GTU B.Pharma 2018 Summer Question Papers || Gujarat Technological University
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Seat No.:
Subject Code: 2270002
GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm. - SEMESTER-7 * EXAMINATION - SUMMER -2018
Subject Name: Pharmaceutical Technology I
Time: 02:30 PM TO 05:30 PM
Date: 22/05/2018
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
Q.1 (a) Give classification of Liquid dosage form. Enumerate formulation components with its use. 06
(b) Write a note on “Solubility Enhancers” and “Vehicles”. 05
(c) Enumerate evaluation parameters of suspensions and discuss the procedures. 05
Q.2 (a) Discuss 1) Micro-Emulsions & ii) Multiple Emulsions. 06
(b) Explain the mechanism of drug penetration through skin. Write a short note on permeation enhancers. 05
(c) Discuss in brief suppository bases & classify them. 05
(b) Role and properties of propellants. Discuss. 05
(c) How will you evaluate aerosols? 05
Q.4 (a) Define “Sterile Dosage forms” classify-them. What are the ideal requirements for it? 06
(c) Describe freeze dried products: its production & application. 05
Q.5 (a) Sterility is maintained strictly in blow fill & seal technology : comment 06
(b) “Water for Injection”Preparation & quality control. 05
Q.6 (a) Requirement and purpose of sun-screen lotions. Categories & Classification. 06
(b) Enlist products covered under cosmeceuticals. Explain shampoo in details. 05
(c) What do-you understand by validation? 05
Q.7 (a) Briefly outline schedule-M. 06
(b) What is the importance of Documentation in GMP? 05
(c) Write a note on “Recovery & Reprocessing.” 05
Seat No.:
Subject Code: 2270002
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Enrolment No.GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm. - SEMESTER-7 * EXAMINATION - SUMMER -2018
Subject Name: Pharmaceutical Technology I
Time: 02:30 PM TO 05:30 PM
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Total Marks: 80Date: 22/05/2018
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
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3. Figures to the right indicate full marks.Q.1 (a) Give classification of Liquid dosage form. Enumerate formulation components with its use. 06
(b) Write a note on “Solubility Enhancers” and “Vehicles”. 05
(c) Enumerate evaluation parameters of suspensions and discuss the procedures. 05
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Q.2 (a) Discuss 1) Micro-Emulsions & ii) Multiple Emulsions. 06
(b) Explain the mechanism of drug penetration through skin. Write a short note on permeation enhancers. 05
(c) Discuss in brief suppository bases & classify them. 05
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Q.3 (a) Draw well labeled diagram for aerosol packs. Explain the different parts of it. 06(b) Role and properties of propellants. Discuss. 05
(c) How will you evaluate aerosols? 05
Q.4 (a) Define “Sterile Dosage forms” classify-them. What are the ideal requirements for it? 06
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(b) Outline the design and requirements for production area of sterile products. 05(c) Describe freeze dried products: its production & application. 05
Q.5 (a) Sterility is maintained strictly in blow fill & seal technology : comment 06
(b) “Water for Injection”Preparation & quality control. 05
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(c) Short note on “Pre-filled syringes” 05Q.6 (a) Requirement and purpose of sun-screen lotions. Categories & Classification. 06
(b) Enlist products covered under cosmeceuticals. Explain shampoo in details. 05
(c) What do-you understand by validation? 05
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Q.7 (a) Briefly outline schedule-M. 06
(b) What is the importance of Documentation in GMP? 05
(c) Write a note on “Recovery & Reprocessing.” 05
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