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B.Pharm. Eighth Semester
35181 : Pharmaceutics - VI : T-8.1
AW - 2325
Time : Three Hours Max. Marks : 60
Notes:
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- All question carry equal marks.
- Answer any five.
- Illustrate your answer necessary with the help of neat sketches.
- Use of pen Blue/Black ink/refill only for writing the answer book.
- Discuss in detail various approaches used to prepare parenteral controlled release drug delivery system & add a note on its evaluation. (12)
- i) Discuss in detail the need & importance of stabilization of pharmaceutical product. (6)
ii) Explain in detail stability testing protocol for liquid oral & semisolid dosage form. (6) - Discuss in detail about preparation of microcapsules by coacervation phase separation method & multi orifice centrifugation methods. (12)
- Define & classify validation method. Explain in detail process validation involved in production of tablets. (12)
- i) Explain in detail various types of transdermal drug delivery systems. (6)
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ii) Define & classify liposomes. Enlist various methods to prepare liposome & describe ethanol injection method in detail. (6) - a) Explain in detail about resealed erythrocytes & add a note on limitation of it. (6)
b) Add a note on "Evaluation of microcapsules". (6) - Write notes on any two. (12)
a) Applications of polymers in pharmaceutical formulations.--- Content provided by FirstRanker.com ---
b) Retrospective validation
c) Nano Spheres
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AW -2325
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