Exam Details
Subject | pharmaceutical analysis ii | |
Paper | ||
Exam / Course | m.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | December, 2018 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
B.Pharm. SEMESTER- II • EXAMINATION WINTER -2018
Subject Code: 2220003 Date: 11/12/2018
Subject Name: Pharmaceutical Analysis-II
Time: 02:30 PM TO 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
Explain the principle, application and types of paper chromatography.
06
Write a short note on Thin Layer chromatography.
05
Briefly explain Retention mechanisms involved in chromatography.
05
Q.2
Comment on the following statements:
Potassium chloride is preferred in salt bridge.
ii) Conductance of HCl in non-polar solvent is higher than conductance of HCl in polar solvent.
iii) Separation efficiency is independent of number of plates.
06
Write a detailed note on Conductometric titrations.
05
Describe factor affecting conductance.
05
Q.3
What is emf. Classify electrode and what are the ideal characteristics of indicator electrode.
06
Discuss the applications of potentiometry.
05
Define Reference electrode. Enlist the types of it and write note on standard calomel.
05
Q.4
Describe principle, working and applications of Polarimetry.
06
Write a short note on Biamperometric titration.
05
Give difference between optically active and optically inactive compound.
05
Q.5
Describe instrumentation of TGA.
06
Discuss the advantages, disadvantages and limitation of instrumental method of analysis.
05
Explain the application of DSC in detail.
05
Q. 6
Define validation. Enlist parameters of analytical method validation and explain the source of noise in instrumental analysis.
06
Describe multiple extraction technique. How pH affect extractability of the drugs.
05
Discuss the theory of extraction.
05
Q.7
Write note on NPP and DPP.
06
What is stripping voltammetry? Explain in detail any two techniques.
05
Describe the oxygen combustion flask method.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
B.Pharm. SEMESTER- II • EXAMINATION WINTER -2018
Subject Code: 2220003 Date: 11/12/2018
Subject Name: Pharmaceutical Analysis-II
Time: 02:30 PM TO 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
Explain the principle, application and types of paper chromatography.
06
Write a short note on Thin Layer chromatography.
05
Briefly explain Retention mechanisms involved in chromatography.
05
Q.2
Comment on the following statements:
Potassium chloride is preferred in salt bridge.
ii) Conductance of HCl in non-polar solvent is higher than conductance of HCl in polar solvent.
iii) Separation efficiency is independent of number of plates.
06
Write a detailed note on Conductometric titrations.
05
Describe factor affecting conductance.
05
Q.3
What is emf. Classify electrode and what are the ideal characteristics of indicator electrode.
06
Discuss the applications of potentiometry.
05
Define Reference electrode. Enlist the types of it and write note on standard calomel.
05
Q.4
Describe principle, working and applications of Polarimetry.
06
Write a short note on Biamperometric titration.
05
Give difference between optically active and optically inactive compound.
05
Q.5
Describe instrumentation of TGA.
06
Discuss the advantages, disadvantages and limitation of instrumental method of analysis.
05
Explain the application of DSC in detail.
05
Q. 6
Define validation. Enlist parameters of analytical method validation and explain the source of noise in instrumental analysis.
06
Describe multiple extraction technique. How pH affect extractability of the drugs.
05
Discuss the theory of extraction.
05
Q.7
Write note on NPP and DPP.
06
What is stripping voltammetry? Explain in detail any two techniques.
05
Describe the oxygen combustion flask method.
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