7S Chan Tsz Wa 7S Li Wing Tung Drug Development...
Transcript of 7S Chan Tsz Wa 7S Li Wing Tung Drug Development...
![Page 1: 7S Chan Tsz Wa 7S Li Wing Tung Drug Development Ibuprofenaerodrive.ccchwc.edu.hk/~lck/1011_7s/10117sgp04ppt.pdf · 2010. 10. 17. · later called ibuprofen. 1961 1964 further development.](https://reader033.fdocuments.net/reader033/viewer/2022060911/60a5df68d217611be24de86f/html5/thumbnails/1.jpg)
7S Chan Tsz Wa
7S Li Wing Tung
Drug Development
Ibuprofen
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Introduction
• an anti-inflammatory drug
• NSAID
• possesses pain-relieving and
fever-reducing properties.
• particular use in pain relief from arthritis
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Introduction (cont’d)
• 2D Structure of Ibuprofen
• 3D Structure of Ibuprofen
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Principle
Arachidonic acid Prostaglandin
Inhibited
by
NASIDs
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Lead compound discovery
• developed and discovered as a
drug by the Boots Company.
• 2-methylpropylbenzene
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Timeline
1955
� The discovery was made.
� anti-inflammatory drugs
� simple screening test for new chemicalcompounds
� Research was started.
Aspirin and phenylbutazone were available.Objective: 1.To develop a drug to treat rheumatoid arthritis (inflamed joints) 2.To have a superior profile both in terms of potency and toxicity to these two drugs.
1956
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Timeline (cont’d)
1958
� compound code named BTS 8402 is given aclinical trial (i.e. a trial on patients).
� no better than aspirin.
� A patent is filed for the compound 2-(4-isobutylphenyl) propanoic acid
� later called ibuprofen.
1961
� further development1964
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Timeline (cont’d)
1966
� Northern General Hospital in Edinburgh
� anti-inflammatory effect in patients
� Clinical trials of Ibuprofen are launched inthe UK on prescription only.
1969
� available without prescription.1983
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Organic synthesis
� A) The original Boots synthesis of ibuprofen
Step1
Friedel-Crafts acetylation
of 2-methylpropylbenzene
Step2
Reaction with ethyl chloroacetate
(Darzens reaction) gave the
α,β-epoxy ester
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Step3
The α,β-epoxy ester was
decarboxylated and
hydrolyzed to the aldehyde.
Step4
Reaction with hydroxylamine
gave the oxime
Organic synthesis(cont’d)
• A) The original Boots synthesis of ibuprofen
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Step5
Then convert to the nitrile
Organic synthesis(cont’d)
• A) The original Boots synthesis of ibuprofen
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Organic synthesis(cont’d)
Step6
Finally, hydrolyze to the desired acid(Ibuprofen)
• A) The original Boots synthesis of ibuprofen
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Organic synthesis(cont’d)
• B) The advanced ‘green’ synthesis of ibuprofen
Step1
Friedel-Crafts acetylation
of 2-methylpropylbenzene
Step2
Hydrogenation
with Raney nickel
to give the alcohol
Step3
Finally, underwent
palladium-catalyzed
carbonylation
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Formulation Development
• the dose of ibuprofen
contained in a normal
strength tablet is 200 mg
(0.2 g)
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Formulation Development
Component Function Location
Ibuprofen Active ingredient Core
Croscarmellose sodium Disintegrant Core
Stearic acid Lubricant Core
Sodium laurylsulfate Lubricant Core
Sodium citrate Buffering agent Core
Colloidal anhydrous silica Anticaking agent Core
Carmellose sodium Coating agent Coat
Carnuba wax powder Coating agent Coat
Calcium sulfate dihydrate Diluent Coat
Acacia spray dried Binding agent Coat
Sucrose Binding agent Coat
Titanium dioxide Pigment Coat
Purified water Diluent Coat
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Safety Test
( I )Pre-clinical testing
• Experiment is carried out with cats and
rats.
Findings
• no effect on the cardiovascular system
• did not affect the arterial pressure,
frequency and strength of cardiac
contractions
• not adversely affect respiration
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Safety Test (cont’d)
( I )Pre-clinical testing
• Examinations of the EEG of cats and
rabbits
Findings
• no departures from the normal
whatsoever following administration of
the drug
• no effect on the spasmogenic effects of
acetylcholine, serotonin and bradykinin
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Safety Test (cont’d)
( II ) Human trials
• has undergone extensive clinical trials
Findings:
• possess high therapeutic activity
• improvement in the general condition
• reduction in joint pain, morning
stiffness, swelling of the joints, etc.
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Approval for marketing
• approved by the FDA
in 1974
• approved for sale in
the US and other
states and its
treatment considered
effective
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Approval for marketing
(cont’d)• relieve pains of bones and muscles
• as a painkiller for inflammation
• recommended dose is 600-1200 mg daily
In acute conditions
• increase the daily dose to 1600 mg
**great care in patients suffering from
bronchial asthma
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END