code no. 4140 faculty of pharmacy m. pharmacy …gprcp.ac.in/qpmp/2016/cology 1 all.pdfadrenaline....

15
Library G.Pulla Reddy College of Pharmacy Hyderabad OU - 1705 OU - 1705 Code No. 4140 FACULTY OF PHARMACY M. Pharmacy I-Semester (Common to All) (Main) Examination, March 2017 Subject: Pharmaceutical Analytical Techniques Time: 3 Hours Max. Marks: 75 Note: Answer any five questions. All questions carry equal marks. 1 (a) Explain wood ward fisher rules for calculating absorption maximum for unsaturated hydrocarbons with an example. (7) (b) Write about difference and derivative spectroscopy techniques. (8) 2 (a) Explain in brief about interpretation of IR spectra of organic compounds. (10) (b) Give the absorption frequencies of the following functional groups (5) (i) Ester (ii) Aldehydes (iii) Carboxylic acids (iv) Alcohols (v) Amide 3 (a) Write about different derivation techniques used in gas chromatography. (8) (b) Give the different applications of HPLC techniques. (7) 4 Write short notes on the following: (15) (a) Principle of NMR (b) Chemical shifts in 1 H-NMR (c) Spin-spin coupling in 1 H-NMR 5 (a) Describe the principle and procedure involved in ELISA technique with an example. (8) (b) Give theory and principle involved in electrophoresis technique. (7) 6 (a) What is Nitrogen rule in mass spectrometry? Explain with suitable examples. (5) (b) Make a note on X-Ray crystallography (5) (c) Explain powder diffraction method with its applications (5) 7 (a) Discuss the principles of DTA and DSC techniques. (5) (b) Describe the two techniques used in getting DSC thermograms. (10) 8 Explain about the following : (3x5) (a) Column efficiency parameters (b) Mobile phase selection (c) Column packing materials *****

Upload: vandieu

Post on 26-Apr-2018

214 views

Category:

Documents


0 download

TRANSCRIPT

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 4140FACULTY OF PHARMACY

M. Pharmacy I-Semester (Common to All) (Main) Examination, March 2017

Subject: Pharmaceutical Analytical TechniquesTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Explain wood ward fisher rules for calculating absorption maximum forunsaturated hydrocarbons with an example. (7)

(b) Write about difference and derivative spectroscopy techniques. (8)

2 (a) Explain in brief about interpretation of IR spectra of organic compounds. (10)(b) Give the absorption frequencies of the following functional groups (5)

(i) Ester(ii) Aldehydes(iii) Carboxylic acids(iv)Alcohols(v) Amide

3 (a) Write about different derivation techniques used in gas chromatography. (8)(b) Give the different applications of HPLC techniques. (7)

4 Write short notes on the following: (15)(a) Principle of NMR(b) Chemical shifts in 1H-NMR(c) Spin-spin coupling in 1H-NMR

5 (a) Describe the principle and procedure involved in ELISA technique with anexample. (8)

(b) Give theory and principle involved in electrophoresis technique. (7)

6 (a) What is Nitrogen rule in mass spectrometry? Explain with suitable examples. (5)(b) Make a note on X-Ray crystallography (5)(c) Explain powder diffraction method with its applications (5)

7 (a) Discuss the principles of DTA and DSC techniques. (5)(b) Describe the two techniques used in getting DSC thermograms. (10)

8 Explain about the following : (3x5)(a) Column efficiency parameters(b) Mobile phase selection(c) Column packing materials

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 4153FACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (Main) Examination, March 2017Subject: Principles of Toxicology

Time: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) What are experimental considerations required for assessing possible humanrisks? (8)

(b) Draw a flow chart for development of preclinical toxicity. (7)

2 Explain the new drug safety assessment as per EMEA guidelines. (15)

3 Write a notes on :(a) Mutagenicity testing (8)(b) Allergenicity testing (7)

4 Discuss the following in detail:(a) Lead poisoning (7)(b) Opium poisoning (8)

5 Discuss the risk-benefit assessment and management in pharmacovigilance. (15)

6 Describe the USFDA guidelines for the assessment of new drug safety. (15)

7 Elaborate the in vitro and in vivo toxicity studies for genotoxicity. (15)

8 Write a short note on the following:(a) Serious Adverse Events (SAE) (7)

(b) Suspected unexpected Serious Adverse Reaction (SUSAR) (8)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 4154FACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (Main) Examination, March 2017

Subject: Molecular Pharmacology and Drug DesignTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Write a note on receptor theory. (7)(b) Describe in detail about G-Protein Coupled Receptors. (8)

2 (a) Write a note on protein kinase-A and nitric oxide. (7)(b) Explain in brief about neurosteroids and neuropeptides. (8)

3 (a) Describe in detail about recent advances in angiotensin receptors. (10)(b) Write a note on GABA-A receptor. (5)

4 (a) Describe in detail about Phytochemical screening techniques for herbal extract. (10)(b) Write a note on concept of reverse pharmacognosy. (5)

5 (a) Describe in detail about biochemical based high throughput screeningtechniques. (10)

(b) Write a note on solid phase synthesis. (5)

6 (a) Write a note on third messengers and enzymes linked receptors. (8)(b) Explain in brief about opioid receptors. (7)

7 (a) Describe in detail about herbal anti-diabetics and anti-hyperlipidimics. (10)(b) Write note on regulation of receptors. (5)

8 Write a note on following:(a) Nicotinic receptors (5)(b) Bio-Precursor prodrugs (5)(c) Cytokines (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 4152FACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (Main) Examination, March 2017

Subject: Advanced PharmacologyTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 Explain general principles of chemical transmission. Add a note on cholinergictransmission. (8)

2 What are sympathomimetics ? Classify them. Explain pharmacology ofadrenaline. (1+6+8)

3 Classify antidepressants? Describe the pharmacology of TricyclicAntidepressants. (6+9)

4 Write about the following: (7+8)(a) Pharmacology of purgatives(b) Drug addiction to dependence

5 Classify various types of seizures and drugs used to treat them. (7+8)

6 What are auto coids? Discuss the pharmacology of 5-HT. Add a note on 5HTagonist and antagonist. (1+7+7)

7 Explain biochemical mediators involved in allergy. Write a note oninflammation. (8+7)

8 Discuss the drug treatment for : (8+7)(a) Asthma(b) Emesis

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 4151FACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (Main) Examination, March 2017

Subject: Bioassays and Clinical ResearchTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Define bioassay. Write the principle and advantages of bioassay. (1+2+2)(b) Describe in brief about types of bioassay. (10)

2 (a) Explain the principle and procedure for bioassay of acetylcholine. (7)(b) Describe the bioassay methods for insulin. (8)

3 (a) Write the principle and procedure for bioassay of histamine. (9)(b) Explain any one method for bioassay of serotonin. (6)

4 (a) Describe the principle and bioassay methods for diphtheria vaccine. (9)(b) Write the bioassay method for rota virus vaccine. (6)

5 Explain in detail about phases of clinical trials. (15)

6 (a) Write a note on errors in bioassay. (5)(b) Disadvantages of bioassay. (5)(c) Write a note on applications of bioassay. (5)

7 (a) Write a note on new drug application. (9)(b) Explain about the declaration of helisinki. (6)

8 Write the role and responsibilities of following in clinical research.(a) Sponsorer (5)(b) Investigator (5)(c) Clinical research associate (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

01 O

U - 17

01

Code No. 4097 / NFACULTY OF PHARMACY

M. Pharmacy (Common to All) I-Semester(New) (Suppl.) Examination, October 2016(Except Pharmacognosy / Ind. Pharm.)

Subject: Pharmaceutical Analytical TechniquesTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Explain the following terms with respect to UV-visible spectroscopy. (8)(i) Chromophore (ii) Auxo chrome(iii) Bathochromic shift (iv) Hypsochromic shift

(b) Describe the effect of conjugation and pH on UV absorption of organicmolecules. (7)

2 (a) Write the principle and instrumentation of Fourier Transform Infra Red (FTIR)spectrophotometer with a neat labeled diagram. List out its advantages overconventional IR instrument. (10)

(b) What are ‘IR active and IR inactive groups’? Give the absorption frequencies forthe following functional groups. (3+2)(i) Carboxylic acid (ii) Aldehyde (iii) Primary amine (iv) Alcohol

3 (a) What is spin-spin coupling? Explain with suitable examples. (8)(b) Explain the term ‘chemical shift’? Discuss the factors affecting chemical shift. (7)

4 (a) List out various ionization techniques in mass spectrometry. Explain electronimpact and chemical ionization techniques. (8)

(b) Explain the following:(i) Nitrogen Rule (7)(ii) Molecular ions(iii) Meta stable ion

5 (a) Give the principle of Gas chromatography. Explain any three derivatisationmethods. (9)

(b) Write the applications of Gas chromatography in pharmaceutical analysis. (5)

6 (a) Explain the principle and working of HPLC with a schematic diagram. (8)(b) Discuss the principle and applications of flash chromatography. (7)

7 (a) Write the principle and instrumentation of capillary electrophoresis. (7)(b) Explain the principle, applications and limitations of ELISA. (8)

8 (a) Explain Bragg’s equation and Miller indices. Write the applications ofcrystallographic studies. (8)

(b) Briefly explain the principle and working procedure of TGA. (7)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

01 O

U - 17

01

Code No. 4109 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (New) (Suppl.) Examination, November 2016

Subject: Advanced PharmacologyTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Define Neurotransmitter. Explain various steps involved in neurotransmission. (8)(b) Explain Non-adrenergic and non-cholinergic transmission (NANC). (7)

2 Classify sympathomimetics agents with suitable examples and explain thepharmacology of catecholamines. (15)

3 What are antihypertensives? Classify them with suitable examples. Explain thepharmacology ACE inhibitors. (15)

4 Explain the the following:(a) COX-inhibitors (8)(b) Adverse effects of antibiotics (7)

5 (a) What are anti-anxiety drugs? Explain in detail the pharmacology of benzodia-zepines. (8)

(b) Write a note on anti-diabetic agents. (7)

6 Discuss about cell and biochemicals mediators involved in allergy andinflammation. (15)

7 Write a note on opioid analgesics and drug addiction and dependence. (8+7)

8 (a) Classify antidepressants. Describe the pharmacology of tricyclicanticepressents. (8)

(b) What is arrhythmia? Classify drugs used in cardiac arrhythmias and discussthe pharmacology of Quinidine. (7)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

01 O

U - 17

01

Code No. 4110 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (New) (Suppl.) Examination, November 2016

Subject: Principles of ToxicologyTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) What are experimental considerations required for assessing possible risks? (8)(b) Draw a flow chart for development of preclinical toxicity. (7)

2 Explain the new drug safety assessment as per ICH guidelines. (15)

3 Write note on :(a) Allergenicity testing (8)(b) Ocular toxicity testing (7)

4 Discuss the following in detail :(a) Alcohol poisoning (7)(b) Food poisoning (8)

5 Discuss the different methods for the pharmacovigilance data collection. (15)

6 Describe the USFDA guidelines for the assessment of new drug safety. (15)

7 Elaborate the in vitro and in vivo toxicity studies for mutagenicity. (15)

8 Write short note on the following:(a) Adverse Events (AE) (8)(b) Suspected unexpected serious Adverse Reaction (SUSAR) (7)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

01 O

U - 17

01

Code No. 4111 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (New)(Suppl.) Examination, October 2016

Subject: Molecular Pharmacology and Drug DesignTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Write a note on JAK-STAT pathway. (6)(b) Describe in detail about G-Protein Coupled Receptors. (9)

2 (a) Write a note on neuropeptides. (9)(b) Explain brief about nitric oxide. (6)

3 (a) Describe in brief about endothelin and their modulators. (9)(b) Write a note on histamine receptors. (6)

4 (a) Describe in detail about Phytochemical screening techniques for herbalextract. (10)

(b) Write a note on concept of reverse pharmacognosy. (5)

5 (a) Describe in detail about biochemical based high throughput screeningTechniques. (10)

(b) Write a note on solid phase synthesis. (5)

6 (a) Write a note on third messengers. (6)(b) Explain in brief about opioid receptors. (9)

7 (a) Describe in detail about herbal anti-diabetics and anti-hyperlipidimics. (10)(b) Write a note on regulation of receptors. (5)

8 Write a note on the following:(a) Nicotinic receptors (5)(b) Bio-Precursor prodrugs (5)(c) Cytokines (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

01 O

U - 17

01

Code No. 4108 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester (New)(Suppl.) Examination, November 2016

Subject: Bioassays and Clinical ResearchTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Write the applications of bioassay method. (7)(b) Describe in brief about graded bioassay method. (8)

2 (a) Explain the principle and procedure for bioassay of serotonin. (7)(b) Describe the bioassay methods for histamine. (8)

3 (a) Write the principle and procedure for bioassay of oxytocin. (9)(b) Explain any one method for bioassay of vasopressin. (6)

4 (a) Describe the principle and bioassay method for tetanus antitoxin. (9)(b) Write the bioassay method for rubella vaccine. (6)

5 Explain in detail about phases of clinical trials. (15)

6 (a) Write the composition and responsibilities of IRB. (7)(b) Describe in briefly about clinical trials for special populations. (8)

7 (a) Write a note on informed consent process. (8)(b) Explain about the ethics in clinical trials. (7)

8 Write the role and responsibilities of following in clinical research(a) Coordinator (5)(b) Auditor (5)(c) Contract research organization (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 6097 / NFACULTY OF PHARMACY

M. Pharmacy (Common to All) I-Semester (New) (Main) Examination, April 2016(Except Pharmacognosy / Ind. Pharm.)

Subject: Pharmaceutical Analytical TechniquesTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Explain Woodward – Fieser rules for calculating max for unsaturatedhydrocarbons. (5)

(b) Describe various electronic transitions in UV-visible spectroscopy. (5)(c) List out different IR instruments and discuss their advantages and

Disadvantages. (5)

2 (a) Describe various sample-handling techniques for IR spectroscopy. (8)(b) Write a short note on 13C NMR. (7)

3 (a) How do you determine the molecular formula of a compound with the followingisotopic abundance? (6)

M+ M+1 M+2m/z 94 95 96% R.A. 100 1.1 98

(b) Explain the following with examples. (9)(i) Nitrogen Rule(ii) Shielding and deshielding(iii) Spin-spin coupling

4 (a) Explain the principle of gas chromatography and discuss instrumentation of GCwith a labeled diagram. Give its applications. (9)

(b) Describe the principle and working of any two detectors used in GCinstruments. (6)

5 (a) Explain the principle of HPLC. Describe the stationary phases used in HPLCinstruments. (8)

(b) Discuss the principle and applications of supercritical fluid chromatography. (7)

6 Write a note on :(a) Miller indices and Bragg’s equation (8)(b) SDS-gel electrophoresis (7)

7 (a) Write the principle and instrumentation of zone electrophoresis. (7)(b) Explain the principle, applications and limitations of RIA. (8)

8 (a) List out different thermal analytical techniques. Briefly explain the theory,instrumentation and applications of DSC. (10)

(b) Explain the rotating crystal technique for X-ray diffraction studies. (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 6111 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Year I-Semester(New) (Main) Examination, April 2016

Subject: Molecular Pharmacology and Drug Design

Time: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Write a note on regulation receptors. (7)(b) Describe in detail about Ion channel receptors. (8)

2 (a) Write a note on protein kinase-C and cytokines. (7)(b) Explain in brief about phosphodiesterase enzymes. (8)

3 (a) Describe in detail about types of adrenergic receptors. (10)(b) Write a note on GABA-B receptor. (5)

4 (a) Describe in detail about Phytochemical screening techniques for herbal extract. (10)(b) Write a note on concept of reverse pharmacognosy. (5)

5 (a) Describe in detail about QSAR techniques. (10)(b) Write a note on reporter gene assay. (5)

6 (a) Write a note on second messengers. (8)(b) Explain in brief about Imidazoline receptors. (7)

7 (a) Describe in detail about herbal anti-AIDS and anti-hyperlipidimics. (10)(b) Write a note on nuclear receptors. (5)

8 Write a note on following:(a) Scintillation proximity assays (5)(b) Chemical delivery system (5)(c) Dopamine receptors (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 6108 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Year I-Semester (New) (Main) Examination, April 2016

Subject: Bioassays and Clinical ResearchTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 (a) Describe about the bioassay methods. (8)(b) Write the advantages and disadvantages of bioassay. (7)

2 (a) Explain the principle and procedure for bioassay of heparin. (7)(b) Describe the qualitative bioassay methods for digitals. (8)

3 (a) Write the principle and bioassay methods for oxytocin. (10)(b) Explain any one method for bioassay of adrenaline. (5)

4 (a) Describe about the bioassay for diphtheria anti-toxin. (9)(b) Explain the bioassay method for hepatitis – B Vaccine. (6)

5 Explain in detail about good clinical practice. (15)

6 (a) Explain the bioassay of tetanus vaccine. (10)(b) Write a note on phase-II clinical trial. (5)

7 (a) Write a note on methods of post marketing surveillance. (9)(b) Explain about the NDA. (6)

8 Write the role and responsibilities of following in clinical research.(a) Regulatory authority (5)(b) Auditor (5)(c) Sponsorer (5)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 6110 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester(New) (Main) Examination, April 2016Subject: Principles of Toxicology

Time: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 Write a detailed note on determination of LD50 as per OECD – 425 guideline. (15)

2 Describe the new drug safety assessment as per EMEA guidelines. (15)

3 Write short note on the following:(a) Immunotoxicology testing (8)(b) Dermal toxicity testing (7)

4 Classify poisoning and write general principles of treatment of poisoning. (15)

5 Define pharmacovigilance. Discuss periodic safety update Reports (PSUR) for marketeddrugs. (15)

6 Explain the OECD guidelines for the assessment of new drug safety. (15)

7 Explain various studies for carcinogenicity testing. (15)

8 Discuss the following in detail:(a) Serious Adverse Event (SAE) (7)(b) Serious Adverse Reaction (SAR) (8)

*****

Library

G.Pulla Reddy College of Pharmacy

Hyderabad

OU - 17

05 O

U - 17

05

Code No. 6109 / NFACULTY OF PHARMACY

M. Pharmacy (Pharmacology) I-Semester(New) (Main) Examination, April 2016

Subject: Advanced PharmacologyTime: 3 Hours Max. Marks: 75

Note: Answer any five questions. All questions carry equal marks.

1 Explain general principles of chemical transmission. Add a note on noradrenergictransmission. (15)

2 Classify parasympathamimetics drugs. Write in detail about the pharmacology ofacetylcholine. (15)

3 Explain the following:(a) Depression and mania (8)(b) Drugs acting at NMJ (7)

4 What are autocoids? Discuss the pharmacology of 5HT. Add a note on 5-HT agonistsand antagonists. (1+7+7)

5 Explain the disease pathology and therapeutic agents for allergy and COPD. (15)

6 What are sedatives and hypnotics? Classify them and explain the pharmacology ofphenobarbitone and diazepam. (15)

7 (a) What is congestive heart failure? Discuss various categories of drugs used in itstreatment. (8)

(b) Explain the pharmacology of antifungal agents. (7)

8 Discuss the drug treatment for :(a) Diarrhea (5)(b) Irritable bowel syndrome (5)(c) Emesis (5)

*****