Exam Details
Subject | modern analytical techniques | |
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- I • EXAMINATION SUMMER 2017
Subject Code: 910001 Date: 27/04/2017
Subject Name: Modern Analytical Techniques
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 theory and applications of derivative spectroscopy.
06
Give applications of atomic absorption spectroscopy in Pharmacy.
05
Explain principle and working of mass spectroscopy.
05
Q.2
What is reflection spectroscopy? Describe attenuated total reflection spectroscopy with its applications.
06
Describe with diagram, principle and working of Michelson interferometer.
05
What do you mean by X-ray diffraction? Explain Bragg's law and application of X-ray diffraction.
05
Q.3
Give principle of NMR spectroscopy. How NMR spectroscopy helps in the structure elucidation of compounds?
06
Explain the similarities and differences between proton and C13 NMR.
05
Describe Factors affecting the Chemical Shift.
05
Q.4
Enlist the ionization techniques used in mass spectroscopy. Discuss MALDI technique.
06
Describe Mc-Lafferty rearrangement with suitable examples.
05
Write in brief about optical rotatory dispersion and circular dichroism.
05
Q.5
Explain the term capacity factor, tailing factor and resolution.
06
Explain in detail hyphenation technique LC-MS.
05
What is plasma? Describe inductive coupled plasma emission spectroscopy.
05
Q. 6
Explain the terms of Van Demeter equation. Describe eddy and longitudinal diffusion in detail.
06
Explain the principle and instrumentation of Supercritical Fluid chromatography.
05
What is HPLC? Explain the principle of HPLC.
05
Q.7
Enumerate different methods of Thermal analysis. Explain DSC in detail.
06
What are reference standards? Discuss sources, storage and records for reference standards.
05
What is Radio Immuno Assay? Discuss principle and method used in ELISA technique.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm. SEMESTER- I • EXAMINATION SUMMER 2017
Subject Code: 910001 Date: 27/04/2017
Subject Name: Modern Analytical Techniques
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 theory and applications of derivative spectroscopy.
06
Give applications of atomic absorption spectroscopy in Pharmacy.
05
Explain principle and working of mass spectroscopy.
05
Q.2
What is reflection spectroscopy? Describe attenuated total reflection spectroscopy with its applications.
06
Describe with diagram, principle and working of Michelson interferometer.
05
What do you mean by X-ray diffraction? Explain Bragg's law and application of X-ray diffraction.
05
Q.3
Give principle of NMR spectroscopy. How NMR spectroscopy helps in the structure elucidation of compounds?
06
Explain the similarities and differences between proton and C13 NMR.
05
Describe Factors affecting the Chemical Shift.
05
Q.4
Enlist the ionization techniques used in mass spectroscopy. Discuss MALDI technique.
06
Describe Mc-Lafferty rearrangement with suitable examples.
05
Write in brief about optical rotatory dispersion and circular dichroism.
05
Q.5
Explain the term capacity factor, tailing factor and resolution.
06
Explain in detail hyphenation technique LC-MS.
05
What is plasma? Describe inductive coupled plasma emission spectroscopy.
05
Q. 6
Explain the terms of Van Demeter equation. Describe eddy and longitudinal diffusion in detail.
06
Explain the principle and instrumentation of Supercritical Fluid chromatography.
05
What is HPLC? Explain the principle of HPLC.
05
Q.7
Enumerate different methods of Thermal analysis. Explain DSC in detail.
06
What are reference standards? Discuss sources, storage and records for reference standards.
05
What is Radio Immuno Assay? Discuss principle and method used in ELISA technique.
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