Exam Details
| Subject | pharmaceutical formulation and development | |
| Paper | ||
| Exam / Course | m.pharm | |
| Department | ||
| Organization | Gujarat Technological University | |
| Position | ||
| Exam Date | January, 2019 | |
| City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MPT103T Date: 05/01/2019
Subject Name: Pharmaceutical formulation and development
Time :10:30 AM TO 01:30 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
Explain significance of drug excipients incompatibility in preformulation study.
06
What is preformulation study? Discuss the significance of particle size and shape in formulation.
05
Write a note on hygroscopicity and crystallanity.
05
Q.2
Write a short note on DSC.
06
Discuss importance of FTIR in preformulation study
05
Write a short note on X-Ray diffraction.
05
Q.3
How dissolution data are compared? Describe dissolution profile comparison based on f1 and f2.
06
Discuss importance and objectives of Dissolution studies.
05
Write a short note on BCS classification.
05
Q.4
Enlist techniques used for solubility improvement. Discuss solid dispersion in detail.
06
Define Solubility. Describe factors affecting on solubility.
05
Discuss about selection of dissolution media and conditions
05
Q.5
Write a short note on basic concepts and objectives of stability study
06
Write a short note on accelerated stability study
05
Discuss mechanisms of solubilization.
05
Q. 6
Discuss various factors affecting on stability of Pharmaceutical formulations
06
Discuss regulatory requirements for climate zone in stability study.
05
Write a note on applications of biomaterials in pharmaceutical formulations.
05
Q.7
Write a short note on cylcodextrins.
06
Discuss factors affecting for the selection of excipients in pharmaceutical formulations.
05
Write a short note on film coating polymers
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MPT103T Date: 05/01/2019
Subject Name: Pharmaceutical formulation and development
Time :10:30 AM TO 01:30 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
Explain significance of drug excipients incompatibility in preformulation study.
06
What is preformulation study? Discuss the significance of particle size and shape in formulation.
05
Write a note on hygroscopicity and crystallanity.
05
Q.2
Write a short note on DSC.
06
Discuss importance of FTIR in preformulation study
05
Write a short note on X-Ray diffraction.
05
Q.3
How dissolution data are compared? Describe dissolution profile comparison based on f1 and f2.
06
Discuss importance and objectives of Dissolution studies.
05
Write a short note on BCS classification.
05
Q.4
Enlist techniques used for solubility improvement. Discuss solid dispersion in detail.
06
Define Solubility. Describe factors affecting on solubility.
05
Discuss about selection of dissolution media and conditions
05
Q.5
Write a short note on basic concepts and objectives of stability study
06
Write a short note on accelerated stability study
05
Discuss mechanisms of solubilization.
05
Q. 6
Discuss various factors affecting on stability of Pharmaceutical formulations
06
Discuss regulatory requirements for climate zone in stability study.
05
Write a note on applications of biomaterials in pharmaceutical formulations.
05
Q.7
Write a short note on cylcodextrins.
06
Discuss factors affecting for the selection of excipients in pharmaceutical formulations.
05
Write a short note on film coating polymers
05
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Subjects
- advanced medicinal chemistry
- advanced organic chemistry-i
- advanced organic chemistry-ii
- advanced pharmacology ii
- advanced pharmacology-i
- advances in drug delivery system
- advances in pharmacology
- applied pharmacotherapeutics - ii
- applied pharmacotherapeutics-i
- audits and regulatory compliance
- biological evaluations & clinical research
- cellular and molecular pharmacology
- clinical and hospital pharmacy
- clinical pharmacy practice
- clinical research and pharmacy practice
- clinical research and regulatory affairs
- clinical research regulations
- cosmetic and cosmeceuticals
- documentation and regulatory writing
- drug design and discovery
- drug regulation and regulatory authority
- experimental design and patents
- global regulatory requirements
- gmp, glp and validation
- good manufacturing and good laboratory practice
- good manufacturing practice and process validation
- good regulatory practices
- hazards and safety management
- industrial pharmacy practice
- modern analytical techniques
- modern pharmaceutical analysis
- novel drug delivery system part-i
- novel drug delivery system-ii
- pharm. management -ii
- pharmaceutical analysis ii
- pharmaceutical and cosmetic analysis
- pharmaceutical formulation and development
- pharmaceutical formulation development and biopharmceutics
- pharmaceutical manufacturing technology
- pharmaceutical production management & technology
- pharmaceutical regulatory affairs
- pharmacological and toxicological screening methods-i
- pharmacological and toxicological screening methods-ii
- pharmacometrics and methods of biological evaluation of drugs
- pharmacotherapeutics
- principles of biopharmaceutics& pharmacokinetics
- product development and technology transfer
- quality control & quality assurance
- quality control and quality assurance
- quality management system
- regulatory affairs - i
- regulatory affairs and new drug applications
- regulatory aspects of hebbal and biologicals
- research methodology
- validation and product development