= ~ [This question paper contains 2 printed pages.] \Se.No.of Question Paper: 1672 Name of the Corse: D. Pharm. ~ Ist year (2015) Name of the Paper Pharmaceutics ~1 Duraton 3 Hours ‘Maximum Marks 80 1, Write your Roll No. on the top immediately on receipt of this question paper. 2. Attempt any five questions. 3, All questions carry equal marks. 4, Different parts of a question should be answered in sequence, 1. Explain the continuous hot extraction for preparation of extract and tinctures. a6) Describe dry heat sterilization and sterilization by filtration. Give the applications of aseptic techniques and sterilization in hospitals. (10+6) 3. (@) Givethe Objectives of size reduetion. With the help of schematic representation explain the working of Ball mill nd give its uses. ao) (6) Discuss the construction and working of Planetary mixer. © 4. Explai ny two ofthe following: (®). Freeze Dryer PTO.1672 (©) Cyclone Separator (©) Evaporating Still and Evaporating Pan (es) ‘5. List different types of compressed tablets, Explain evaluation ftablets. Write an acgount of enterie coating. (34845) 6, What are the advantages and disadvantages of Tablets asa dosage form? Discuss ‘on the step involved inthe production of tablets by wet granulation method. (16) 7. Write notes on any three of the following: @) Filling oFcapsutes (©) Semisoitd dosage forms (©). Pharmacopoeia (@) Toxiods 65.5) (200)[This question paper contains 2 printed pages.] Sr.No. of Question Paper : 1673 ‘Name of the Course: -D, Pharm, ~ Ist Yr. (2015) ‘Name of the Paper I~ Pharmaceutical Chemistry — 1 Duration 3 Hours Maximum Marks 80 Instructions for Candidates 1. Write your Roll No. on the top immediately on receipt of this question paper. 2. Attempt any five questions. 3. All questions carry equal marks. 1. (@)_ What do you understand by limit tests? Discuss the principle, theory and procedure involved in the limit test of chloride and iron. (10) (©) Discuss the principle, theory and procedure involved in the limit test of arsenic. © 2. (@) Define impurities and discuss various sources of impuri in pharmaceutical substances with suitable examples. @) (©) Whatare the signi quality control «) sances of identification test? Discuss different methods of 3. What areradio-pharmaceuticals? Discuss a, (b & ¥ radiations and their biological effects, Write the uses of different radioactive isotopic formulations. a6 4. Writenote on the following (any four) (8) Significant errors PLO.