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AUGUST 2016 Sub. Code: 4267
FOURTH YEAR B.PHARM. EXAMINATION
PAPER I ? FORMULATIVE PHARMACY AND BIOPHARMACEUTICS
Q.P. Code: 564267
Time: Three hours
Maximum: 100 Marks
I. Essay: (2 x 20 = 40)
1. Give an account of stability testing protocol for various pharmaceutical products.
How drug products can be stabilized from the influence of oxidation?
2. Explain about Bio-availability testing.
(8 x 5 = 40)
1. Study of particle size and density of drugs in preformulation studies.
2. Soft gelatin capsule shell and content.
3. Coacervation phase separation.
4. Tablet excipients.
6. Benefits and limitations of prolonged action Pharmaceuticals.
7. Osmotic drug delivery systems.
8. Biological factors influencing gastrointestinal absorption of drugs.
III. Short answers:
(10 x 2 = 20)
1. Significance of drug solubility.
2. Quality control tests on capsules.
4. Sticking and picking in film coated tablets.
5. Difference between prolonged (sustained) release and controlled
release drug delivery systems.
6. Properties of drugs suitable for transdermal drug delivery systems.
7. Raw materials required for liposomes.
8. Apparent volume of distribution.
9. Parameters affecting drug dissolution.
AUGUST 2016 Sub. Code: 4267
--- Content provided by FirstRanker.com ---
FOURTH YEAR B.PHARM. EXAMINATION
PAPER I ? FORMULATIVE PHARMACY AND BIOPHARMACEUTICS
--- Content provided by FirstRanker.com ---
Q.P. Code: 564267
Time: Three hours
--- Content provided by FirstRanker.com ---
--- Content provided by FirstRanker.com ---
Maximum: 100 Marks
I. Essay: (2 x 20 = 40)
--- Content provided by FirstRanker.com ---
1. Give an account of stability testing protocol for various pharmaceutical products.
How drug products can be stabilized from the influence of oxidation?
--- Content provided by FirstRanker.com ---
2. Explain about Bio-availability testing.
--- Content provided by FirstRanker.com ---
II. Short notes:(8 x 5 = 40)
--- Content provided by FirstRanker.com ---
1. Study of particle size and density of drugs in preformulation studies.
2. Soft gelatin capsule shell and content.
3. Coacervation phase separation.
4. Tablet excipients.
--- Content provided by FirstRanker.com ---
5. Formulation of film coating solutions.6. Benefits and limitations of prolonged action Pharmaceuticals.
7. Osmotic drug delivery systems.
8. Biological factors influencing gastrointestinal absorption of drugs.
--- Content provided by FirstRanker.com ---
III. Short answers:
--- Content provided by FirstRanker.com ---
--- Content provided by FirstRanker.com ---
(10 x 2 = 20)
--- Content provided by FirstRanker.com ---
1. Significance of drug solubility.
2. Quality control tests on capsules.
--- Content provided by FirstRanker.com ---
3. Methods of microencapsulate liquids.4. Sticking and picking in film coated tablets.
5. Difference between prolonged (sustained) release and controlled
release drug delivery systems.
--- Content provided by FirstRanker.com ---
6. Properties of drugs suitable for transdermal drug delivery systems.
7. Raw materials required for liposomes.
8. Apparent volume of distribution.
9. Parameters affecting drug dissolution.
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10. Dissolution testing apparatuses.--- Content provided by FirstRanker.com ---
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