Exam Details
Subject | dosage form design- ii | |
Paper | ||
Exam / Course | b.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | April, 2016 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm. SEMESTER VIII • EXAMINATION WINTER • 2016
Subject Code: 280001 Date: 18-11-2016
Subject Name: Dosage Form Design II
Time: 02:30 pm 05:30 pm Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Enumerate the factors affecting the designing of oral sustained release drug delivery systems and explain any one in detail.
06
What is the major objective of controlled drug delivery system? Give advantages and disadvantages of such a system
05
Write a note on dissolution and diffusion controlled release system
05
Q.2
Write a note on buccal drug delivery systems.
06
Explain loading dose and maintenance dose used in controlled release formulation
05
Describe the various approaches for colon targeted drug delivery system
05
Q.3
Describe osmotic pressure controlled systems in brief.
06
Discuss the Evaluation methods for Transdermal drug delivery systems.
05
Describe liposomes as a drug delivery system in brief.
05
Q.4
Describe development of ocular controlled drag delivery systems.
06
Describe various methods for preparation of Nanosuspension
05
Give an account of approaches for designing of gastro retentive dosage forms.
05
Q.5
Explain dosage adjustment in patients with renal and hepatic failure.
06
Explain the method of residuals for the calculation of absorption rate constant form oral data.
05
Write a note on: Hydrogel.
05
Q. 6
Give the criteria for obtaining valid urinary excretion method.
06
Explain how one can detect nonlinear pharmacokinetics? Explain Michaelis Menten equation for capacity limited process.
05
Explain the various evaluation parameters for gastro retentive and colon targeted drug delivery system.
05
Q.7
Define "Drug interaction". Explain pharmacokinetic drug interactions giving suitable examples.
06
Define clearance, total body clearance and organ clearance. What is extraction ratio?
05
What are pharmacokinetic models? Explain any one compartment model in details.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm. SEMESTER VIII • EXAMINATION WINTER • 2016
Subject Code: 280001 Date: 18-11-2016
Subject Name: Dosage Form Design II
Time: 02:30 pm 05:30 pm Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Enumerate the factors affecting the designing of oral sustained release drug delivery systems and explain any one in detail.
06
What is the major objective of controlled drug delivery system? Give advantages and disadvantages of such a system
05
Write a note on dissolution and diffusion controlled release system
05
Q.2
Write a note on buccal drug delivery systems.
06
Explain loading dose and maintenance dose used in controlled release formulation
05
Describe the various approaches for colon targeted drug delivery system
05
Q.3
Describe osmotic pressure controlled systems in brief.
06
Discuss the Evaluation methods for Transdermal drug delivery systems.
05
Describe liposomes as a drug delivery system in brief.
05
Q.4
Describe development of ocular controlled drag delivery systems.
06
Describe various methods for preparation of Nanosuspension
05
Give an account of approaches for designing of gastro retentive dosage forms.
05
Q.5
Explain dosage adjustment in patients with renal and hepatic failure.
06
Explain the method of residuals for the calculation of absorption rate constant form oral data.
05
Write a note on: Hydrogel.
05
Q. 6
Give the criteria for obtaining valid urinary excretion method.
06
Explain how one can detect nonlinear pharmacokinetics? Explain Michaelis Menten equation for capacity limited process.
05
Explain the various evaluation parameters for gastro retentive and colon targeted drug delivery system.
05
Q.7
Define "Drug interaction". Explain pharmacokinetic drug interactions giving suitable examples.
06
Define clearance, total body clearance and organ clearance. What is extraction ratio?
05
What are pharmacokinetic models? Explain any one compartment model in details.
05
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- human anatomy physiology and health education-ii
- human anatomy physiology-ii
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- instrumental and process validation
- intellectual property rights and patents
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- pharmaceutical analysis ii
- pharmaceutical analysis iii
- pharmaceutical analysis iv
- pharmaceutical analysis-i
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- pharmaceutical chemistry iii
- pharmaceutical chemistry iv
- pharmaceutical chemistry vii
- pharmaceutical chemistry-i
- pharmaceutical chemistry-i (inorganic chemistry)
- pharmaceutical chemistry-ii (physical chemistry)
- pharmaceutical chemistry-iii (biochemistry – i)
- pharmaceutical chemistry-iv (organic chemistry-i)
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