Exam Details
Subject | dosage form design- ii | |
Paper | ||
Exam / Course | b.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | 2018 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
B.PHARM SEMESTER VIII • EXAMINATION WINTER-2017
Subject Code: 2280001 Date: 02/11/2017
Subject Name: Dosage Form Design-II
Time: 02:30 pm to 5:30 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
Discuss the merits and demerits of controlled release formulation
05
What are loading and maintenance dose? How are they calculated?
05
Q.2
Write a note on dissolution and diffusion controlled release system
06
Describe the key components of osmotic drug delivery system with examples.
05
Write a note on colon targeted drug delivery system.
05
Q.3
Discuss the various formulation approaches for floating drug delivery systems.
06
Write about In-vitro-In-vivo evaluations of floating drug delivery systems.
05
Explain pH Sensitive and Prodrug approach to develop colonic Drug Delivery Systems in brief.
05
Q.4
Write in brief about OROS-CT and EOP.
06
Discuss in detail about PULSINCAP Technology.
05
Write a note on: Microspheres.
05
Q.5
Describe formulation and evaluation of transdermal drug delivery system.
06
Define liposomes and niosomes. Describe their evaluation.
05
Write a note on: Hydrogel.
05
Q. 6
What are pharmacokinetic models? Explain in detail one compartment model.
06
Describe the method of residuals for determination of absorption rate constant.
05
Explain Wagner nelson method in detail.
05
Q.7
Explain how one can detect nonlinear pharmacokinetics? Explain Michaelis Menten equation for capacity limited process.
06
Define clinical pharmacokinetics. Explain dosage adjustment in patients with renal failure.
05
Explain term: Drug interaction. Discuss ADME drug interactions with suitable examples.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
B.PHARM SEMESTER VIII • EXAMINATION WINTER-2017
Subject Code: 2280001 Date: 02/11/2017
Subject Name: Dosage Form Design-II
Time: 02:30 pm to 5:30 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
Discuss the merits and demerits of controlled release formulation
05
What are loading and maintenance dose? How are they calculated?
05
Q.2
Write a note on dissolution and diffusion controlled release system
06
Describe the key components of osmotic drug delivery system with examples.
05
Write a note on colon targeted drug delivery system.
05
Q.3
Discuss the various formulation approaches for floating drug delivery systems.
06
Write about In-vitro-In-vivo evaluations of floating drug delivery systems.
05
Explain pH Sensitive and Prodrug approach to develop colonic Drug Delivery Systems in brief.
05
Q.4
Write in brief about OROS-CT and EOP.
06
Discuss in detail about PULSINCAP Technology.
05
Write a note on: Microspheres.
05
Q.5
Describe formulation and evaluation of transdermal drug delivery system.
06
Define liposomes and niosomes. Describe their evaluation.
05
Write a note on: Hydrogel.
05
Q. 6
What are pharmacokinetic models? Explain in detail one compartment model.
06
Describe the method of residuals for determination of absorption rate constant.
05
Explain Wagner nelson method in detail.
05
Q.7
Explain how one can detect nonlinear pharmacokinetics? Explain Michaelis Menten equation for capacity limited process.
06
Define clinical pharmacokinetics. Explain dosage adjustment in patients with renal failure.
05
Explain term: Drug interaction. Discuss ADME drug interactions with suitable examples.
05
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