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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)--- Content provided by FirstRanker.com --- 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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