Exam Details
Subject | pharmaceutical analysis ii | |
Paper | ||
Exam / Course | m.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | May, 2017 | |
City, State | gujarat, ahmedabad |
Question Paper
,Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm SEMESTER II- • EXAMINATION SUMMER 2017
Subject Code: 2920107 Date: 29/05/2017
Subject Name: Pharmaceutical Analysis II
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
What is impurity? Give types of impurity. Describe the analytical methods used for analysis of impurities.
08
Describe amino acid sequence analysis and its importance.
08
Q.2
Explain principle, instrumentation and application of LC-MS in study of drug metabolism.
08
Explain exclusion limit. Describe principle, applications and stationary phases used in size exclusion chromatography.
08
Q.3
Describe WHO guidelines for quality control of raw materials used in the herbal formulations.
08
What is Isoelectric Focusing Explain its principle and working. Describe gels used in the IEF.
08
Q.4
Explain flow injection analysis. Discuss theoretical consideration used in FIA.
08
Describe physicochemical evaluation of crude drugs.
08
Q.5
Explain principle and procedure for quantitive analysis of anthistaminics and antihypertensive dosage form.
08
Discuss the principle and role of ion exchange chromatography in amino acid analysis.
08
Q. 6
Discuss the applications of chromatographic techniques used in identification of plant constituents with example.
06
Describe analysis of pesticide residue in plant material.
05
Discuss various impurity threshold as per ICH Q3 guide lines.
05
Q.7
Write a short notes on following
16
Tryptic mapping
Counter current chromatography
Sample preparation techniques
Fluorescence analysis of powder drug
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm SEMESTER II- • EXAMINATION SUMMER 2017
Subject Code: 2920107 Date: 29/05/2017
Subject Name: Pharmaceutical Analysis II
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
What is impurity? Give types of impurity. Describe the analytical methods used for analysis of impurities.
08
Describe amino acid sequence analysis and its importance.
08
Q.2
Explain principle, instrumentation and application of LC-MS in study of drug metabolism.
08
Explain exclusion limit. Describe principle, applications and stationary phases used in size exclusion chromatography.
08
Q.3
Describe WHO guidelines for quality control of raw materials used in the herbal formulations.
08
What is Isoelectric Focusing Explain its principle and working. Describe gels used in the IEF.
08
Q.4
Explain flow injection analysis. Discuss theoretical consideration used in FIA.
08
Describe physicochemical evaluation of crude drugs.
08
Q.5
Explain principle and procedure for quantitive analysis of anthistaminics and antihypertensive dosage form.
08
Discuss the principle and role of ion exchange chromatography in amino acid analysis.
08
Q. 6
Discuss the applications of chromatographic techniques used in identification of plant constituents with example.
06
Describe analysis of pesticide residue in plant material.
05
Discuss various impurity threshold as per ICH Q3 guide lines.
05
Q.7
Write a short notes on following
16
Tryptic mapping
Counter current chromatography
Sample preparation techniques
Fluorescence analysis of powder drug
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