Exam Details
Subject | advances in drug delivery system | |
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: MPT102T Date: 03/01/2019
Subject Name: Advances in drug delivery system
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
Discuss basic concepts of sustained and controlled drug delivery systems.
06
Give classification of oral controlled drug delivery systems.
05
Discus mechanism of drug delivery from SR/CR formulation.
05
Q.2
Discuss the suitable excipients for osmotic drug delivery system. Which API's can be formulated by this approach? Why?
06
Describe physic-chemical and biological factors influencing dissolution and diffusion controlled systems.
05
Describe criteria for the drug candidate selection for SR/CR dosage forms.
05
Q.3
List out the factors affecting the designing of oral sustained release drug delivery system and discuss any one in detail to formulate it.
06
Write a note on mucoadhesive drug delivery system.
05
Define microencapsulation. Mention objectives of microencapsulation.
05
Q.4
Enlist various approaches for the preparation of microcapsules. Explain any two.
06
Describe various evaluations of microcapsules.
05
Write a note on intra muscular implants.
05
Q.5
Define Implants and Inserts. Discuss the applications, techniques and mechanism of drug release for subcutaneous implants with examples.
06
Write a note on Intra vaginal Inserts.
05
Write a note on sonophoresis.
05
Q. 6
What are the approaches for formulation development of transdermal drug delivery systems? Explain in details.
06
Discuss physicochemical biological approaches for sustained release formulations.
05
Discuss percutaneous absorption through skin.
05
Q.7
Discuss 3D printing of pharmaceuticals and telepharmacy.
06
Describe various evaluation parameters of Transdermal drug delivery systems.
05
Write a note on personalized medicine.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: MPT102T Date: 03/01/2019
Subject Name: Advances in drug delivery system
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
Discuss basic concepts of sustained and controlled drug delivery systems.
06
Give classification of oral controlled drug delivery systems.
05
Discus mechanism of drug delivery from SR/CR formulation.
05
Q.2
Discuss the suitable excipients for osmotic drug delivery system. Which API's can be formulated by this approach? Why?
06
Describe physic-chemical and biological factors influencing dissolution and diffusion controlled systems.
05
Describe criteria for the drug candidate selection for SR/CR dosage forms.
05
Q.3
List out the factors affecting the designing of oral sustained release drug delivery system and discuss any one in detail to formulate it.
06
Write a note on mucoadhesive drug delivery system.
05
Define microencapsulation. Mention objectives of microencapsulation.
05
Q.4
Enlist various approaches for the preparation of microcapsules. Explain any two.
06
Describe various evaluations of microcapsules.
05
Write a note on intra muscular implants.
05
Q.5
Define Implants and Inserts. Discuss the applications, techniques and mechanism of drug release for subcutaneous implants with examples.
06
Write a note on Intra vaginal Inserts.
05
Write a note on sonophoresis.
05
Q. 6
What are the approaches for formulation development of transdermal drug delivery systems? Explain in details.
06
Discuss physicochemical biological approaches for sustained release formulations.
05
Discuss percutaneous absorption through skin.
05
Q.7
Discuss 3D printing of pharmaceuticals and telepharmacy.
06
Describe various evaluation parameters of Transdermal drug delivery systems.
05
Write a note on personalized medicine.
05
Other Question Papers
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