who focus on research and

development of MCE, Nylon, PES, PVDF, PTFE membrane, with pore size ranging from 0.03 μm to 10

μm, as well as design and production of various pleated filter cartridges, syringe filters and capsule

filters. provides professional assistances to liquid and gas & air filtration solutions for

customers around the world in biopharmaceutical, medical, food & beverage, microelectronic,

chemistry, water treatment and laboratory applications.

In biopharmaceutical industry, products

are used in highly regulated industries for critical

applications such as sterile filtration of

pharmaceutical and biopharmaceutical

process fluids, sterility testing of aseptic drug

products, analytical sample preparation, new

drug development and so on.

ANOW

has been making great efforts to improve

the quality management system during the

process of obtaining the production certificates

and registration. We help to deliver an ever

increasing portfolio of innovative products with

unique performance advantages.

ANOW

www.anowfilter.com

CONTENTS

2 1

COMPANY INTRODUCTION

CONTENTS

ANOW Membrane Technologies

Quality Assurance

Validation Service

Customer Support

Facilities Water

Cell Culture Media Preparation

Small Volume Parenterals (SVP)

Large Volume Parenterals (LVP)

Plasma Fractionation

Ophthalmic Solutions

Filter Cartridges

LPSL-Low Extractable and Longer Service Life Filter Cartridge with Double Layer PES Membrane

13

15

17

19

21

23

27

29

25

55

57

61

63

Filter Housings

59

Connections 66

1

2

3

4

LPSHT-Highly Asymmetric PES Filter

Cartridge for Higher Throughput Demands

LPSHV-PES Filter Cartridge for Sterile

Filtration of High Viscous Pharmacy

LPS-Single Layer Hydrophilic PES Filter

Cartridge for Final Filtration of Pharmacy

LPSD-Double Layer Hydrophilic PES

Filter Cartridge for Extremely

Demanding of Sterilizing Filtration

LPT-Hydrophobic PTFE Filter

Cartridge with Broad Chemical Compatibility

LPTA-Hydrophobic PTFE Filter

Cartridge for Sterilizing Filtration of Air/Gas

LPNN-Hydrophilic Nylon Filter

Cartridge for Sterile Filtration of

Facilities Water & API

LPTL-Hydrophilic PTFE Filter

Cartridge for Solvent Filtration

LPGF-Glass Fiber Filter Cartridge

for Prefiltration of Viscous

Pharmacy and Vaccines

Hydrophilic Nylon Membrane

Hydrophilic PES Membrane

Hydrophilic MCE Membrane

Hydrophobic PTFE Membrane

Hydrophobic PVDF Membrane

HY Stainless Steel Filter Housing for Sanitary Liquid Filtration

Series

HK Stainless Steel Filter

Housing for Gas&Air Filtration

Series

HM Sanitary Disc HolderSeries Filter

HT Titanium Filter HousingSeries

HG Sanitary In-line Liquid

and Gas Filter Housing

Series

Chemical Compatibility Guide

5

6

7

8

9

10

11

12

31

33

35

37

39

LPM-Hydrophilic MCE Filter

Cartridge for Prefiltration of Biologicals

LPV-Hydrophobic PVDF Filter

Cartridge with Low Protein Binding

LPP-The Most Economical PP

Filter Cartridge for Prefiltration

LPPF-The Most Efficient multi-layer

PP Filter Cartridge for Prefiltration

LPAP-Absolute PP Filter Cartridge

for Active Pharmaceutical Ingredients

41

53

53

53

53

53

65

Applications

Membranes

CTP Tri-Clamp Capsule Filter for

Small Volume & High

Value-added Pharmacy

CHP Hose Barb Capsule Filter

for Small Volume & High

Value-added Pharmacy

CNP 1/4" NPT Capsule Filter for Small Volume & High Value-added Pharmacy

F5P φ50 Filter Unit

®Easiprep φ5/ Syringe Filter

φ13/φ20/φ25/φ33

43

45

47

49

51

Capsule Filters & Syring Filters

Page 3: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Located in Hangzhou, 's plant covers a

2production workshop area of 6000 m , with 3000

2m area meeting the GMP requirements for

2 5manufacturing of medical devices, 600 m 10 -

2class cleaning room and 2400 m cleaning room.

We have more than twenty lines for the

production of microporous membranes and

pleated filter cartridges, advanced inspection

tools and equipments, as well as professional

R&D Center and Validation Center. All the

membrane products are manufactured in

ISO9001:2008 certified facility with the help of

trained manpower meeting or exceeding

industry standards.

ANOW

www.anowfilter.com

COMPANY INTRODUCTION

ANOW

ANOW

Microfiltration is a well-known filtration leader,started from 1989, who focus on research and

development of MCE, Nylon, PES, PVDF, PTFE membrane, with pore size ranging from 0.03 μm to 10

μm, as well as design and production of various pleated filter cartridges, syringe filters and capsule

filters. provides professional assistances to liquid and gas & air filtration solutions for

customers around the world in biopharmaceutical, medical, food & beverage, microelectronic,

chemistry, water treatment and laboratory applications.

In biopharmaceutical industry, products

are used in highly regulated industries for critical

applications such as sterile filtration of

pharmaceutical and biopharmaceutical

process fluids, sterility testing of aseptic drug

products, analytical sample preparation, new

drug development and so on.

ANOW

has been making great efforts to improve

the quality management system during the

process of obtaining the production certificates

and registration. We help to deliver an ever

increasing portfolio of innovative products with

unique performance advantages.

ANOW

www.anowfilter.com

CONTENTS

2 1

COMPANY INTRODUCTION

CONTENTS

ANOW Membrane Technologies

Quality Assurance

Validation Service

Customer Support

Facilities Water

Cell Culture Media Preparation

Small Volume Parenterals (SVP)

Large Volume Parenterals (LVP)

Plasma Fractionation

Ophthalmic Solutions

Filter Cartridges

LPSL-Low Extractable and Longer Service Life Filter Cartridge with Double Layer PES Membrane

13

15

17

19

21

23

27

29

25

55

57

61

63

Filter Housings

59

Connections 66

1

2

3

4

LPSHT-Highly Asymmetric PES Filter

Cartridge for Higher Throughput Demands

LPSHV-PES Filter Cartridge for Sterile

Filtration of High Viscous Pharmacy

LPS-Single Layer Hydrophilic PES Filter

Cartridge for Final Filtration of Pharmacy

LPSD-Double Layer Hydrophilic PES

Filter Cartridge for Extremely

Demanding of Sterilizing Filtration

LPT-Hydrophobic PTFE Filter

Cartridge with Broad Chemical Compatibility

LPTA-Hydrophobic PTFE Filter

Cartridge for Sterilizing Filtration of Air/Gas

LPNN-Hydrophilic Nylon Filter

Cartridge for Sterile Filtration of

Facilities Water & API

LPTL-Hydrophilic PTFE Filter

Cartridge for Solvent Filtration

LPGF-Glass Fiber Filter Cartridge

for Prefiltration of Viscous

Pharmacy and Vaccines

Hydrophilic Nylon Membrane

Hydrophilic PES Membrane

Hydrophilic MCE Membrane

Hydrophobic PTFE Membrane

Hydrophobic PVDF Membrane

HY Stainless Steel Filter Housing for Sanitary Liquid Filtration

Series

HK Stainless Steel Filter

Housing for Gas&Air Filtration

Series

HM Sanitary Disc HolderSeries Filter

HT Titanium Filter HousingSeries

HG Sanitary In-line Liquid

and Gas Filter Housing

Series

Chemical Compatibility Guide

5

6

7

8

9

10

11

12

31

33

35

37

39

LPM-Hydrophilic MCE Filter

Cartridge for Prefiltration of Biologicals

LPV-Hydrophobic PVDF Filter

Cartridge with Low Protein Binding

LPP-The Most Economical PP

Filter Cartridge for Prefiltration

LPPF-The Most Efficient multi-layer

PP Filter Cartridge for Prefiltration

LPAP-Absolute PP Filter Cartridge

for Active Pharmaceutical Ingredients

41

53

53

53

53

53

65

Applications

Membranes

CTP Tri-Clamp Capsule Filter for

Small Volume & High

Value-added Pharmacy

CHP Hose Barb Capsule Filter

for Small Volume & High

Value-added Pharmacy

CNP 1/4" NPT Capsule Filter for Small Volume & High Value-added Pharmacy

F5P φ50 Filter Unit

®Easiprep φ5/ Syringe Filter

φ13/φ20/φ25/φ33

43

45

47

49

51

Capsule Filters & Syring Filters

Page 4: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com www.anowfilter.com

ANOW Membrane Technologies

membrane products are well designed with built-in quality assurance. We introduce the most stringent Quality

Management System covering careful selection of raw material, validated manufacturing process, quality control

and assurance and so on. All this is to ensure consistently offer high quality products for our customers.

ANOW

brings more than 26 years of

experience in membrane technology to the

biopharmaceutical, medical, laboratory, food

& beverage, microelectronic and chemical

applications. And we have been continuously

working to provide customized filtration solutions

with high quality.

ANOW

Quality Assurance

3 4

ISO Certified

Complete Traceability

Certificate of Products

Deep Characterization and Certification

ANOW

Page 5: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com www.anowfilter.com

ANOW Membrane Technologies

membrane products are well designed with built-in quality assurance. We introduce the most stringent Quality

Management System covering careful selection of raw material, validated manufacturing process, quality control

and assurance and so on. All this is to ensure consistently offer high quality products for our customers.

ANOW

brings more than 26 years of

experience in membrane technology to the

biopharmaceutical, medical, laboratory, food

& beverage, microelectronic and chemical

applications. And we have been continuously

working to provide customized filtration solutions

with high quality.

ANOW

Quality Assurance

3 4

ISO Certified

Complete Traceability

Certificate of Products

Deep Characterization and Certification

ANOW

Page 6: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com www.anowfilter.com

Integrity Test

Confirm the correlation of integrity test values which

were gotten under both standard and process fluid

conditions.

Bacterial Challenge Test

According to ASTM F838 methodology, testify bacterial

retention capability of membrane or filter at a minimum

7 2concentration of 10 cfu/cm of filter surface area,

under simulated process conditions.

Chemical Compatibility

Ensure the compatibility of filter and process fluid.

Ensure the reliability of filter in process condition.

Provide supportive data for filter selection.

Extractables

Determine all the chemical components that migrate

from membranes or filters into a drug product or process

fluid in proper solvents in worst case. It indicates

maximum possibility of chemical components migrating

from membranes or filters.

Adsorption

Measure the adsorption ability of filter media in fluid

filtration process.

Multi-use Validation

Confirm retention capacity of cartridges in normal

process or simulated conditions after multiple uses.

Filter Cleaning

Provide the filter cleaning method for the specific fluid

filtration.

Sterilizing filtration for pharmaceutical liquids is indispensable and critically important in aseptic manufacturing. It is the

process of removing bioburden, particles and bacterial endotoxins from a fluid stream without adversely affecting drug

product quality. With years of experiences in pharmaceutical research, more details and supportive data were found

that the sterilizing filtration is a high risk process, whose risk is next only to that of sterilizing making and filling. Only if it gets

through with validation, we could be sure of the compatibility, extractables/leacheables and adsorption, then to confirm the

reliability of sterilizing filtration. Besides, GMP, FDA and PDA described the requirements for sterilizing filtration validation

under specific conditions.

can offer validation services, designed to the unique needs of each customer's fluid and set of process conditions,

and help to prepare normative documents to achieve regulatory compliance. These include the following items:

ANOW

Validation Service

has always been working to support your

applications and welcomes the opportunity to assist

you in the education of your staff.

ANOW

Customer Support

Customized Filtration Solutions

We offer customized solutions for complex

filtration problems. And we will help you in finding

suitable solutions with minimizing filtration cost.

Filtration System Design

offers technical support for your selection of

filter materials, cartridge length, filter housing and

performing throughput studies to optimize filter sizing

with cost-effective filtration system.

ANOW

Installation and Operation Training

filtration specialists are available to assist

customers with theory training and hands-on

installation and operation training.

ANOW

Technical Seminars

Technical seminars at customer’s location are

organized to help the users better understand

standard operation procedures of products, thus

to improve the performance and to extend the

service life of products. Besides, technical exchanges

can also be helpful for users to select the optimized

solutions for their applications.

5 6

ANOW offers an extensive range of support including

validation, filtration education, installation training,

and other experience sharing that customers need.

Page 7: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com www.anowfilter.com

Integrity Test

Confirm the correlation of integrity test values which

were gotten under both standard and process fluid

conditions.

Bacterial Challenge Test

According to ASTM F838 methodology, testify bacterial

retention capability of membrane or filter at a minimum

7 2concentration of 10 cfu/cm of filter surface area,

under simulated process conditions.

Chemical Compatibility

Ensure the compatibility of filter and process fluid.

Ensure the reliability of filter in process condition.

Provide supportive data for filter selection.

Extractables

Determine all the chemical components that migrate

from membranes or filters into a drug product or process

fluid in proper solvents in worst case. It indicates

maximum possibility of chemical components migrating

from membranes or filters.

Adsorption

Measure the adsorption ability of filter media in fluid

filtration process.

Multi-use Validation

Confirm retention capacity of cartridges in normal

process or simulated conditions after multiple uses.

Filter Cleaning

Provide the filter cleaning method for the specific fluid

filtration.

Sterilizing filtration for pharmaceutical liquids is indispensable and critically important in aseptic manufacturing. It is the

process of removing bioburden, particles and bacterial endotoxins from a fluid stream without adversely affecting drug

product quality. With years of experiences in pharmaceutical research, more details and supportive data were found

that the sterilizing filtration is a high risk process, whose risk is next only to that of sterilizing making and filling. Only if it gets

through with validation, we could be sure of the compatibility, extractables/leacheables and adsorption, then to confirm the

reliability of sterilizing filtration. Besides, GMP, FDA and PDA described the requirements for sterilizing filtration validation

under specific conditions.

can offer validation services, designed to the unique needs of each customer's fluid and set of process conditions,

and help to prepare normative documents to achieve regulatory compliance. These include the following items:

ANOW

Validation Service

has always been working to support your

applications and welcomes the opportunity to assist

you in the education of your staff.

ANOW

Customer Support

Customized Filtration Solutions

We offer customized solutions for complex

filtration problems. And we will help you in finding

suitable solutions with minimizing filtration cost.

Filtration System Design

offers technical support for your selection of

filter materials, cartridge length, filter housing and

performing throughput studies to optimize filter sizing

with cost-effective filtration system.

ANOW

Installation and Operation Training

filtration specialists are available to assist

customers with theory training and hands-on

installation and operation training.

ANOW

Technical Seminars

Technical seminars at customer’s location are

organized to help the users better understand

standard operation procedures of products, thus

to improve the performance and to extend the

service life of products. Besides, technical exchanges

can also be helpful for users to select the optimized

solutions for their applications.

5 6

ANOW offers an extensive range of support including

validation, filtration education, installation training,

and other experience sharing that customers need.

Page 8: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Cells used to produce therapeutic proteins should have a precise nutritional balance to support their reproduction

and growth. These nutrients are provided by culture media, which must be sterile. Final sterilizing filtration should assure

the removal of bacteria and mycoplasma from culture media containing animal derived components.

Culture media are then stored in a fermentation vessel or bioreactor after bulk preparation and sterilizing filtration.

Prefilters are used to remove most particulate and colloidal contaminants from culture media in order to extend the

service life of final sterilizing filters.

Separation Goals

www.anowfilter.com7

Cell Culture Media Preparation

● Prefiltration

Remove colloids, lipids and particles

● Sterilizing filtration

Remove bacteria and mycoplasma

Application Requirements

● Prefiltration should remove particulate and colloidal contaminants effectively and not hinder the bypass of important

components.

● Prefilters must have high flow rates and consistent high throughputs in order to finish the separating process timely and

economically. Furthermore, the filtration system should be compatible with differences, resulting from batch to batch

component variability.

Recommendation

Filtration Step Recommendation

Prefiltration LPM, LPGF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSL

Prefiltration Sterile Filtration Sterile Holding Tank Final Filtration Bioreactor Fermentor

SterileVenting SterileVenting

Mix Tank

Media Powder

WFI

www.anowfilter.com 8

Facilities Water

Pharmaceutical grade water is defined as feed water common to process systems such as washers, autoclaves

or WFI systems. Since water source varies widely in quality, only appropriate filtration systems can ensure the

production to be effective, safe and successful.

Filtration is just one step of the manufacturing process of pharmaceutical grade water. Other steps may result in

the increasing of particles, for both resin and activated carbon beds could produce powder.

Separation Goals

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of final filters.

● Final Filtration

Remove particles, microorganisms and endotoxins to meet the requirements of FDA and other international standards.

Application Requirements

● Prefilters must remove most particulate and colloidal contaminants effectively, and have high dirt-holding

capacity, and keep high flow rates and high throughputs.

● Final filters must remove microorganisms and endotoxins, and keep high flow rates and high throughputs.

Filtration Step Recommendation

Prefiltration LPP, LPM, LPGF

Sterile venting LPTA

Final filtration LPS

LPNN for removing endotoxins

Filters with positive charge have limited capacity of removing endotoxins. Once the capacity is saturated, they lose this

ability of removing endotoxins. Series connection of two filters is the solution, monitoring the endotoxins between the two

filters. When endotoxins exist in the downstream of the first filter, the second filter should replace the first one in its position.

This can make full use of filters and ensure reliable retention rate. Replacement of filters with no charge depends on pre-

setting limitation index such as maximum differential pressure, minimum flow rate and maximum life time.

Recommendation

Prefiltration Sterile Filtration Final FiltrationCompression

Air

Point of Use

Prefiltration Sterile Filtration Sterile Holding Tank Final Filtration

SterileVenting

Water

Endotoxin

Removal

Point of Use

Page 9: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Cells used to produce therapeutic proteins should have a precise nutritional balance to support their reproduction

and growth. These nutrients are provided by culture media, which must be sterile. Final sterilizing filtration should assure

the removal of bacteria and mycoplasma from culture media containing animal derived components.

Culture media are then stored in a fermentation vessel or bioreactor after bulk preparation and sterilizing filtration.

Prefilters are used to remove most particulate and colloidal contaminants from culture media in order to extend the

service life of final sterilizing filters.

Separation Goals

www.anowfilter.com7

Cell Culture Media Preparation

● Prefiltration

Remove colloids, lipids and particles

● Sterilizing filtration

Remove bacteria and mycoplasma

Application Requirements

● Prefiltration should remove particulate and colloidal contaminants effectively and not hinder the bypass of important

components.

● Prefilters must have high flow rates and consistent high throughputs in order to finish the separating process timely and

economically. Furthermore, the filtration system should be compatible with differences, resulting from batch to batch

component variability.

Recommendation

Filtration Step Recommendation

Prefiltration LPM, LPGF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSL

Prefiltration Sterile Filtration Sterile Holding Tank Final Filtration Bioreactor Fermentor

SterileVenting SterileVenting

Mix Tank

Media Powder

WFI

www.anowfilter.com 8

Facilities Water

Pharmaceutical grade water is defined as feed water common to process systems such as washers, autoclaves

or WFI systems. Since water source varies widely in quality, only appropriate filtration systems can ensure the

production to be effective, safe and successful.

Filtration is just one step of the manufacturing process of pharmaceutical grade water. Other steps may result in

the increasing of particles, for both resin and activated carbon beds could produce powder.

Separation Goals

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of final filters.

● Final Filtration

Remove particles, microorganisms and endotoxins to meet the requirements of FDA and other international standards.

Application Requirements

● Prefilters must remove most particulate and colloidal contaminants effectively, and have high dirt-holding

capacity, and keep high flow rates and high throughputs.

● Final filters must remove microorganisms and endotoxins, and keep high flow rates and high throughputs.

Filtration Step Recommendation

Prefiltration LPP, LPM, LPGF

Sterile venting LPTA

Final filtration LPS

LPNN for removing endotoxins

Filters with positive charge have limited capacity of removing endotoxins. Once the capacity is saturated, they lose this

ability of removing endotoxins. Series connection of two filters is the solution, monitoring the endotoxins between the two

filters. When endotoxins exist in the downstream of the first filter, the second filter should replace the first one in its position.

This can make full use of filters and ensure reliable retention rate. Replacement of filters with no charge depends on pre-

setting limitation index such as maximum differential pressure, minimum flow rate and maximum life time.

Recommendation

Prefiltration Sterile Filtration Final FiltrationCompression

Air

Point of Use

Prefiltration Sterile Filtration Sterile Holding Tank Final Filtration

SterileVenting

Water

Endotoxin

Removal

Point of Use

Page 10: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Large Volume Parenterals (LVPs) are single unit doses more than 50 cc. Prefiltration is used for removing particles to

extend the service life of final (sterilizing) filtration. Final filters are used for reducing bioburden or sterile filtration prior

to terminal sterilization. The volume of LVPs is usually tens of thousands of liters, and multiple filling lines may be working

at the same time.

Ingredients in typical LVP solutions include water, dextrose (from 5% to 50%), amino acid, salts and very viscous total

parenteral nutrition (TPN). Prefilters are used to reduce particles for salt solutions, and to remove hard particles for

dextrose solutions before final sterilizing filtration (it's another option to reduce bioburden by using 0.45 μm filters)

www.anowfilter.com9

Large Volume Parenterals (LVP)

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of downstream sterilizing filters

● Final filtration

Reduce bioburden prior to terminal sterilization (0.45 μm)

Sterile filtration prior to terminal sterilization (0.22 μm)

● LVP filters must provide consistent high flow rates to ensure the accuracy and consistency of filling.

● Since typical LVP filling process is operated under high differential pressure and high flow rates, filters must have superior

mechanical strength and be reliable and robust.

● The cost of LVP filters must be economical.

● Prefilters and sterilizing filters must bear multiple cycles of steam-in-place sterilization or hot water sanitization.

Filtration Step Recommendation

Prefiltration LPP, LPPF

Sterile venting LPTA

Final filtration LPS

Separation Goals

Application Requirements

Recommendation

PrefiltrationSterile

Holding

Tank

Final

Filtration

SterileVenting

Mix Tank

Powder

WFI

Filling Autoclave PackagingBioburden

Reduction

www.anowfilter.com 10

Small Volume Parenterals (SVP)

Small volume parenterals (SVP) include various traditional and bioengineered drugs. These drugs are usually packaged in

small vials (less than 20 ml), pre-filled syringes and ampoules, or made in lyophilized powder. Lots of SVPs need aseptic

processing for their lack of heat-stability.

Sterilizing filtration is used after synthesis or before filling. And it can add the sterility assurance if sterilizing filtration is used

at both locations. Prefilters should be used to reduce bioburden and particles, which would clog final filters prematurely.

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of downstream sterilizing filters

● Final filtration

Provide a sterile filtrate meeting the requirements of current regulatory

Separation Goals

● Final sterilizing filters should remove bacteria without altering the effects of drug products. Therefore, these filters

should have low adsorption of active pharmaceutical ingredient (API), low extractables, be non-pyrogenic and

integrity testable, and be sterile or can be sterilized.

● Prefilters and final filters should have enough flow rates. Final filters in the filling machine must have strong structures

to prevent media flexing during pulsed flow filling processing, which will result in particle release, drips or other

dispense problems.

Filtration Step Recommendation

Prefiltration LPP, LPM

Sterile venting LPTA

Final filtration LPS, LPSD

Application Requirements

Recommendation

PrefiltrationMix Tank

SterileVenting

Active

Pharmacetical

Ingredients

Filling Autoclave PackagingFinal Filtration

Other

Formulation

Ingredients

Page 11: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Large Volume Parenterals (LVPs) are single unit doses more than 50 cc. Prefiltration is used for removing particles to

extend the service life of final (sterilizing) filtration. Final filters are used for reducing bioburden or sterile filtration prior

to terminal sterilization. The volume of LVPs is usually tens of thousands of liters, and multiple filling lines may be working

at the same time.

Ingredients in typical LVP solutions include water, dextrose (from 5% to 50%), amino acid, salts and very viscous total

parenteral nutrition (TPN). Prefilters are used to reduce particles for salt solutions, and to remove hard particles for

dextrose solutions before final sterilizing filtration (it's another option to reduce bioburden by using 0.45 μm filters)

www.anowfilter.com9

Large Volume Parenterals (LVP)

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of downstream sterilizing filters

● Final filtration

Reduce bioburden prior to terminal sterilization (0.45 μm)

Sterile filtration prior to terminal sterilization (0.22 μm)

● LVP filters must provide consistent high flow rates to ensure the accuracy and consistency of filling.

● Since typical LVP filling process is operated under high differential pressure and high flow rates, filters must have superior

mechanical strength and be reliable and robust.

● The cost of LVP filters must be economical.

● Prefilters and sterilizing filters must bear multiple cycles of steam-in-place sterilization or hot water sanitization.

Filtration Step Recommendation

Prefiltration LPP, LPPF

Sterile venting LPTA

Final filtration LPS

Separation Goals

Application Requirements

Recommendation

PrefiltrationSterile

Holding

Tank

Final

Filtration

SterileVenting

Mix Tank

Powder

WFI

Filling Autoclave PackagingBioburden

Reduction

www.anowfilter.com 10

Small Volume Parenterals (SVP)

Small volume parenterals (SVP) include various traditional and bioengineered drugs. These drugs are usually packaged in

small vials (less than 20 ml), pre-filled syringes and ampoules, or made in lyophilized powder. Lots of SVPs need aseptic

processing for their lack of heat-stability.

Sterilizing filtration is used after synthesis or before filling. And it can add the sterility assurance if sterilizing filtration is used

at both locations. Prefilters should be used to reduce bioburden and particles, which would clog final filters prematurely.

● Prefiltration

Remove colloidal and particulate contaminants to extend the service life of downstream sterilizing filters

● Final filtration

Provide a sterile filtrate meeting the requirements of current regulatory

Separation Goals

● Final sterilizing filters should remove bacteria without altering the effects of drug products. Therefore, these filters

should have low adsorption of active pharmaceutical ingredient (API), low extractables, be non-pyrogenic and

integrity testable, and be sterile or can be sterilized.

● Prefilters and final filters should have enough flow rates. Final filters in the filling machine must have strong structures

to prevent media flexing during pulsed flow filling processing, which will result in particle release, drips or other

dispense problems.

Filtration Step Recommendation

Prefiltration LPP, LPM

Sterile venting LPTA

Final filtration LPS, LPSD

Application Requirements

Recommendation

PrefiltrationMix Tank

SterileVenting

Active

Pharmacetical

Ingredients

Filling Autoclave PackagingFinal Filtration

Other

Formulation

Ingredients

Page 12: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Ophthalmic preparations, ranging from contact lens cleaning and storing solutions to washing solutions in eye surgery

and eye treatment products, must meet the rigid regulatory requirements and product specifications. The major

component of most ophthalmic solutions is water. Furthermore, there maybe salts such as NaCl, preventatives, vaseline for

the production of ointments and gel polymer used for lubricants. Heat-sensitive ophthalmic solutions can be sterilized by

sterilizing filtration or by adding sterilized components into pre-sterilized bulk solutions.

www.anowfilter.com

Ophthalmic Solutions

● Prefiltration

Reduce particles and bioburden prior to sterilizing filtration

● Sterilizing filtration

Keep reliable retention of microorganisms for a long time

● Filters must provide consistent high flow rates and be robust to satisfy mass manufacturing processes.

● Sterilizing filters must keep reliable retention of microorganisms for a long time.

● Filters must have no adsorption or binding of preservatives in product manufacturing.

Filtration Step Recommendation

Prefiltration LPP, LPM, LPGF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSHV

Separation Goals

Application Requirements

Recommendation

PrefiltrationSterile

Holding

Tank

Final

Filtration

SterileVenting

Mix Tank

Ingredients

WFI

FillingSterile

Filtration

www.anowfilter.com 12

Plasma Fractionation

Human plasma contains lots of valuable therapeutic proteins, such as albumin, a variety of immunoglobulins, VⅢ

ófactors, fibrous proteins and other proteins. The process of extracting and purifying these proteins is called plasma

fractionation. Plasma fractionation is accomplished by a series of extracting and purifying such proteins.

Foreigners in plasma can result in instability of products and clogging of downstream filters. Therefore, prefilters are

necessary for classification and removing impurities prior to chromatography and ultrafiltration. Final filters are used for

the sterilizing filtration of heat-sensitive proteins.

● Prefiltration

Remove colloids, aggregates, non-targeted proteins, lipids and particles to protect sterilizing filters or chromatography

column prior to downstream purification.

● Sterilizing filtration

Control the microorganism level during the manufacturing process.

Final sterile filling (referred to SVPs)

● Prefiltration must remove contaminants and have no retention of target products.

● Filters must have consistent high flow rates and high throughputs for the sake of time and cost.

● Filters should not contaminate feeding liquids, especially metals such as aluminum.

Filtration Step Recommendation

Prefiltration LPM, LPGF, LPPF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSHV

Separation Goals

Recommendation

Application Requirements

ClarificationPrecipitation

Plasma

PrefiltrationVirus Inactivation

SterileVenting

Concentration Final Filtration

11

Page 13: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Ophthalmic preparations, ranging from contact lens cleaning and storing solutions to washing solutions in eye surgery

and eye treatment products, must meet the rigid regulatory requirements and product specifications. The major

component of most ophthalmic solutions is water. Furthermore, there maybe salts such as NaCl, preventatives, vaseline for

the production of ointments and gel polymer used for lubricants. Heat-sensitive ophthalmic solutions can be sterilized by

sterilizing filtration or by adding sterilized components into pre-sterilized bulk solutions.

www.anowfilter.com

Ophthalmic Solutions

● Prefiltration

Reduce particles and bioburden prior to sterilizing filtration

● Sterilizing filtration

Keep reliable retention of microorganisms for a long time

● Filters must provide consistent high flow rates and be robust to satisfy mass manufacturing processes.

● Sterilizing filters must keep reliable retention of microorganisms for a long time.

● Filters must have no adsorption or binding of preservatives in product manufacturing.

Filtration Step Recommendation

Prefiltration LPP, LPM, LPGF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSHV

Separation Goals

Application Requirements

Recommendation

PrefiltrationSterile

Holding

Tank

Final

Filtration

SterileVenting

Mix Tank

Ingredients

WFI

FillingSterile

Filtration

www.anowfilter.com 12

Plasma Fractionation

Human plasma contains lots of valuable therapeutic proteins, such as albumin, a variety of immunoglobulins, VⅢ

ófactors, fibrous proteins and other proteins. The process of extracting and purifying these proteins is called plasma

fractionation. Plasma fractionation is accomplished by a series of extracting and purifying such proteins.

Foreigners in plasma can result in instability of products and clogging of downstream filters. Therefore, prefilters are

necessary for classification and removing impurities prior to chromatography and ultrafiltration. Final filters are used for

the sterilizing filtration of heat-sensitive proteins.

● Prefiltration

Remove colloids, aggregates, non-targeted proteins, lipids and particles to protect sterilizing filters or chromatography

column prior to downstream purification.

● Sterilizing filtration

Control the microorganism level during the manufacturing process.

Final sterile filling (referred to SVPs)

● Prefiltration must remove contaminants and have no retention of target products.

● Filters must have consistent high flow rates and high throughputs for the sake of time and cost.

● Filters should not contaminate feeding liquids, especially metals such as aluminum.

Filtration Step Recommendation

Prefiltration LPM, LPGF, LPPF

Sterile venting LPTA

Final filtration LPS, LPSD, LPSHV

Separation Goals

Recommendation

Application Requirements

ClarificationPrecipitation

Plasma

PrefiltrationVirus Inactivation

SterileVenting

Concentration Final Filtration

11

Page 14: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

LPSL

LPSL filter cartridges are specially designed for sterilizing

filtration of plasma fractionation, lyophilized powder and

vaccines. They are featuring extremely low extractables

with no more than 10mg/10”, longer service life with 40

cycles of SIP. These filters can powerfully ensure final product

quality.

Application

● Plasma Fractionation

● Lyophilized Powder

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch, 30 inch

40 inch

70mm

≥ ( ) per 10-inch cartridge2 20.46m 4.9ft

0.45+0.22

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

Features and Benefits

● Double layer hydrophilic PES Membrane

● Low protein binding

● Extensive drug compatibility for critical applications

● Extremely low extractables

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

www.anowfilter.com

Water bubble point≥ 3500 mbar (50 psig)

Air diffusion ≤ 30ml/min/10”@2.8bar

Low Extractable and Longer Service Life Filter Cartridge with

Double Layer PES Membrane

Bacterial Retention

Extractables

≤ 10 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/cm .

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

40 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

2

14

Bio

ph

arm

ac

eu

tica

l

Ordering Information

SL PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support

PP with stainless

steel endcapB

【 】Code

S

E

V

Silicone

LP D42 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

D42 (0.45+

0.22)μm

【 】Rating【 】Code

SL

End CapConfiguration【 】 Media

【 【

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

(0.22+0.45)μm

0

50

100

150

200

250

300

20 30 40 50

PP with stainless

steel liningC

PPA

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

13

Page 15: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

LPSL

LPSL filter cartridges are specially designed for sterilizing

filtration of plasma fractionation, lyophilized powder and

vaccines. They are featuring extremely low extractables

with no more than 10mg/10”, longer service life with 40

cycles of SIP. These filters can powerfully ensure final product

quality.

Application

● Plasma Fractionation

● Lyophilized Powder

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch, 30 inch

40 inch

70mm

≥ ( ) per 10-inch cartridge2 20.46m 4.9ft

0.45+0.22

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

Features and Benefits

● Double layer hydrophilic PES Membrane

● Low protein binding

● Extensive drug compatibility for critical applications

● Extremely low extractables

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

www.anowfilter.com

Water bubble point≥ 3500 mbar (50 psig)

Air diffusion ≤ 30ml/min/10”@2.8bar

Low Extractable and Longer Service Life Filter Cartridge with

Double Layer PES Membrane

Bacterial Retention

Extractables

≤ 10 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/cm .

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

40 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

2

14

Bio

ph

arm

ac

eu

tica

l

Ordering Information

SL PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support

PP with stainless

steel endcapB

【 】Code

S

E

V

Silicone

LP D42 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

D42 (0.45+

0.22)μm

【 】Rating【 】Code

SL

End CapConfiguration【 】 Media

【 【

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

(0.22+0.45)μm

0

50

100

150

200

250

300

20 30 40 50

PP with stainless

steel liningC

PPA

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

13

Page 16: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSHT Highly Asymmetric PES Filter Cartridge for Higher Throughput Demands

LPSHT filter cartridges are integrity testable membrane

filters, specially developed for terminal filtration needing high

throughputs, such as cell culture media, large volume

parenterals and vaccines applications. They are

characterized by a unique highly asymmetric, hydrophilic

polyethersulfone membrane, offering higher throughputs,

low protein adsorption and superior microbiological safety.

Application

● Cell Culture Medium

● Large Volume Parenterals

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Highly Asymmetric Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2≥ (5.7ft ) per 10-inch cartridge20.53m

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Highly asymmetric, hydrophilic polyethersulfone

membrane

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Ordering Information

16

SHT PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

SHT

End CapConfiguration【 】 Media

【 【

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 7 21 x 10 CFU/cm .

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22μm

0.45μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

15

Page 17: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSHT Highly Asymmetric PES Filter Cartridge for Higher Throughput Demands

LPSHT filter cartridges are integrity testable membrane

filters, specially developed for terminal filtration needing high

throughputs, such as cell culture media, large volume

parenterals and vaccines applications. They are

characterized by a unique highly asymmetric, hydrophilic

polyethersulfone membrane, offering higher throughputs,

low protein adsorption and superior microbiological safety.

Application

● Cell Culture Medium

● Large Volume Parenterals

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Highly Asymmetric Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2≥ (5.7ft ) per 10-inch cartridge20.53m

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Highly asymmetric, hydrophilic polyethersulfone

membrane

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Ordering Information

16

SHT PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

SHT

End CapConfiguration【 】 Media

【 【

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 7 21 x 10 CFU/cm .

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22μm

0.45μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

15

Page 18: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSHV PES Filter Cartridge for Sterile Filtration of High Viscous Pharmacy

LPSHV filter cartridges are designed for terminal filtration,

specially for high viscosity liquids in biopharmaceutical industry,

such as ophthalmic solutions, parenterals and vaccines.

Because of high dirt holding capacity and low protein

adsorption performance, these filters have longer service

life for high viscosity pharmacy filtration.

Application

● Ophthalmic Solution

● Parenterals with High Viscosity(Large Volume

Parenterals, Small Volume Parenterals)

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.53m (5.7ft )

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Low protein binding

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Ordering Information

18

SHV PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

SHV

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

600cp Fluid Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.

1μm

0

100

200

300

400

500

600

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

17

Page 19: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSHV PES Filter Cartridge for Sterile Filtration of High Viscous Pharmacy

LPSHV filter cartridges are designed for terminal filtration,

specially for high viscosity liquids in biopharmaceutical industry,

such as ophthalmic solutions, parenterals and vaccines.

Because of high dirt holding capacity and low protein

adsorption performance, these filters have longer service

life for high viscosity pharmacy filtration.

Application

● Ophthalmic Solution

● Parenterals with High Viscosity(Large Volume

Parenterals, Small Volume Parenterals)

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.53m (5.7ft )

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Low protein binding

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Ordering Information

18

SHV PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

SHV

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

600cp Fluid Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.

1μm

0

100

200

300

400

500

600

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

17

Page 20: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPS Single Layer Hydrophilic PES Filter Cartridge for Final Filtration of Pharmacy

LPS filter cartridges are integrity testable membrane filters

specially developed for sterilizing filtration in

biopharmaceutical industry. They are characterized by a

unique asymmetric, hydrophilic polyethersulfone membrane,

offering high throughputs, low protein adsorption and superior

microbiological safety.

Application

● Active Pharmaceutical Ingredient

● Cell Culture Medium

● Ophthalmic Solution

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Single Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.53m (5.7ft )

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Low protein binding

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

● Plasma Fractionation

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

Ordering Information

20

S PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

S

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.2

2μm

0

50

100

150

200

250

300

20 30 40 50

0.45μm

0.65μm

1.2μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

19

Page 21: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPS Single Layer Hydrophilic PES Filter Cartridge for Final Filtration of Pharmacy

LPS filter cartridges are integrity testable membrane filters

specially developed for sterilizing filtration in

biopharmaceutical industry. They are characterized by a

unique asymmetric, hydrophilic polyethersulfone membrane,

offering high throughputs, low protein adsorption and superior

microbiological safety.

Application

● Active Pharmaceutical Ingredient

● Cell Culture Medium

● Ophthalmic Solution

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Single Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.53m (5.7ft )

0.1, 0.22, 0.45, 0.65, 0.8, 1.2, 3.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85℃ ℃

0.1 μm≥ 3800 mbar (55 psig)

0.22 μm≥ 3400 mbar (49 psig)

0.45 μm≥ 2300 mbar (33 psig)

Features and Benefits

● Low protein binding

● Absolute bacteria retention

● Long service life and high flow rates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

● Plasma Fractionation

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

Ordering Information

20

S PES

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

065

080

120

0.1μm

0.22μm

0.45μm

0.65μm

0.8μm

300

1.2μm

3.0μm

【 】Rating【 】Code

S

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.2

2μm

0

50

100

150

200

250

300

20 30 40 50

0.45μm

0.65μm

1.2μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

19

Page 22: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSD

LPSD filter cartridges are characterized by a unique highly

asymmetric, double-layer hydrophilic polyethersulfone

membrane, specially designed for extremely demanding of

sterilizing filtration in biopharmaceutical industry. These filters

can powerfully ensure products meeting the rigid

requirements of current regulatory.

Application

● Cell Culture Medium

● Ophthalmic Solution

● Plasma Fractionation

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch, 30 inch,

40inch

68mm

≥ 0.44 per 10-inch cartridge2 2m (4.8ft )

0.22+0.1, 0.22+0.22, 0.45+0.22

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.22 μm + 0.1 μm≥ 4000 mbar (58 psig)

0.22 μm + 0.22 μm≥ 3700 mbar (53 psig)

0.45 μm + 0.22 μm≥3500 mbar (50 psig)

Features and Benefits

● Double layer hydrophilic PES membrane

● Low protein binding and extensive drug

compatibility for critical applications

● Integrity testable

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Double Layer Hydrophilic PES Filter Cartridge for

Extremely Demanding of Sterilizing Filtration

Ordering Information

22

S PES

【 】Length【 】Code

05

10

20

30 30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP D22 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

D21

D22

D42

0.22+0.1μm

0.22+0.22μm

0.45+0.22μm

【 】Rating【 】Code

S

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

(0.2

2+0.

1)μm

0

50

100

150

200

250

300

20 30 40 50

(0.2

2+0.

22)μ

m

(0.45+0.22)μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

40 40inch

21

Page 23: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPSD

LPSD filter cartridges are characterized by a unique highly

asymmetric, double-layer hydrophilic polyethersulfone

membrane, specially designed for extremely demanding of

sterilizing filtration in biopharmaceutical industry. These filters

can powerfully ensure products meeting the rigid

requirements of current regulatory.

Application

● Cell Culture Medium

● Ophthalmic Solution

● Plasma Fractionation

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double Layer Hydrophilic PES

Diameter

Length5 inch, 10 inch, 20 inch, 30 inch,

40inch

68mm

≥ 0.44 per 10-inch cartridge2 2m (4.8ft )

0.22+0.1, 0.22+0.22, 0.45+0.22

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.22 μm + 0.1 μm≥ 4000 mbar (58 psig)

0.22 μm + 0.22 μm≥ 3700 mbar (53 psig)

0.45 μm + 0.22 μm≥3500 mbar (50 psig)

Features and Benefits

● Double layer hydrophilic PES membrane

● Low protein binding and extensive drug

compatibility for critical applications

● Integrity testable

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Double Layer Hydrophilic PES Filter Cartridge for

Extremely Demanding of Sterilizing Filtration

Ordering Information

22

S PES

【 】Length【 】Code

05

10

20

30 30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP D22 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

D21

D22

D42

0.22+0.1μm

0.22+0.22μm

0.45+0.22μm

【 】Rating【 】Code

S

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

lPP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

(0.2

2+0.

1)μm

0

50

100

150

200

250

300

20 30 40 50

(0.2

2+0.

22)μ

m

(0.45+0.22)μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

40 40inch

21

Page 24: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPT Hydrophobic PTFE Filter Cartridge with Broad Chemical Compatibility

LPT filter cartridges are characterized by permanently

hydrophobic PTFE membrane, specially developed for

sterile filtration of Active Pharmaceutical Ingredients

production. They are integrity testable, providing high

throughputs, broad chemical compatibility and high flow

rates. Due to their hydrophobic characteristic, they must

be pre-wetted with ethanol or IPA before the filtration of

aqueous solutions.

Features and Benefits

● Broad chemical compatibility

● High throughputs and superior flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

EPDM/Viton/Silicone

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophobic PTFE

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.54 per 10-inch cartridge2 2m (5.8ft )

0.05 0.1, 0.22, 0.45, 1.0,3.0, , 5.0, 10

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

0.1 μm≥ 1000 mbar (14.5 psig)

0.22 μm≥ 900 mbar (13 psig)

0.45 μm≥ 300 mbar (4.35 psig)

Application

● Organic solvent filtration

● Filtration for harsh chemicals and HPLC mobile

phases that destroy other membrane materials

● Sterile filtration for aqueous media

Filtration for strongly corrosive or oxidizing solutions●

Ordering Information

24

T HydrophobicPTFE

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

01K

5.0μm

10μm

【 】Rating【 】Code

T

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

Notes: They must be pre-wetted with ethanol or IPA before the filtration of aqueous solutions.

005 0.05μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

23

Page 25: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPT Hydrophobic PTFE Filter Cartridge with Broad Chemical Compatibility

LPT filter cartridges are characterized by permanently

hydrophobic PTFE membrane, specially developed for

sterile filtration of Active Pharmaceutical Ingredients

production. They are integrity testable, providing high

throughputs, broad chemical compatibility and high flow

rates. Due to their hydrophobic characteristic, they must

be pre-wetted with ethanol or IPA before the filtration of

aqueous solutions.

Features and Benefits

● Broad chemical compatibility

● High throughputs and superior flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

EPDM/Viton/Silicone

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophobic PTFE

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.54 per 10-inch cartridge2 2m (5.8ft )

0.05 0.1, 0.22, 0.45, 1.0,3.0, , 5.0, 10

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

0.1 μm≥ 1000 mbar (14.5 psig)

0.22 μm≥ 900 mbar (13 psig)

0.45 μm≥ 300 mbar (4.35 psig)

Application

● Organic solvent filtration

● Filtration for harsh chemicals and HPLC mobile

phases that destroy other membrane materials

● Sterile filtration for aqueous media

Filtration for strongly corrosive or oxidizing solutions●

Ordering Information

24

T HydrophobicPTFE

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

01K

5.0μm

10μm

【 】Rating【 】Code

T

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

Notes: They must be pre-wetted with ethanol or IPA before the filtration of aqueous solutions.

005 0.05μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

23

Page 26: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPTA filter cartridges are featured by permanently hydrophobic

PTFE membrane, specially designed for sterile venting and gas

application in biopharmaceutical industry. They are integrity

testable, offering the highest process security, high throughputs,

extreme humidity and stringent in-line steam sterilizations

Features and Benefits

● High flow rates and low pressure drop

● High strength, long service life and cost-effective

● 100% integrity testable prior to release

● Have a particulate removal rating of 0.01 m in gases

and a microbial removal rating of 0.22 μm in liquids

μ

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Removal Rating, μm

Maximum Differential Pressure

Integrity Test at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double-layer Polytetrafluoroethylene

(PTFE)

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.54m (5.8ft )

0.01

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

Bubble point≥ 1100 mbar with 60/40% IPA/water(15.95 psig)

HydroCorr (water intrusion test)≤ 0.75mL/min per 10-inch cartridge

with water at 2620mbar

LPTA Hydrophobic PTFE Filter Cartridge for Sterilizing Filtration of Air/Gas

Application

● Sterile venting of vessels and carboys

● Autoclave vacuum break lines

● Fermentation air applications

● Sterile process gases

● Bioreactor inlet and outlet gas filtration

● Sterile filtration of CO2

Ordering Information

TA HydrophobicPTFE for air

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 001 C 1 0

【 】Code 【 】Rating【 】Code

TA

End CapConfiguration【 】 Media

【 【

Extractables

≤ 10 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

200 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

001 0.01μm

26

【 】Code 【 】Support【 】Code

S

E

V

Silicone

BS

【 】Seal

EPDM

Viton

Bacterial Retention

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

TOC

Bio

ph

arm

ac

eu

tica

l

Non-Fiber Releasing

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

30

3Nitrogen Flow Rate(m /h/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0 bar outlet pressure

0

50

100

150

200

250

300

60 90 120 150

2 bar outlet pressure

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

25

Page 27: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPTA filter cartridges are featured by permanently hydrophobic

PTFE membrane, specially designed for sterile venting and gas

application in biopharmaceutical industry. They are integrity

testable, offering the highest process security, high throughputs,

extreme humidity and stringent in-line steam sterilizations

Features and Benefits

● High flow rates and low pressure drop

● High strength, long service life and cost-effective

● 100% integrity testable prior to release

● Have a particulate removal rating of 0.01 m in gases

and a microbial removal rating of 0.22 μm in liquids

μ

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Removal Rating, μm

Maximum Differential Pressure

Integrity Test at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Double-layer Polytetrafluoroethylene

(PTFE)

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.54m (5.8ft )

0.01

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

Bubble point≥ 1100 mbar with 60/40% IPA/water(15.95 psig)

HydroCorr (water intrusion test)≤ 0.75mL/min per 10-inch cartridge

with water at 2620mbar

LPTA Hydrophobic PTFE Filter Cartridge for Sterilizing Filtration of Air/Gas

Application

● Sterile venting of vessels and carboys

● Autoclave vacuum break lines

● Fermentation air applications

● Sterile process gases

● Bioreactor inlet and outlet gas filtration

● Sterile filtration of CO2

Ordering Information

TA HydrophobicPTFE for air

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 001 C 1 0

【 】Code 【 】Rating【 】Code

TA

End CapConfiguration【 】 Media

【 【

Extractables

≤ 10 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

200 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

001 0.01μm

26

【 】Code 【 】Support【 】Code

S

E

V

Silicone

BS

【 】Seal

EPDM

Viton

Bacterial Retention

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

TOC

Bio

ph

arm

ac

eu

tica

l

Non-Fiber Releasing

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

30

3Nitrogen Flow Rate(m /h/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0 bar outlet pressure

0

50

100

150

200

250

300

60 90 120 150

2 bar outlet pressure

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

25

Page 28: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPNN Hydrophilic Nylon Filter Cartridge for Sterile Filtration of Facilities Water & API

LPNN filter cartridges are characterized by hydrophilic

Nylon membrane, providing high throughputs, low

extractables and good mechanical strength, widely used

for sterile filtration in Active Pharmaceutical Ingredients

production and facilities water, for removing particles,

microorganisms and endotoxins to meet the requirements

of FDA and other international standards.

Features and Benefits

● Low extractables and high absorption

● High throughputs and superior flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic Nylon

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.59m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.22 μm≥ 2800 mbar (40.6 psig)

0.45 μm≥ 1200 mbar (17.4 psig)

● Facilities water

● Active pharmaceutical ingredients

Application

Ordering Information

28

NN Nylon

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

【 】Rating【 】Code

NN

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

065 0.65μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.45

μm

0

50

100

150

200

250

300

20 30 40 50

0.2

2μm

1.0μm3.0μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

27

Page 29: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPNN Hydrophilic Nylon Filter Cartridge for Sterile Filtration of Facilities Water & API

LPNN filter cartridges are characterized by hydrophilic

Nylon membrane, providing high throughputs, low

extractables and good mechanical strength, widely used

for sterile filtration in Active Pharmaceutical Ingredients

production and facilities water, for removing particles,

microorganisms and endotoxins to meet the requirements

of FDA and other international standards.

Features and Benefits

● Low extractables and high absorption

● High throughputs and superior flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-Water Bubble Point

at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic Nylon

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ per 10-inch cartridge2 20.59m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

0.22 μm≥ 2800 mbar (40.6 psig)

0.45 μm≥ 1200 mbar (17.4 psig)

● Facilities water

● Active pharmaceutical ingredients

Application

Ordering Information

28

NN Nylon

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

【 】Rating【 】Code

NN

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

065 0.65μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.45

μm

0

50

100

150

200

250

300

20 30 40 50

0.2

2μm

1.0μm3.0μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

27

Page 30: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPTL Hydrophilic PTFE Filter Cartridge for Solvent Filtration

LPTL filter cartridges are characterized by hydrophilic PTFE

membrane and polypropylene components for broad

applications, widely used in Active Pharmaceutical Ingredients

production in a variety of solvent filtration.

Features and Benefits

● Broad chemical compatibility

● No need of pre-wetting

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Viton/EPDM/Silicone

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic Polytetrafluoroethylene

(PTFE)

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.54 per 10-inch cartridge2 2m (5.8ft )

0.1, 0.22, 0.45, 1.0

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

0.1 μm≥1100 mbar (16 psig)

0.22 μm≥ 900 mbar (13 psig)

Application

● Organic solvent filtration

● Filtration for harsh chemicals

● Sterile filtration for aqueous media

Filtration for strongly corrosive or oxidizing solutions●

Ordering Information

30

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

0.1μm

0.22μm

0.45μm

1.0μm

【 】Rating【 】Code

TL

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

TL HydrophilicPTFE

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

29

Page 31: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

LPTL Hydrophilic PTFE Filter Cartridge for Solvent Filtration

LPTL filter cartridges are characterized by hydrophilic PTFE

membrane and polypropylene components for broad

applications, widely used in Active Pharmaceutical Ingredients

production in a variety of solvent filtration.

Features and Benefits

● Broad chemical compatibility

● No need of pre-wetting

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Viton/EPDM/Silicone

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic Polytetrafluoroethylene

(PTFE)

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.54 per 10-inch cartridge2 2m (5.8ft )

0.1, 0.22, 0.45, 1.0

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

0.1 μm≥1100 mbar (16 psig)

0.22 μm≥ 900 mbar (13 psig)

Application

● Organic solvent filtration

● Filtration for harsh chemicals

● Sterile filtration for aqueous media

Filtration for strongly corrosive or oxidizing solutions●

Ordering Information

30

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 022 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

0.1μm

0.22μm

0.45μm

1.0μm

【 】Rating【 】Code

TL

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

TL HydrophilicPTFE

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1

μm

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

29

Page 32: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com31

LPM Hydrophilic MCE Filter Cartridge for Prefiltration of Biologicals

LPM filter cartridges are characterized by high-

performance, hydrophilic mixed cellulose esters

membrane, offering high flow rates, low protein

adsorption and superior microbiological safety.

These filters are designed to reduce costs and are

especially suited for prefiltration of vaccines and

plasma fractionation production.

Features and Benefits

● Low protein binding

● Superior throughputs and cost-effective

● High retention efficiency for more critical

degrees of prefiltration

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic MCE

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.59 per 10-inch cartridge2 2m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

Application

● Vaccines

● Plasma Fractionation

Integrity Test-Water Bubble Point at 23 ℃

0.22μm≥1000 mbar (14.5 psig)

0.45 μm≥ 500 mbar (7.25 psig)

Ordering Information

32

M MCE

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 045 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

【 】Rating【 】Code

M

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

065 0.65μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1μ

m

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 33: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com31

LPM Hydrophilic MCE Filter Cartridge for Prefiltration of Biologicals

LPM filter cartridges are characterized by high-

performance, hydrophilic mixed cellulose esters

membrane, offering high flow rates, low protein

adsorption and superior microbiological safety.

These filters are designed to reduce costs and are

especially suited for prefiltration of vaccines and

plasma fractionation production.

Features and Benefits

● Low protein binding

● Superior throughputs and cost-effective

● High retention efficiency for more critical

degrees of prefiltration

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Membrane

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophilic MCE

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.59 per 10-inch cartridge2 2m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

Application

● Vaccines

● Plasma Fractionation

Integrity Test-Water Bubble Point at 23 ℃

0.22μm≥1000 mbar (14.5 psig)

0.45 μm≥ 500 mbar (7.25 psig)

Ordering Information

32

M MCE

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 045 C 1 0 BS

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

【 】Rating【 】Code

M

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

065 0.65μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.1μ

m

0

50

100

150

200

250

300

20 30 40 50

0.22

μm

0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 34: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com33

LPV Hydrophobic PVDF Filter Cartridge with Low Protein Binding

LPV filter cartridges are characterized by hydrophobic PVDF

membrane and polypropylene components, featuring lowest

protein binding. Due to these characterizes, they are ideal for

sterile filtration of biologicals, chemical intermediates and

organic solvents.

Features and Benefits

● Minimum protein binding and low extractables

● Broad chemical compatibility

● Superior throughputs and high flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/Viton/EPDM

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophobic PVDF

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.59 per 10-inch cartridge2 2m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

0.1 μm≥ 400 mbar (5.8 psig)

0.22 μm≥ 300 mbar (4.35 psig)

Application

● Biologicals

● Chemical intermediates

● Organic solvents

Ordering Information

34

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 045 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

0.1μm

0.22μm

0.45μm

1.0μm

【 】Rating【 】Code

V

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

V HydrophobicPVDF

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

300 3.0μm

500 5.0μm

065 0.65μm

Typical Liquid Flow Rate@23 ℃

2

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.1μm

0

50

100

150

200

250

300

4 6 8 10

0.22μm0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 35: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com33

LPV Hydrophobic PVDF Filter Cartridge with Low Protein Binding

LPV filter cartridges are characterized by hydrophobic PVDF

membrane and polypropylene components, featuring lowest

protein binding. Due to these characterizes, they are ideal for

sterile filtration of biologicals, chemical intermediates and

organic solvents.

Features and Benefits

● Minimum protein binding and low extractables

● Broad chemical compatibility

● Superior throughputs and high flow rates

● 100% integrity testable prior to release

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Integrity Test-60/40% IPA/Water

Bubble Point at 23 ℃

Membrane

Thermal Bonding, No Adhesives

Silicone/Viton/EPDM

PP (222/226 with encapsulated

stainless steel reinforcing ring)

PP

PP

Hydrophobic PVDF

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.59 per 10-inch cartridge2 2m (6.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

0.1 μm≥ 400 mbar (5.8 psig)

0.22 μm≥ 300 mbar (4.35 psig)

Application

● Biologicals

● Chemical intermediates

● Organic solvents

Ordering Information

34

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

【 】Code 【 】Support【 】Code

S

E

V

Silicone

LP 045 C 1 0 BE

【 】Seal

EPDM

Viton

【 】Code

010

022

045

100

0.1μm

0.22μm

0.45μm

1.0μm

【 】Rating【 】Code

V

End CapConfiguration【 】 Media

【 【

Bio

ph

arm

ac

eu

tica

l

V HydrophobicPVDF

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

300 3.0μm

500 5.0μm

065 0.65μm

Typical Liquid Flow Rate@23 ℃

2

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar) 0.1μm

0

50

100

150

200

250

300

4 6 8 10

0.22μm0.45μm

Bacterial Retention

(for 0.1 μm & 0.22 μm only)

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

Effluent Particle Level

Meets the requirements of Chinese Pharmacopoeia

2010, Volume Ⅱ, appendix Ⅸ C.

Non-Fiber Releasing

Meets the criteria for a “non-fiber releasing” filter

as defined in 21 CFR 210.3 (b) (6).

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration of 71 x 10 CFU/ .2cm

TOC

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Multiple Sterilization Cycles

15 steam-in-place sterilization or autoclave cycles of 30

min at 123 ℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010,

volume Ⅱ for purified water.

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 36: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com35

LPP filter cartridges are constructed of polypropylene fine fiber,

featuring high flow rates and high dirt holding capacity. They

are the most economical and efficient prefilters in

biopharmaceutical industry, removing most particulate and

colloidal contaminants. These filters can be personalized

according to your specific fluids and processes, such as pore

size and other characteristics, improving filtration efficiency and

reducing filtration costs.

Features and Benefits

● Superior dirt-holding capacity

● High flow rates

● Broad chemical compatibility

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.41 per 10-inch cartridge2 2m (4.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

LPP The Most Economical PP Filter Cartridge for Prefiltration

Application

● Active Pharmaceutical Ingredient

● Cell Culture Medium

● Ophthalmic Solution

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

● Plasma Fractionation

Ordering Information

P PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

P

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

36

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 80

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

065 0.65μm

01K

02K

10μm

20μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

3.0μm

0

50

100

150

200

250

300

20 30 40 50

0.22μm0.45μm

1.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 37: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com35

LPP filter cartridges are constructed of polypropylene fine fiber,

featuring high flow rates and high dirt holding capacity. They

are the most economical and efficient prefilters in

biopharmaceutical industry, removing most particulate and

colloidal contaminants. These filters can be personalized

according to your specific fluids and processes, such as pore

size and other characteristics, improving filtration efficiency and

reducing filtration costs.

Features and Benefits

● Superior dirt-holding capacity

● High flow rates

● Broad chemical compatibility

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.41 per 10-inch cartridge2 2m (4.4ft )

0.1, 0.22, 0.45, 0.65, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23℃; 1.5 bar @ 85℃

LPP The Most Economical PP Filter Cartridge for Prefiltration

Application

● Active Pharmaceutical Ingredient

● Cell Culture Medium

● Ophthalmic Solution

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

● Plasma Fractionation

Ordering Information

P PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

P

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

36

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 80

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

010

022

045

100

300

500

0.1μm

0.22μm

0.45μm

1.0μm

3.0μm

5.0μm

065 0.65μm

01K

02K

10μm

20μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

3.0μm

0

50

100

150

200

250

300

20 30 40 50

0.22μm0.45μm

1.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 38: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com37

LPPF filter cartridges are constructed of multilayer

polypropylene, featuring high flow rates, broad

chemical compatibility and high dirt holding capacity.

These filters are ideal for prefiltration in

biopharmaceutical industry, removing particulate and

colloidal contaminants. And these cartridges can be

personalized according to your specific filtration fluids

and processes, improving filtration efficiency and

reducing filtration costs.

Features and Benefits

● Superior dirt-holding capacity

● Reliable retention of particulates

● Broad chemical compatibility

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Multi-layer PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2 20.2~0.3 m (2.1~3.2 ft ) per 10-inch element

0.5, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

LPPF The Most Efficient multi-layer PP Filter Cartridge for Prefiltration

Application

● Active Pharmaceutical Ingredients

● Cell Culture Medium

● Ophthalmic Solution

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

● Plasma Fractionation

Ordering Information

PF Multi-layer PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

PF

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

38

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 90

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

100

300

500

1.0μm

3.0μm

5.0μm

050 0.5μm

01K

02K

10μm

20μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.5μ

m

0

50

100

150

200

250

300

20 30 40 50

1.0μm

3.0μm

5.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 39: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com37

LPPF filter cartridges are constructed of multilayer

polypropylene, featuring high flow rates, broad

chemical compatibility and high dirt holding capacity.

These filters are ideal for prefiltration in

biopharmaceutical industry, removing particulate and

colloidal contaminants. And these cartridges can be

personalized according to your specific filtration fluids

and processes, improving filtration efficiency and

reducing filtration costs.

Features and Benefits

● Superior dirt-holding capacity

● Reliable retention of particulates

● Broad chemical compatibility

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Multi-layer PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2 20.2~0.3 m (2.1~3.2 ft ) per 10-inch element

0.5, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85 ℃

LPPF The Most Efficient multi-layer PP Filter Cartridge for Prefiltration

Application

● Active Pharmaceutical Ingredients

● Cell Culture Medium

● Ophthalmic Solution

● Parenterals(Large Volume Parenterals, Small

Volume Parenterals)

● Lyophilized Powder

● Vaccines

● Plasma Fractionation

Ordering Information

PF Multi-layer PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

PF

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

38

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 90

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

100

300

500

1.0μm

3.0μm

5.0μm

050 0.5μm

01K

02K

10μm

20μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.5μ

m

0

50

100

150

200

250

300

20 30 40 50

1.0μm

3.0μm

5.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 40: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com39

LPAP absolute filter cartridges are constructed of

polypropylene fine fiber, featuring high flow rates, high

dirt holding capacity and reliable particle removal

efficiency. Due to their features, they are the most

economical and efficient prefilter cartridges, ideal for

the wide range of classification and prefiltration in

Biopharmaceutical Industry, especially in Active

Pharmaceutical Ingredients Manufacturing.

Features and Benefits

● Superior dirt-holding capacity

● Broad chemical compatibility

● Low extractables and low protein binding

● Reliable retention of particulates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Absolute PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2 20.2~0.3 m (2.1~3.2 ft ) per 10-inch element

0.5, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85℃

LPAP Absolute PP Filter Cartridge for Active Pharmaceutical Ingredients

Application

parenterals, organic solvents, DIW

● Clarification

● Prefiltration for air & gas

Prefiltration for chemical intermediates, biologicals,

Ordering Information

AP PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

AP

End CapConfiguration【 】 Media

【 【

40

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Bio

ph

arm

ac

eu

tica

l

100

300

500

1.0μm

3.0μm

5.0μm

050 0.5μm

01K

02K

10μm

20μm

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 95

TOC

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.5μ

m

0

50

100

150

200

250

300

20 30 40 50

1.0μm

3.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 41: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com39

LPAP absolute filter cartridges are constructed of

polypropylene fine fiber, featuring high flow rates, high

dirt holding capacity and reliable particle removal

efficiency. Due to their features, they are the most

economical and efficient prefilter cartridges, ideal for

the wide range of classification and prefiltration in

Biopharmaceutical Industry, especially in Active

Pharmaceutical Ingredients Manufacturing.

Features and Benefits

● Superior dirt-holding capacity

● Broad chemical compatibility

● Low extractables and low protein binding

● Reliable retention of particulates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Absolute PP

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

2 20.2~0.3 m (2.1~3.2 ft ) per 10-inch element

0.5, 1.0, 3.0, 5.0, 10, 20

Forward: 4.2 bar @ 23 ℃; 1.5 bar @ 85℃

LPAP Absolute PP Filter Cartridge for Active Pharmaceutical Ingredients

Application

parenterals, organic solvents, DIW

● Clarification

● Prefiltration for air & gas

Prefiltration for chemical intermediates, biologicals,

Ordering Information

AP PP

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 100 C 1 0

【 】Code 【 】Rating【 】Code

AP

End CapConfiguration【 】 Media

【 【

40

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Bio

ph

arm

ac

eu

tica

l

100

300

500

1.0μm

3.0μm

5.0μm

050 0.5μm

01K

02K

10μm

20μm

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 95

TOC

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.5μ

m

0

50

100

150

200

250

300

20 30 40 50

1.0μm

3.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 42: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com41

LFGF filter cartridges are adsorption depth filters,

designed for removing colloidal and viscous

contaminants in vaccines and culture media. Featured

by high dirt holding capacity and excellent particle

retention ability, these filters can effectively protect the

final cartridges to extend the service life.

Features and Benefits

● High throughputs and high adsorption

● Superior dirt-holding capacity

● Reliable retention of particulates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Glass Fiber

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.37 per 10-inch element2 2m (4.0ft )

0.45, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

Application

● Vaccines

● Culture Media

● Colloidal and viscous liquids

LPGF Glass Fiber Filter Cartridge for Prefiltration of Viscous Pharmacy and Vaccines

Ordering Information

GF Glass Fiber

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 045 C 1 0

【 】Code 【 】Rating【 】Code

GF

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

42

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 95

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

100

300

500

1.0μm

3.0μm

5.0μm

045 0.45μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.45μm

0

50

100

150

200

250

300

20 30 40 50

1.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 43: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com41

LFGF filter cartridges are adsorption depth filters,

designed for removing colloidal and viscous

contaminants in vaccines and culture media. Featured

by high dirt holding capacity and excellent particle

retention ability, these filters can effectively protect the

final cartridges to extend the service life.

Features and Benefits

● High throughputs and high adsorption

● Superior dirt-holding capacity

● Reliable retention of particulates

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support

Core, Cage and Drainage

End Caps

O-rings/Gasket

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Maximum Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

Silicone/EPDM/Viton

PP

PP

PP

Glass Fiber

Diameter

Length5 inch, 10 inch, 20 inch,

30 inch, 40 inch

68mm

≥ 0.37 per 10-inch element2 2m (4.0ft )

0.45, 1.0, 3.0, 5.0

Forward: 4.2 bar @ 23 ; 1.5 bar @ 85 ℃ ℃

Application

● Vaccines

● Culture Media

● Colloidal and viscous liquids

LPGF Glass Fiber Filter Cartridge for Prefiltration of Viscous Pharmacy and Vaccines

Ordering Information

GF Glass Fiber

【 】Length【 】Code

05

10

20

30

40 40inch

30inch

20inch

10inch

A

B

C

D

222/Fin

222/Flat

226/Fin

226/Flat

DOEE

【 】Code

5inch

LP 045 C 1 0

【 】Code 【 】Rating【 】Code

GF

End CapConfiguration【 】 Media

【 【

Extractables

≤ 50 mg per autoclaved 10-inch cartridge after 24-h soak in purified water at controlled room temperature.

< 500 ppb after a water flush of 60 liters per 10-inch

cartridge.

Sterilization

Support steam-in-place sterilization or autoclave at 123℃.

Oxidizable Substances

Meets the criteria of Chinese Pharmacopoeia 2010, volume Ⅱ

for purified water.

42

【 】Code 【 】Support【 】Code

S

E

V

Silicone

AS

【 】Seal

EPDM

Viton

Particle Removal Efficiency (%)

Toxicity

Component materials meet GB/T 14233.2<2005> of

Chinese National Standard for Safety Tests.

≥ 95

TOC

Bio

ph

arm

ac

eu

tica

l

Bacterial Endotoxins

< 0.25 EU/ml as determined by the LAL test.

100

300

500

1.0μm

3.0μm

5.0μm

045 0.45μm

PP with stainless

steel endcapB

PP with stainless

steel liningC

PPA

Typical Liquid Flow Rate@23 ℃

10

Water Flow Rate(L/min/10")

Dif

fere

nti

al Pre

ssure

(mbar)

0.45μm

0

50

100

150

200

250

300

20 30 40 50

1.0μm

Maximum Operating Temperature

A: PP <60 ℃ (140℉)

B: PP with stainless steel lined end cap <85℃ (185℉)

C: PP with stainless steel lining <95℃ (203℉)

Page 44: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com43

CTP Tri-Clamp capsule filters are designed to provide

smart, disposable and safe filtration for small capacity

liquids of lyophilized powder and other pharmacy. These

disposable filters can help eliminate cleaning problems

and extra validation costs. The T-style configuration is

ideal for operation. 100% integrity testable prior to release

ensures high quality products.

Features and Benefits

● Eco-friendly and cost-effective

● Smart, disposable and safe

● Low hold-up volume

● Good resistance to pressure

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Filtration Area

Pore Size, μm

Maximum Forward Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

PP

PES/Nylon/PTFE/PP/GF/PVDF/MCE

≥ 0.2 2 2m (2.2ft )

Please refer to Ordering Information.

Liquid: 3.5 bar @ 23℃ and 3.0 bar @ 60℃

CTP Tri-Clamp Capsule Filter for Small Volume & High Value-added Pharmacy

Air&Gas: 3.0 bar @ 23℃ and 2.5 bar @ 60℃

Bacterial Retention (for 0.01 μm, 0.1 μm,

0.22 μm PES/PTFE )

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration 7 2of 1 x 10 CFU/cm .

Sterilization

3 autoclave cycles of 30 min at 123 ℃; steam-in-place

sterilization not recommended.

For more information on specification, please refer to cartridges

with the same membrane.

Ordering Information

S PES

【 】Length【 】Code

FS

FE

【 】Code

5inch

CTP 010 FS 5

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

【 【

44

Bio

ph

arm

ac

eu

tica

l

010

022

0.1μm

0.22μm

001 0.01(for air)

μm

NN Nylon

TL HydrophilicPTFE

TA HydrophobicPTFE for Air

T HydrophobicPTFE

P PP

GF Glass Fiber

VHydrophobic

PVDF

100 1.0μm

045 0.45μm

300 3.0μm

5

20

7

∅82.5

∅5

1"TC

mm

Inlet/Outlet: Tri-clampVent&Drain: Silicone

Inlet/Outlet: Tri-clampVent&Drain: EPDM

500 5.0μm

M MCE

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.4 0.8 1.2 1.6 2.0

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

PP PTFE

0.1μm

0.22μm

0.45μm

0.45

μm

1.0μm

3.0μm

Page 45: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com43

CTP Tri-Clamp capsule filters are designed to provide

smart, disposable and safe filtration for small capacity

liquids of lyophilized powder and other pharmacy. These

disposable filters can help eliminate cleaning problems

and extra validation costs. The T-style configuration is

ideal for operation. 100% integrity testable prior to release

ensures high quality products.

Features and Benefits

● Eco-friendly and cost-effective

● Smart, disposable and safe

● Low hold-up volume

● Good resistance to pressure

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Filtration Area

Pore Size, μm

Maximum Forward Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

PP

PES/Nylon/PTFE/PP/GF/PVDF/MCE

≥ 0.2 2 2m (2.2ft )

Please refer to Ordering Information.

Liquid: 3.5 bar @ 23℃ and 3.0 bar @ 60℃

CTP Tri-Clamp Capsule Filter for Small Volume & High Value-added Pharmacy

Air&Gas: 3.0 bar @ 23℃ and 2.5 bar @ 60℃

Bacterial Retention (for 0.01 μm, 0.1 μm,

0.22 μm PES/PTFE )

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration 7 2of 1 x 10 CFU/cm .

Sterilization

3 autoclave cycles of 30 min at 123 ℃; steam-in-place

sterilization not recommended.

For more information on specification, please refer to cartridges

with the same membrane.

Ordering Information

S PES

【 】Length【 】Code

FS

FE

【 】Code

5inch

CTP 010 FS 5

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

【 【

44

Bio

ph

arm

ac

eu

tica

l

010

022

0.1μm

0.22μm

001 0.01(for air)

μm

NN Nylon

TL HydrophilicPTFE

TA HydrophobicPTFE for Air

T HydrophobicPTFE

P PP

GF Glass Fiber

VHydrophobic

PVDF

100 1.0μm

045 0.45μm

300 3.0μm

5

20

7

∅82.5

∅5

1"TC

mm

Inlet/Outlet: Tri-clampVent&Drain: Silicone

Inlet/Outlet: Tri-clampVent&Drain: EPDM

500 5.0μm

M MCE

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.4 0.8 1.2 1.6 2.0

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

PP PTFE

0.1μm

0.22μm

0.45μm

0.45

μm

1.0μm

3.0μm

Page 46: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com45

CHP Hose Barb capsule filters are designed to provide

smart, disposable and safe filtration for small volume

liquid and high value-added liquid of lyophilized

powder and other pharmacy. Disposable filters can

help eliminate cleaning problems and extra validation

costs. 100% integrity testable prior to release ensures

high quality products.

Features and Benefits

● Eco-friendly and cost-effective

● Smart, disposable and safe

● Low hold-up volume

● Good resistance to pressure

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Filtration Area

Pore Size, μm

Maximum Forward Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

PP

PES/Nylon/PTFE/PP/MCE/

PVDF/GF

≥ 0.2 2 2m (2.2ft )

Please refer to Ordering Information.

Liquid: 3.5 bar @ 23℃ and 3.0 bar @ 60℃

CHP Hose Barb Capsule Filter for Small Volume & High Value-added Pharmacy

Air&Gas: 3.0 bar @ 23℃ and 2.5 bar @ 60℃

Bacterial Retention (for 0.01 μm, 0.1 μm,

0.22 μm PES/PTFE )

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration7 2 of 1 x 10 CFU/cm .

Sterilization

3 autoclave cycles of 30 min at 123 ℃; steam-in-place sterilization

not recommended.

For more information on specification, please refer to cartridges

with the same membrane.

Ordering Information

S PES

【 】Length【 】Code

DS

DE

【 】Code

5inch

CHP 022 DS 5

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

【 【

46

Bio

ph

arm

ac

eu

tica

l

010

022

0.1μm

0.22μm

001 0.01(for air)

μm

NN Nylon

TL HydrophilicPTFE

TA HydrophobicPTFE for Air

T HydrophobicPTFE

P PP

GF Glass Fiber

V HydrophobicPVDF

100 1.0μm

045 0.45μm

5

FLOW

Hose barb 13.6mm

∅7.5

189

166

∅70

mm

mm

Inlet/Outlet: 13.6mmVent/Drain: 7.5mmWith Silicone

Inlet/Outlet: 13.6mmVent/Drain: 7.5mmWith EPDM

300 3.0μm

500 5.0μm

M MCE

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.4 0.8 1.2 1.6 2.0

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

PP PTFE

0.1μm

0.22μm

0.45μm

0.45

μm

1.0μm

3.0μm

Page 47: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com45

CHP Hose Barb capsule filters are designed to provide

smart, disposable and safe filtration for small volume

liquid and high value-added liquid of lyophilized

powder and other pharmacy. Disposable filters can

help eliminate cleaning problems and extra validation

costs. 100% integrity testable prior to release ensures

high quality products.

Features and Benefits

● Eco-friendly and cost-effective

● Smart, disposable and safe

● Low hold-up volume

● Good resistance to pressure

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Filtration Area

Pore Size, μm

Maximum Forward Differential Pressure

Filter Media

Thermal Bonding, No Adhesives

PP

PES/Nylon/PTFE/PP/MCE/

PVDF/GF

≥ 0.2 2 2m (2.2ft )

Please refer to Ordering Information.

Liquid: 3.5 bar @ 23℃ and 3.0 bar @ 60℃

CHP Hose Barb Capsule Filter for Small Volume & High Value-added Pharmacy

Air&Gas: 3.0 bar @ 23℃ and 2.5 bar @ 60℃

Bacterial Retention (for 0.01 μm, 0.1 μm,

0.22 μm PES/PTFE )

Passed the bacterial challenge testing using Brevundimonas

diminuta(ATCC19146) at a minimum challenge concentration7 2 of 1 x 10 CFU/cm .

Sterilization

3 autoclave cycles of 30 min at 123 ℃; steam-in-place sterilization

not recommended.

For more information on specification, please refer to cartridges

with the same membrane.

Ordering Information

S PES

【 】Length【 】Code

DS

DE

【 】Code

5inch

CHP 022 DS 5

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

【 【

46

Bio

ph

arm

ac

eu

tica

l

010

022

0.1μm

0.22μm

001 0.01(for air)

μm

NN Nylon

TL HydrophilicPTFE

TA HydrophobicPTFE for Air

T HydrophobicPTFE

P PP

GF Glass Fiber

V HydrophobicPVDF

100 1.0μm

045 0.45μm

5

FLOW

Hose barb 13.6mm

∅7.5

189

166

∅70

mm

mm

Inlet/Outlet: 13.6mmVent/Drain: 7.5mmWith Silicone

Inlet/Outlet: 13.6mmVent/Drain: 7.5mmWith EPDM

300 3.0μm

500 5.0μm

M MCE

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.4 0.8 1.2 1.6 2.0

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min)

PP PTFE

0.1μm

0.22μm

0.45μm

0.45

μm

1.0μm

3.0μm

Page 48: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com47

Features and Benefits

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Thermal Bonding, No Adhesives

PP

Length

Inlet/Outlet Please refer to Ordering Information

2.5”, 5”, 10”

● Compact and sturdy construction

● Disposable design, easy change-out

● High pressure resistance

1/4" NPT Capsule Filter for Small Volume & High Value-added PharmacyCNP

Vent/Drainage Please refer to Ordering Information

2.5- inch

5-inch

10-inch

≥ ( )2 20.1m 1.1ft

Please refer to Ordering Information.

Maximum Operating Pressure

Liquid: 3.5 bar 23℃, 3.0 bar @ 60℃ @

≥ ( )2 20.2m 2.2ft

≥ ( )2 20.3m 3.4ft

Air&Gas: 3.0 bar 23℃, 2.5 bar @ 60℃ @

PES/Nylon/PTFE/PP/GF/PVDF

CNP 1/4"NPT capsule filters are designed to provide

smart, disposable and safe filtration for small volume

liquid and high value-added pharmacy. Disposable

filters can help eliminate cleaning problems and extra

validation costs. 100% integrity testable prior to release

ensures high quality products.

For more information on specification, please refer to cartridges

with the same membrane.

Filter Media

Ordering Information

【 】Length【 】Code

2

5

9 10inch

5inch

【 】Code

2.5inch

CNP 022 B 2

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

Filter 【 【

48

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.2 0.4 0.6 0.8 1.0

0.45μm

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min/2.5")

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min/2.5")

PP PTFE

Inlet/Outlet:1/4"MNPTB

Vent/Drain: 1/8"MNPT

B type connectionH type for pipe threadconnection adapterSilicone O-ring

BHS

B type connectionH type for pipe threadconnection adapter

O-ringEPDM

BHE

010

022

0.1μm

0.22μm

100

045

1.0μm

0.45μm

300

500

3.0μm

5.0μm

0010.01(for air)

μmS PES

NN Nylon

Absolute PP

TLHydrophilic

PTFE

THydrophobic

PTFE

VHydrophobic

PVDF

P PP

TAHydrophobic

PTFE for air

Multi-layer PPPF

AP

GF Glass Fiber

MCEM

NPT1/4"

Ø67

112

H-type adapter

45

29

Ø6

Ø9.3

FLOW

FLOW

Ø67 Ø67

NPT1/4" NPT1/4"

20

1

29

6

FLOW

Unit: mm

0.45μm

0.1

μm

0.2μm

1.0μm

3.0μm

Page 49: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com47

Features and Benefits

Quality

● Cartridges produced in a controlled

environment

● Manufactured according to ISO9001 certified

Quality Management System

Specification

Support & Housing

Sealing Technology

Dimensions

Filtration Area

Pore Size, μm

Thermal Bonding, No Adhesives

PP

Length

Inlet/Outlet Please refer to Ordering Information

2.5”, 5”, 10”

● Compact and sturdy construction

● Disposable design, easy change-out

● High pressure resistance

1/4" NPT Capsule Filter for Small Volume & High Value-added PharmacyCNP

Vent/Drainage Please refer to Ordering Information

2.5- inch

5-inch

10-inch

≥ ( )2 20.1m 1.1ft

Please refer to Ordering Information.

Maximum Operating Pressure

Liquid: 3.5 bar 23℃, 3.0 bar @ 60℃ @

≥ ( )2 20.2m 2.2ft

≥ ( )2 20.3m 3.4ft

Air&Gas: 3.0 bar 23℃, 2.5 bar @ 60℃ @

PES/Nylon/PTFE/PP/GF/PVDF

CNP 1/4"NPT capsule filters are designed to provide

smart, disposable and safe filtration for small volume

liquid and high value-added pharmacy. Disposable

filters can help eliminate cleaning problems and extra

validation costs. 100% integrity testable prior to release

ensures high quality products.

For more information on specification, please refer to cartridges

with the same membrane.

Filter Media

Ordering Information

【 】Length【 】Code

2

5

9 10inch

5inch

【 】Code

2.5inch

CNP 022 B 2

【 】Code 【 】Rating【 】Code

S

Connection【 】 Media

Filter 【 【

48

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate @23 ℃

300

250

200

150

100

50

0 0.2 0.4 0.6 0.8 1.0

0.45μm

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min/2.5")

300

250

200

150

100

50

0 0.5 1.0 1.5 2.0 2.5

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(L/min/2.5")

PP PTFE

Inlet/Outlet:1/4"MNPTB

Vent/Drain: 1/8"MNPT

B type connectionH type for pipe threadconnection adapterSilicone O-ring

BHS

B type connectionH type for pipe threadconnection adapter

O-ringEPDM

BHE

010

022

0.1μm

0.22μm

100

045

1.0μm

0.45μm

300

500

3.0μm

5.0μm

0010.01(for air)

μmS PES

NN Nylon

Absolute PP

TLHydrophilic

PTFE

THydrophobic

PTFE

VHydrophobic

PVDF

P PP

TAHydrophobic

PTFE for air

Multi-layer PPPF

AP

GF Glass Fiber

MCEM

NPT1/4"

Ø67

112

H-type adapter

45

29

Ø6

Ø9.3

FLOW

FLOW

Ø67 Ø67

NPT1/4" NPT1/4"

20

1

29

6

FLOW

Unit: mm

0.45μm

0.1

μm

0.2μm

1.0μm

3.0μm

Page 50: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com49

F5P filters have good pressure resistance up to 350kpa,

2with filtration area of nearly 20 cm .They have high

throughputs under low pressure drops, and can be

reusable after autoclaved. F5P are designed to connect

easily to hose barbs, as well as 6:100 luer slip.

Features and Benefits

Quality

Specification

Support & Housing

Sealing Technology

Dimensions

Filtration Area

Removal Ratings, μm

Filter Media

Thermal Bonding, No Adhesives

PP

Application

Maximum Operating Pressure

Compact and sturdy construction

Good pressure resistance

Disposable design, easy change-out

Filters produced in a controlled environment

Manufactured according to ISO9001 certified

Quality Management System

F5P φ50 Filter Unit

Small-volume venting

Vent device for sensor

Small or medium batch filtration

Outer DiameterΦ65: for PTFE

Inlet/Outlet

Φ60: for PES/Nylon/PP/GF/PVDF/MCE

7~13 mm stepped hose barb connection with 6:100 Luer slip

For more information on specification, please refer to cartridges

with the same membrane.

Please refer to Ordering Information.

≥ ( )2 219.6 cm 0.021 ft

Liquid: 3.5 bar @ 23 ,3.0Bar@ 60℃ ℃

Air&Gas: 3.0 bar @ 23 ,℃ ℃2.5Bar@ 60

PES/Nylon/PTFE/PP/GF/MCE/

PVDF

Ordering Information

【 】Code【 】Code

F5P 022 P 08N

【 】Code 【 】Rating【 】Code

T

Housing【 】

Membrane【 【

50

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate @23 ℃

3000

2500

2000

1500

1000

500

0 100 200 300 400 500

0.22μm

3000

2500

2000

1500

1000

500

010 20 30 40 50

Dif

fere

nti

al Pre

ssure

(mbar)

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(mL/min) Nitrogen Flow Rate(L/min)

0.45μm

0.22μm

PES PTFE

69.8

~70.2

mm

Ø58.6

6:100

6:100

for PES/Nylon/MCE/PP/GF

69.8

~70.2

mm

Ø64.4

6:100

6:100

for PTFE

【 】Prefilter【 】Code

P

None__

PPP

Glass FiberG

08N 8 Non-Sterile

25N

08S

25S

25 Non-Sterile

8 Sterile

25 Sterile

【 】 Packing/

Box(pcs)

P

H

PP

HDPE

010

022

045

0.1μm

0 22. μm

0.45μm

100 1.0μm

S PES

NN Nylon

THydrophobic PTFE

V PVDF

M MCE

GF Glass Fiber

P PP

TAHydrophobic PTFE for Air

TL HydrophilicPTFE for Liquid

0.45μm

Page 51: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com49

F5P filters have good pressure resistance up to 350kpa,

2with filtration area of nearly 20 cm .They have high

throughputs under low pressure drops, and can be

reusable after autoclaved. F5P are designed to connect

easily to hose barbs, as well as 6:100 luer slip.

Features and Benefits

Quality

Specification

Support & Housing

Sealing Technology

Dimensions

Filtration Area

Removal Ratings, μm

Filter Media

Thermal Bonding, No Adhesives

PP

Application

Maximum Operating Pressure

Compact and sturdy construction

Good pressure resistance

Disposable design, easy change-out

Filters produced in a controlled environment

Manufactured according to ISO9001 certified

Quality Management System

F5P φ50 Filter Unit

Small-volume venting

Vent device for sensor

Small or medium batch filtration

Outer DiameterΦ65: for PTFE

Inlet/Outlet

Φ60: for PES/Nylon/PP/GF/PVDF/MCE

7~13 mm stepped hose barb connection with 6:100 Luer slip

For more information on specification, please refer to cartridges

with the same membrane.

Please refer to Ordering Information.

≥ ( )2 219.6 cm 0.021 ft

Liquid: 3.5 bar @ 23 ,3.0Bar@ 60℃ ℃

Air&Gas: 3.0 bar @ 23 ,℃ ℃2.5Bar@ 60

PES/Nylon/PTFE/PP/GF/MCE/

PVDF

Ordering Information

【 】Code【 】Code

F5P 022 P 08N

【 】Code 【 】Rating【 】Code

T

Housing【 】

Membrane【 【

50

Bio

ph

arm

ac

eu

tica

l

Typical Liquid Flow Rate @23 ℃

3000

2500

2000

1500

1000

500

0 100 200 300 400 500

0.22μm

3000

2500

2000

1500

1000

500

010 20 30 40 50

Dif

fere

nti

al Pre

ssure

(mbar)

Dif

fere

nti

al Pre

ssure

(mbar)

Water Flow Rate(mL/min) Nitrogen Flow Rate(L/min)

0.45μm

0.22μm

PES PTFE

69.8

~70.2

mm

Ø58.6

6:100

6:100

for PES/Nylon/MCE/PP/GF69.8

~70.2

mm

Ø64.4

6:100

6:100

for PTFE

【 】Prefilter【 】Code

P

None__

PPP

Glass FiberG

08N 8 Non-Sterile

25N

08S

25S

25 Non-Sterile

8 Sterile

25 Sterile

【 】 Packing/

Box(pcs)

P

H

PP

HDPE

010

022

045

0.1μm

0 22. μm

0.45μm

100 1.0μm

S PES

NN Nylon

THydrophobic PTFE

V PVDF

M MCE

GF Glass Fiber

P PP

TAHydrophobic PTFE for Air

TL HydrophilicPTFE for Liquid

0.45μm

Page 52: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com51

®Easiprep syringe filters are charaterised by various membranes,

diameters, pore sizes and connectors. These filters are disposable,

ideal for clarification, sterile filtration, venting and other demands

in laboratory applications.

®Easiprep φ5/ Syringe Filterφ13/φ20/φ25/φ33

Quality

Application

Filters produced in a controlled environment

Manufactured according to ISO9001 certified

Quality Management System

Clarification and particle removal

Sterile filtration

Venting and gas filtration

Chromatography sample preparation●

Features and Benefits

Low hold-up volume and low extractables

Various inlet/outlet connectors available

Gamma irradiated or EO sterilized

Various membrane diameter available

Broad chemical compatibility

Available in non-sterile and sterile version

52

Bio

ph

arm

ac

eu

tica

l

Ordering Information

【 】Code【 】Code

022 P 08N

【 】Code 【 】Rating【 】Code

T

Housing【 】

Membrane【 【 【 】Prefilter【 】Code

P

None_

PPP

Glass FiberG

1HN 100 Non-Sterile

2HN

50S

1HS

200 Non-Sterile

50 Sterile, EO

100 Sterile, EO

【 】 Packing/

Box(pcs)

P

H

PP

HDPE

010

022

045

0.1μm

0 22. μm

0.45μm

100 1.0μm

S PES

NN Nylon

THydrophobic PTFE

V Hydrophobic PVDF

M MCE

GF Glass Fiber

P PP

TAHydrophobic PTFE for Air

TL Hydrophilic PTFE

B ABS

A

【 】Code 【 】Connection

A

Inlet: female luer lockOutlet: male luer unlock

B

Inlet: male luer unlockOutlet: male luer unlock

C

Inlet: female luer lockOutlet: male luer lock

300 3.0μm

500 5.0μm

【 】Code

S25

Diameter【 】

5

13

5mm

13mm

20 20mm

L

25 25mm

33 33mm

φ13 φ20 φ25 φ33

13 mm 20 mm 25 mm 33 mm

PP/HDPE ABS PP/HDPE PP/HDPE

21.3 cm 23.1 cm 24.9 cm 28.5 cm

16.0mm * 23.0mm 23.0mm*23.5mm 28.0mm*24.3mm 40.0mm*30.3mm

< 100 l μ < 150μl < 250μl < 350μl

Inlet:

Outlet:

131 ℃(267.8℉)

Autoclave at 123℃ at 1 bar for 20 minutes(253.4℉@14.5psi)

< 0.25 EU/ml as determined by the LAL test

Membrane

Diameter

Housing

Filtration

Area

Dimension

Hold-up

Volume

Maximum Operating Temperature

Sterilization

Bacterial Endotoxins

5.2 bar 3.5 bar 5.2bar 5.2 bar

Maximum

Operating

Pressure

Female Luer Lock

Male Luer Slip

Female Luer Lock

Male Luer Lock

Female Luer Lock

Male Luer Slip

Female Luer Lock

Male Luer Lock

Male Luer Slip

Male Luer Slip

Female Luer Lock

Male Luer Slip

Please contact us for more details.

Specification

50S

1HS

50 Sterile, Gamma

100 Sterile, Gamma

φ5

5 mm

PP

20.19 cm

12.0mm * 17.2mm

< 15 l μ

4.0 bar

Female Luer Slip

Male Luer Slip

Page 53: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com51

®Easiprep syringe filters are charaterised by various membranes,

diameters, pore sizes and connectors. These filters are disposable,

ideal for clarification, sterile filtration, venting and other demands

in laboratory applications.

®Easiprep φ5/ Syringe Filterφ13/φ20/φ25/φ33

Quality

Application

Filters produced in a controlled environment

Manufactured according to ISO9001 certified

Quality Management System

Clarification and particle removal

Sterile filtration

Venting and gas filtration

Chromatography sample preparation●

Features and Benefits

Low hold-up volume and low extractables

Various inlet/outlet connectors available

Gamma irradiated or EO sterilized

Various membrane diameter available

Broad chemical compatibility

Available in non-sterile and sterile version

52

Bio

ph

arm

ac

eu

tica

l

Ordering Information

【 】Code【 】Code

022 P 08N

【 】Code 【 】Rating【 】Code

T

Housing【 】

Membrane【 【 【 】Prefilter【 】Code

P

None_

PPP

Glass FiberG

1HN 100 Non-Sterile

2HN

50S

1HS

200 Non-Sterile

50 Sterile, EO

100 Sterile, EO

【 】 Packing/

Box(pcs)

P

H

PP

HDPE

010

022

045

0.1μm

0 22. μm

0.45μm

100 1.0μm

S PES

NN Nylon

THydrophobic PTFE

V Hydrophobic PVDF

M MCE

GF Glass Fiber

P PP

TAHydrophobic PTFE for Air

TL Hydrophilic PTFE

B ABS

A

【 】Code 【 】Connection

A

Inlet: female luer lockOutlet: male luer unlock

B

Inlet: male luer unlockOutlet: male luer unlock

C

Inlet: female luer lockOutlet: male luer lock

300 3.0μm

500 5.0μm

【 】Code

S25

Diameter【 】

5

13

5mm

13mm

20 20mm

L

25 25mm

33 33mm

φ13 φ20 φ25 φ33

13 mm 20 mm 25 mm 33 mm

PP/HDPE ABS PP/HDPE PP/HDPE

21.3 cm 23.1 cm 24.9 cm 28.5 cm

16.0mm * 23.0mm 23.0mm*23.5mm 28.0mm*24.3mm 40.0mm*30.3mm

< 100 l μ < 150μl < 250μl < 350μl

Inlet:

Outlet:

131 ℃(267.8℉)

Autoclave at 123℃ at 1 bar for 20 minutes(253.4℉@14.5psi)

< 0.25 EU/ml as determined by the LAL test

Membrane

Diameter

Housing

Filtration

Area

Dimension

Hold-up

Volume

Maximum Operating Temperature

Sterilization

Bacterial Endotoxins

5.2 bar 3.5 bar 5.2bar 5.2 bar

Maximum

Operating

Pressure

Female Luer Lock

Male Luer Slip

Female Luer Lock

Male Luer Lock

Female Luer Lock

Male Luer Slip

Female Luer Lock

Male Luer Lock

Male Luer Slip

Male Luer Slip

Female Luer Lock

Male Luer Slip

Please contact us for more details.

Specification

50S

1HS

50 Sterile, Gamma

100 Sterile, Gamma

φ5

5 mm

PP

20.19 cm

12.0mm * 17.2mm

< 15 l μ

4.0 bar

Female Luer Slip

Male Luer Slip

Page 54: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com53

Application

Nylon

● Good mechanical strength

● Resistant to alkaline solutions and most

organic solvent

Features

● Alkali

● Organic solvents

● Transfer membrane

Application

PES

Features

● Broad chemical compatibility

● Low protein binding and low extractables

● Terminal filtration

● Environment analysis

Application

MCE

Features

● Low protein binding

● Very suitable for biologics filtration

● Clarification

● Biologics

● Microbiological analysis

● Liquids contain protein

● SDI membrane

Application

PTFE

Features

● Broad chemical compatibility

● Naturally hydrophobic

● Good heat resistance

● Gases

● Organic solvents

● Corrosive liquid

Application

PVDF

Features

● Naturally hydrophobic

● Low protein binding

● Good heat and chemical

resistance

● Gases

● Biologics

● Corrosive liquid

● Transfer membrane

Ordering Information

【 】Code【 】Code

MP 045 293 25

【 】Code 【 】Rating【 】Code

NN

Size【 】

Membrane【 【

54

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

【 】 【 】Code

G

【 】 Packing/

Box(pcs)

Water flow2 rate(ml/cm min

△p=0.1Mpa)20 10 16 4 35 15 30 6 7 3

Sterilization By autoclave at 123 (253.4 ) or EO℃ ℉)

MCE Nylon PES PTFE PVDFMaterial

Pore size

(μm)0.45 0.22 0.45 0.22 0.45 0.22 0.45 0.22 0.45 0.22

Bubble point(mbar)

Water@23 (73.4 )℃ ℉ 60%IPA@23 (73.4 )℃ ℉

150 310 150 310 250 350 60 100 40 70

Thickness

(μm)85-110 90-140 110-140 150-250 90-100

pH 3.5-8.0 6-13 1-14 1-14 2-10

010

022

045

0.1μm

0 22. μm

0.45μm

065 0.65μm

080

120

0 8. μm

1.2μm

300 3.0μm

047

090

142

47mm

90mm

142mm

150 150mm

200

250

200mm

250mm

293 293mm

300 300mm

WithG

WithoutN

NN Nylon

THydrophobic

PTFE

TLHydrophilic

PTFE

M MCE

S PES

V PVDF

25 25

50 50

Interlayer Paper

Page 55: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com53

Application

Nylon

● Good mechanical strength

● Resistant to alkaline solutions and most

organic solvent

Features

● Alkali

● Organic solvents

● Transfer membrane

Application

PES

Features

● Broad chemical compatibility

● Low protein binding and low extractables

● Terminal filtration

● Environment analysis

Application

MCE

Features

● Low protein binding

● Very suitable for biologics filtration

● Clarification

● Biologics

● Microbiological analysis

● Liquids contain protein

● SDI membrane

Application

PTFE

Features

● Broad chemical compatibility

● Naturally hydrophobic

● Good heat resistance

● Gases

● Organic solvents

● Corrosive liquid

Application

PVDF

Features

● Naturally hydrophobic

● Low protein binding

● Good heat and chemical

resistance

● Gases

● Biologics

● Corrosive liquid

● Transfer membrane

Ordering Information

【 】Code【 】Code

MP 045 293 25

【 】Code 【 】Rating【 】Code

NN

Size【 】

Membrane【 【

54

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

【 】 【 】Code

G

【 】 Packing/

Box(pcs)

Water flow2 rate(ml/cm min

△p=0.1Mpa)20 10 16 4 35 15 30 6 7 3

Sterilization By autoclave at 123 (253.4 ) or EO℃ ℉)

MCE Nylon PES PTFE PVDFMaterial

Pore size

(μm)0.45 0.22 0.45 0.22 0.45 0.22 0.45 0.22 0.45 0.22

Bubble point(mbar)

Water@23 (73.4 )℃ ℉ 60%IPA@23 (73.4 )℃ ℉

150 310 150 310 250 350 60 100 40 70

Thickness

(μm)85-110 90-140 110-140 150-250 90-100

pH 3.5-8.0 6-13 1-14 1-14 2-10

010

022

045

0.1μm

0 22. μm

0.45μm

065 0.65μm

080

120

0 8. μm

1.2μm

300 3.0μm

047

090

142

47mm

90mm

142mm

150 150mm

200

250

200mm

250mm

293 293mm

300 300mm

WithG

WithoutN

NN Nylon

THydrophobic

PTFE

TLHydrophilic

PTFE

M MCE

S PES

V PVDF

25 25

50 50

Interlayer Paper

Page 56: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com55

HY series sanitary housings are developed specifically for liquid filtration

in the pharmaceutical, food&beverage, microelectronic and chemical

industry.

● Corrosion resistance and durability with 316L/304 stainless steel

wetted parts and mirror-polished inner and outer surface

● Enhanced cleanability and microbiological safety due to crevice-free,

polished and hygienic design

● Multiple choices for connections

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

● Cost-effective without sacrificing quality and performance

Features and BenefitsSpecification

Maximum Operating Pressure

Series Stainless Steel Filter Housing for Sanitary Liquid FiltrationHY

Operator-friendly and long service life

Low adsorption, easy clean-up and back

washing

No shedding and no leakage

Good heat and corrosion resistance

Suitable for CIP and SIP

-marked●

6bar(87psi)

Maximum Operating Temperature

Cartridge Capacity

1-round, 3-round, 5-round, 7-round, 9-round, 11-round...

Connection

Inlet/Outlet

Gauge Port

Cartridge 222/Fin, 226/Fin, DOE

Flange/ Tri-Clamp

Flange/ Tri-Clamp

Housing

Clamp

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

140℃(284℉)

Ordering Information

【 】Length【 】Code

HY 001 10

【 】Code 【 】 【 】Code

D

【 【

56

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Single-round standard housings

05

10

20

30

225(8.9)

350(13.8)

600(23.6)

850(33.5)

84(3.3)

84(3.3)

84(3.3)

84(3.3)

110(4.3)

110(4.3)

110(4.3)

110(4.3)

CodeCartridge

LengthA B C

127(5)

254(10)

508(20)

762(30)

111.6(4.0)

111.6(4.0)

111.6(4.0)

111.6(4.0)

D

200(7.9)

200(7.9)

200(7.9)

200(7.9)

E

Housing Material

C SUS304

D SUS316L

Cartridge Capacity

001

003

005

009

1

3

5

7

011

9

007

11

10

20

30

40

10inch

20inch

30inch

40inch

【 eal】S【 】Code

T

【 】 【 】Code

C

Connection

A 222/Fin

E DOE

C 226/Fin S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

F

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

20 DN20

Inlet/Outlet Connection

Size

25

38

DN25

DN38

40 DN40

Page 57: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com55

HY series sanitary housings are developed specifically for liquid filtration

in the pharmaceutical, food&beverage, microelectronic and chemical

industry.

● Corrosion resistance and durability with 316L/304 stainless steel

wetted parts and mirror-polished inner and outer surface

● Enhanced cleanability and microbiological safety due to crevice-free,

polished and hygienic design

● Multiple choices for connections

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

● Cost-effective without sacrificing quality and performance

Features and BenefitsSpecification

Maximum Operating Pressure

Series Stainless Steel Filter Housing for Sanitary Liquid FiltrationHY

Operator-friendly and long service life

Low adsorption, easy clean-up and back

washing

No shedding and no leakage

Good heat and corrosion resistance

Suitable for CIP and SIP

-marked●

6bar(87psi)

Maximum Operating Temperature

Cartridge Capacity

1-round, 3-round, 5-round, 7-round, 9-round, 11-round...

Connection

Inlet/Outlet

Gauge Port

Cartridge 222/Fin, 226/Fin, DOE

Flange/ Tri-Clamp

Flange/ Tri-Clamp

Housing

Clamp

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

140℃(284℉)

Ordering Information

【 】Length【 】Code

HY 001 10

【 】Code 【 】 【 】Code

D

【 【

56

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Single-round standard housings

05

10

20

30

225(8.9)

350(13.8)

600(23.6)

850(33.5)

84(3.3)

84(3.3)

84(3.3)

84(3.3)

110(4.3)

110(4.3)

110(4.3)

110(4.3)

CodeCartridge

LengthA B C

127(5)

254(10)

508(20)

762(30)

111.6(4.0)

111.6(4.0)

111.6(4.0)

111.6(4.0)

D

200(7.9)

200(7.9)

200(7.9)

200(7.9)

E

Housing Material

C SUS304

D SUS316L

Cartridge Capacity

001

003

005

009

1

3

5

7

011

9

007

11

10

20

30

40

10inch

20inch

30inch

40inch

【 eal】S【 】Code

T

【 】 【 】Code

C

Connection

A 222/Fin

E DOE

C 226/Fin S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

F

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

20 DN20

Inlet/Outlet Connection

Size

25

38

DN25

DN38

40 DN40

Page 58: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Cartridge Capacity

Connection

Inlet/Outlet

Gauge Port

Cartridge 222/Fin, 226/Fin, DOE

Flange/ Tri-Clamp

Flange/ Tri-Clamp

Housing

Clamp

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

www.anowfilter.com57

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HK Series Stainless Steel Filter Housing for Gas&Air Filtration

HK series sanitary housings are developed specifically for gas&air

filtration in

● Corrosion resistance and durability with 316L/304 stainless steel

wetted parts and mirror-polished inner and outer surface

● Enhanced cleanability and microbiological safety due to

crevice-free, polished and hygienic design

● Multiple choices for connections

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

● Cost-effective without sacrificing quality and performance

pharmaceutical, food&beverage, microelectronic and

chemical industry.

Operator-friendly and long service life

Low adsorption

Mirror-polished inner and outer surface

No shedding and no leakage

-marked●

1-round, 3-round, 5-round, ...

Ordering Information

【 】Length【 】Code

HK 001 10

【 】Code 【 】 【 】Code

D

【 【

58

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

Cartridge Capacity

001

003

005

009

1

3

5

7

011

9

007

11

10

20

30

40

10inch

20inch

30inch

40inch

【 eal】S【 】Code

T

【 】 【 】Code

C

Connection

A 222/Fin

E DOE

C 226/Fin S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

F

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

20 DN20

Inlet/Outlet Connection

Size

25 DN25

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

05

10

20

30

40

185(7.3)

310(2.2)

560(22.0)

810(31.9)

1060(41.7)

75(3.0)

75(3.0)

75(3.0)

75(3.0)

75(3.0)

158(6.2)

158(6.2)

158(6.2)

158(6.2)

158(6.2)

Code Cartridge Length A B C

127(5)

254(10)

508(20)

762(30)

1016(40)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

D

250(9.8)

250(9.8)

250(9.8)

250(9.8)

250(9.8)

E

20(0.8)

20(0.8)

20(0.8)

20(0.8)

20(0.8)

F

20(0.8)

20(0.8)

20(0.8)

20(0.8)

20(0.8)

G

5 5inch

Page 59: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Cartridge Capacity

Connection

Inlet/Outlet

Gauge Port

Cartridge 222/Fin, 226/Fin, DOE

Flange/ Tri-Clamp

Flange/ Tri-Clamp

Housing

Clamp

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

www.anowfilter.com57

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HK Series Stainless Steel Filter Housing for Gas&Air Filtration

HK series sanitary housings are developed specifically for gas&air

filtration in

● Corrosion resistance and durability with 316L/304 stainless steel

wetted parts and mirror-polished inner and outer surface

● Enhanced cleanability and microbiological safety due to

crevice-free, polished and hygienic design

● Multiple choices for connections

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

● Cost-effective without sacrificing quality and performance

pharmaceutical, food&beverage, microelectronic and

chemical industry.

Operator-friendly and long service life

Low adsorption

Mirror-polished inner and outer surface

No shedding and no leakage

-marked●

1-round, 3-round, 5-round, ...

Ordering Information

【 】Length【 】Code

HK 001 10

【 】Code 【 】 【 】Code

D

【 【

58

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

Cartridge Capacity

001

003

005

009

1

3

5

7

011

9

007

11

10

20

30

40

10inch

20inch

30inch

40inch

【 eal】S【 】Code

T

【 】 【 】Code

C

Connection

A 222/Fin

E DOE

C 226/Fin S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

F

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

20 DN20

Inlet/Outlet Connection

Size

25 DN25

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

05

10

20

30

40

185(7.3)

310(2.2)

560(22.0)

810(31.9)

1060(41.7)

75(3.0)

75(3.0)

75(3.0)

75(3.0)

75(3.0)

158(6.2)

158(6.2)

158(6.2)

158(6.2)

158(6.2)

Code Cartridge Length A B C

127(5)

254(10)

508(20)

762(30)

1016(40)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

D

250(9.8)

250(9.8)

250(9.8)

250(9.8)

250(9.8)

E

20(0.8)

20(0.8)

20(0.8)

20(0.8)

20(0.8)

F

20(0.8)

20(0.8)

20(0.8)

20(0.8)

20(0.8)

G

5 5inch

Page 60: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Connection

Inlet/Outlet Flange/ Tri-Clamp

www.anowfilter.com59

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HM Series Filter Sanitary Disc Holder

HM series sanitary housings are developed specifically for

liquid and gas filtration in the

Corrosion resistance and durability with 316L/304

stainless steel wetted parts and mirror-polished inner

and outer surface

PTFE lining is available to provide advanced protection

from corrosion

pharmaceutical, food&beverage,

microelectronic and chemical industry.

Long service life

Low adsorption

Easy installation, clean up, and adjustment

No shedding and no leakage

Good heat and corrosion resistance

-marked●

Housing

Membrane Diameter

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

47mm, 90mm, 100mm, 142mm, 150mm, 293mm

Ordering Information

HM 293

【 】Code 【 】 【 】Code

D

【 【

60

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

FilterDiameter 【 eal】S【 】Code

S

【 】 【 】Code

A

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet Connection

Size

A

B

1

2

Layers

293mm Disc Filter Holder

293 294(11.5) 15(0.6) 15(0.6) 150(5.9)

Code Membrane Diameter A C D E

293(11.5) 360(14.2)

B

047

090

100

150

47

90

100

142

293

150

142

293

15 DN15

20 DN20

25 DN25

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Page 61: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Connection

Inlet/Outlet Flange/ Tri-Clamp

www.anowfilter.com59

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HM Series Filter Sanitary Disc Holder

HM series sanitary housings are developed specifically for

liquid and gas filtration in the

Corrosion resistance and durability with 316L/304

stainless steel wetted parts and mirror-polished inner

and outer surface

PTFE lining is available to provide advanced protection

from corrosion

pharmaceutical, food&beverage,

microelectronic and chemical industry.

Long service life

Low adsorption

Easy installation, clean up, and adjustment

No shedding and no leakage

Good heat and corrosion resistance

-marked●

Housing

Membrane Diameter

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

47mm, 90mm, 100mm, 142mm, 150mm, 293mm

Ordering Information

HM 293

【 】Code 【 】 【 】Code

D

【 【

60

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

FilterDiameter 【 eal】S【 】Code

S

【 】 【 】Code

A

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet Connection

Size

A

B

1

2

Layers

293mm Disc Filter Holder

293 294(11.5) 15(0.6) 15(0.6) 150(5.9)

Code Membrane Diameter A C D E

293(11.5) 360(14.2)

B

047

090

100

150

47

90

100

142

293

150

142

293

15 DN15

20 DN20

25 DN25

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Page 62: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Connection

www.anowfilter.com61

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HT Series Titanium Filter Housing

HT series sanitary housings are developed for liquid filtration in

the pharmaceutical, food and beverage, microelectronic industry,

especially suitable for carbon removal, high temperature and

corrosive liquid filtration in infusion and injection manufacturing.

● Corrosion resistance and durability with 316L/304 stainless

steel wetted parts and mirror-polished inner and outer surface

● Use titanium powder sintered filter

● Side-in and down-out structure, with multiple choices for inlet

and outlet connections

● Easy clean up and backwash

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

Long service life

Low adsorption

No shedding and no leakage

Good corrosion and acid and alkali resistance

Titanium filter is reusable

-marked●

Housing

Clamp

Cartridge Capacity

1-round, 3-round, 5-round, 7-round, 9-round, 11-round

Inlet/Outlet

Cartridge

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

Flange/ Tri-Clamp

316L/304 stainless steel

Gauge Port Flange/ Tri-Clamp

M20/M30 Thread

Ordering Information

HT 011

【 】Code 【 】 【 】Code

D

【 【

62

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

Cartridge Capacity 【 eal】S【 】Code

S

【 】 【 】Code

M2

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet Connection

SizeConnection

25 DN25

38 DN38

40 DN40

M2

M3

M20

M30

10

20

30

40

10inch

20inch

30inch

40inch

5-Round standard housing of 20”

20 508(20) 440(17.3) 420(16.5) 200(7.9)

CodeCartridge

HeightA B C D E

200(7.9) 290(11.4)

F

14(0.6)

G

14(0.6)

H

121(4.8)

001

003

005

009

1

3

5

7

011

9

007

11

013 13

【 】Length【 】Code

10

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

50 DN50

Page 63: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and Benefits Specification

Connection

www.anowfilter.com61

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

HT Series Titanium Filter Housing

HT series sanitary housings are developed for liquid filtration in

the pharmaceutical, food and beverage, microelectronic industry,

especially suitable for carbon removal, high temperature and

corrosive liquid filtration in infusion and injection manufacturing.

● Corrosion resistance and durability with 316L/304 stainless

steel wetted parts and mirror-polished inner and outer surface

● Use titanium powder sintered filter

● Side-in and down-out structure, with multiple choices for inlet

and outlet connections

● Easy clean up and backwash

● Single-round and multi-round filter housings are available with

cartridges of 10/ 20/ 30/ 40 inch

Long service life

Low adsorption

No shedding and no leakage

Good corrosion and acid and alkali resistance

Titanium filter is reusable

-marked●

Housing

Clamp

Cartridge Capacity

1-round, 3-round, 5-round, 7-round, 9-round, 11-round

Inlet/Outlet

Cartridge

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

Flange/ Tri-Clamp

316L/304 stainless steel

Gauge Port Flange/ Tri-Clamp

M20/M30 Thread

Ordering Information

HT 011

【 】Code 【 】 【 】Code

D

【 【

62

Bio

ph

arm

ac

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tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Housing Material

C SUS304

D SUS316L

Cartridge Capacity 【 eal】S【 】Code

S

【 】 【 】Code

M2

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet Connection

SizeConnection

25 DN25

38 DN38

40 DN40

M2

M3

M20

M30

10

20

30

40

10inch

20inch

30inch

40inch

5-Round standard housing of 20”

20 508(20) 440(17.3) 420(16.5) 200(7.9)

CodeCartridge

HeightA B C D E

200(7.9) 290(11.4)

F

14(0.6)

G

14(0.6)

H

121(4.8)

001

003

005

009

1

3

5

7

011

9

007

11

013 13

【 】Length【 】Code

10

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

50 DN50

Page 64: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and BenefitsSpecification

Connection

www.anowfilter.com63

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

Cartridge Capacity

Fast filtration, long service life

Mirror-polished inner and outer surface

Low adsorption, no shedding and no leakage

-marked●

HG Series Sanitary In-line Liquid and Gas Filter Housing

HG series sanitary housings are developed specifically for liquid filtration

in the

such as pure water, ultra pure water, drinking water, distilled water,

acid and alkali, and other chemicals.

Corrosion resistance and durability with 316L/304 stainless steel wetted

parts and mirror-polished inner and outer surface

Enhanced cleanability and microbiological safety due to

crevice-free, polished and hygienic design

Multiple choices for inlet and outlet connections

Single-round and multi-round filter housings are available

pharmaceutical, food&beverage, microelectronic and chemical

industry

Housing

Clamp

1-round, 3-round, 5-round

Inlet/Outlet

Cartridge

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

Flange/ Tri-Clamp

222/Fin, 226/Fin, DOE

Ordering Information

64

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Single-round standard housings

05

10

20

30

127(5)

254(10)

508(20)

762(30)

225(8.9)

350(13.8)

600(23.6)

850(33.5)

44(1.7)

44(1.7)

44(1.7)

44(1.7)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

Code Cartridge Length A B D

HG 001

【 】Code 【 】 【 】Code

D

【 【Housing Material

C SUS304

D SUS316L

Cartridge Capacity 【 eal】S【 】Code

S

【 】 【 】Code

C

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet

Connection Size

Connection

10

20

30

10inch

20inch

30inch

001

003

005

009

1

3

5

7

011

9

007

11

【 】Length【 】Code

10

A

C

222/Fin

226/Fin

5 5inch DN15

20 DN

25

38

40

15

20

DN 25

DN 38

DN 40

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Page 65: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

Features and BenefitsSpecification

Connection

www.anowfilter.com63

Maximum Operating Pressure

6bar(87psi)

140℃(284℉)

Maximum Operating Temperature

Cartridge Capacity

Fast filtration, long service life

Mirror-polished inner and outer surface

Low adsorption, no shedding and no leakage

-marked●

HG Series Sanitary In-line Liquid and Gas Filter Housing

HG series sanitary housings are developed specifically for liquid filtration

in the

such as pure water, ultra pure water, drinking water, distilled water,

acid and alkali, and other chemicals.

Corrosion resistance and durability with 316L/304 stainless steel wetted

parts and mirror-polished inner and outer surface

Enhanced cleanability and microbiological safety due to

crevice-free, polished and hygienic design

Multiple choices for inlet and outlet connections

Single-round and multi-round filter housings are available

pharmaceutical, food&beverage, microelectronic and chemical

industry

Housing

Clamp

1-round, 3-round, 5-round

Inlet/Outlet

Cartridge

Seal Silicone/EPDM/Viton/TEV

316L/304 stainless steel

304 stainless steel

Flange/ Tri-Clamp

222/Fin, 226/Fin, DOE

Ordering Information

64

Bio

ph

arm

ac

eu

tica

l

This information is a guide to the Part No. structure and possible options. For availability of specific options and housing

details, please contact ANOW.

Single-round standard housings

05

10

20

30

127(5)

254(10)

508(20)

762(30)

225(8.9)

350(13.8)

600(23.6)

850(33.5)

44(1.7)

44(1.7)

44(1.7)

44(1.7)

101.6(4.0)

101.6(4.0)

101.6(4.0)

101.6(4.0)

Code Cartridge Length A B D

HG 001

【 】Code 【 】 【 】Code

D

【 【Housing Material

C SUS304

D SUS316L

Cartridge Capacity 【 eal】S【 】Code

S

【 】 【 】Code

C

S

E EPDM

V Viton

T TEV

Silicone

【 】 【 】Code

K

Inlet/ Outlet

K Tri-Clamp

F Flange

【 】 【 】Code

25

Inlet/Outlet

Connection Size

Connection

10

20

30

10inch

20inch

30inch

001

003

005

009

1

3

5

7

011

9

007

11

【 】Length【 】Code

10

A

C

222/Fin

226/Fin

5 5inch DN15

20 DN

25

38

40

15

20

DN 25

DN 38

DN 40

Nominal Dimensions in mm(inches)-for specific dimensions, please contact ANOW.

Page 66: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com65

Chemical Compatibility Guide

Classification Name Nylon PVDF PTFE PES PP MCE Silicone EPDM Viton TEV

Acids

Acetic Acid NR R R NR R LR LR R NR R

Hydrochloric Acid (conc.) NR R R R R NR NR NR NR R

Hydrochloric Acid (6N) NR R R R R NR NR NR R R

Nitric Acid (conc.) NR R R - R NR NR NR R R

Nitric Acid (6N) NR R R - R NR LR NR R R

Phosphoric Acid (conc.) NR R R - R NR NR R R R

Sulfuric Acid (conc.) NR R R NR R NR NR NR R R

Hydrofluoric Acid (6N) NR R R - NR NR NR NR - R

Bases

Ammonium Hydroxide (1N) R LR R R R R R R R R

Ammonium Hydroxide (3N) R NR R R R NR R LR LR R

Potassium Hydroxide (3N) R LR R R R NR LR R R R

Sodium Hydroxide (3N) R LR R R R NR R R R R

Sodium Hydroxide (6N) R NR R R R NR R R R R

Alcohols

Amyl Alcohol R R R R R NR NR R R R

Benzyl Alcohol (100%) R R R R R NR LR R R R

Butanol R R R R R R R R LR R

Isopropanol R R R R R - R R R R

Methanol LR R R R R LR R R NR R

Ketones

Acetone R LR R NR R NR NR R NR R

Cyclohexanone - LR R NR R NR NR NR NR R

Methyl Ethyl Ketone LR LR R - R - NR R NR R

Methyl Isobutyl Ketone LR LR R NR R - NR R NR R

Oils

Cottonseed R R R - R - R R R

Lubricant R R R NR R - R R R R

Peanut R R R - R - R R R R

Sesame R R R R R - R R R R

Aromatic

Hydrocarbons

Benzene LR LR R LR NR R NR NR R R

Toluene NR LR R NR NR R NR NR R R

Xylene LR LR R NR NR R NR NR R R

Halogenated

Hydrocarbons

Carbon Tetrachloride LR LR R LR LR NR NR NR R R

Chloroform LR LR R NR LR NR NR NR R R

Ethylene Dichloride LR LR R NR LR R NR NR LR R

Freon TF R R R R LR R NR NR R R

Freon TMC LR LR R NR LR R NR NR LR R

Methylene Dichloride NR LR R NR LR NR NR NR LR R

Perchloroethylene - LR R LR LR R NR NR R R

Trichloroethylene LR NR R LR LR R NR NR R R

Bio

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66

Glycols

Ethylene Glycol R R R LR R - R R R R

Glycerol R R R LR R R R R R R

Propylene Glycol R R R LR R R R R

Ethers

Ethyl Ether NR R R R LR NR LR NR NR R

Isopropyl Ether - R R - R NR NR NR NR R

Dioxane R R R - R NR NR NR NR R

Tetrahydrofuran NR LR R NR LR NR NR NR NR R

Esters

Amyl Acetate LR R R - R NR NR R NR R

Butyl Acetate LR R R - LR NR NR R R R

Cellosolve Acetate - R R R R NR NR R NR R

Ethyl Acetate LR R R LR LR NR R R R R

Methyl Acetate LR R R NR R NR - R R R

Isopropyl Acetate - R R R R NR LR R NR R

Classification Name Nylon PVDF PTFE PES PP MCE Silicone EPDM Viton TEV

Connections

Aniline LR R R NR LR - NR R R R

Dimethyl Formamide R NR R NR R - R R NR R

Formaldehyde (37%) R R R R R - R R NR R

Gasoline LR LR LR R LR R NR R R R

Hexane (dry) - LR LR LR LR R NR NR R R

Kerosene - R R R R - NR NR R R

Phenol R R R NR R R NR NR R R

Pyridine LR R R NR LR NR NR R NR R

Turpentine - R R R LR - NR NR R R

Water R R R R R R LR R R R

Acetonitrile LR R R R LR NR - R NR R

Nickel Sulfate Solution R R R - R - R R - R

Notes: This table is intended to serve as a guide only. Accuracy cannot be guaranteed. Users are responsible

for verifying chemical compatibility under their own conditions of use. Chemical compatibility is affected by

many variables including temperature, pressure, concentration, and chemical purity.

R: Resistance;

LR: Limited resistance;

NR: No resistance;

“-”: No data available.

R

Miscellaneous

222/Fin 222/Flat 226/Fin 226/Flat DOE

Page 67: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com65

Chemical Compatibility Guide

Classification Name Nylon PVDF PTFE PES PP MCE Silicone EPDM Viton TEV

Acids

Acetic Acid NR R R NR R LR LR R NR R

Hydrochloric Acid (conc.) NR R R R R NR NR NR NR R

Hydrochloric Acid (6N) NR R R R R NR NR NR R R

Nitric Acid (conc.) NR R R - R NR NR NR R R

Nitric Acid (6N) NR R R - R NR LR NR R R

Phosphoric Acid (conc.) NR R R - R NR NR R R R

Sulfuric Acid (conc.) NR R R NR R NR NR NR R R

Hydrofluoric Acid (6N) NR R R - NR NR NR NR - R

Bases

Ammonium Hydroxide (1N) R LR R R R R R R R R

Ammonium Hydroxide (3N) R NR R R R NR R LR LR R

Potassium Hydroxide (3N) R LR R R R NR LR R R R

Sodium Hydroxide (3N) R LR R R R NR R R R R

Sodium Hydroxide (6N) R NR R R R NR R R R R

Alcohols

Amyl Alcohol R R R R R NR NR R R R

Benzyl Alcohol (100%) R R R R R NR LR R R R

Butanol R R R R R R R R LR R

Isopropanol R R R R R - R R R R

Methanol LR R R R R LR R R NR R

Ketones

Acetone R LR R NR R NR NR R NR R

Cyclohexanone - LR R NR R NR NR NR NR R

Methyl Ethyl Ketone LR LR R - R - NR R NR R

Methyl Isobutyl Ketone LR LR R NR R - NR R NR R

Oils

Cottonseed R R R - R - R R R

Lubricant R R R NR R - R R R R

Peanut R R R - R - R R R R

Sesame R R R R R - R R R R

Aromatic

Hydrocarbons

Benzene LR LR R LR NR R NR NR R R

Toluene NR LR R NR NR R NR NR R R

Xylene LR LR R NR NR R NR NR R R

Halogenated

Hydrocarbons

Carbon Tetrachloride LR LR R LR LR NR NR NR R R

Chloroform LR LR R NR LR NR NR NR R R

Ethylene Dichloride LR LR R NR LR R NR NR LR R

Freon TF R R R R LR R NR NR R R

Freon TMC LR LR R NR LR R NR NR LR R

Methylene Dichloride NR LR R NR LR NR NR NR LR R

Perchloroethylene - LR R LR LR R NR NR R R

Trichloroethylene LR NR R LR LR R NR NR R R

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66

Glycols

Ethylene Glycol R R R LR R - R R R R

Glycerol R R R LR R R R R R R

Propylene Glycol R R R LR R R R R

Ethers

Ethyl Ether NR R R R LR NR LR NR NR R

Isopropyl Ether - R R - R NR NR NR NR R

Dioxane R R R - R NR NR NR NR R

Tetrahydrofuran NR LR R NR LR NR NR NR NR R

Esters

Amyl Acetate LR R R - R NR NR R NR R

Butyl Acetate LR R R - LR NR NR R R R

Cellosolve Acetate - R R R R NR NR R NR R

Ethyl Acetate LR R R LR LR NR R R R R

Methyl Acetate LR R R NR R NR - R R R

Isopropyl Acetate - R R R R NR LR R NR R

Classification Name Nylon PVDF PTFE PES PP MCE Silicone EPDM Viton TEV

Connections

Aniline LR R R NR LR - NR R R R

Dimethyl Formamide R NR R NR R - R R NR R

Formaldehyde (37%) R R R R R - R R NR R

Gasoline LR LR LR R LR R NR R R R

Hexane (dry) - LR LR LR LR R NR NR R R

Kerosene - R R R R - NR NR R R

Phenol R R R NR R R NR NR R R

Pyridine LR R R NR LR NR NR R NR R

Turpentine - R R R LR - NR NR R R

Water R R R R R R LR R R R

Acetonitrile LR R R R LR NR - R NR R

Nickel Sulfate Solution R R R - R - R R - R

Notes: This table is intended to serve as a guide only. Accuracy cannot be guaranteed. Users are responsible

for verifying chemical compatibility under their own conditions of use. Chemical compatibility is affected by

many variables including temperature, pressure, concentration, and chemical purity.

R: Resistance;

LR: Limited resistance;

NR: No resistance;

“-”: No data available.

R

Miscellaneous

222/Fin 222/Flat 226/Fin 226/Flat DOE

Page 68: Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and gas & air filtration solutions for customers around the world in biopharmaceutical,

www.anowfilter.com

Biopharmaceutical

Filtration Solutions

Hangzhou Anow Microfiltraion Co.,Ltd.Office:Room 901-903, Central Building, No.271, Hushu South Road, Hangzhou, China

Plant: Qingming Bridge, Xindeng Industrial Zone, Fuyang, Hangzhou, China

Tel: +86-571-883-70389

Fax: +86-571-883-70399

Website: www.anowfilter.com

E-mail: [email protected]

Making the Filtration Better