Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and...
Transcript of Biopharmaceutical Filtration Solutions · filters. provides professional assistances to liquid and...
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
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
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
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
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
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.
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.
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
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
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
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
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
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
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
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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
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
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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℉)
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
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
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
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
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
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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
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
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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
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
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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
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
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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
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
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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
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
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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
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
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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
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
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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
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
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arm
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eu
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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
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
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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
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
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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
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
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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
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.
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.
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
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
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.
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
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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.
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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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
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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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
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