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Roll No. __________________ Total No. of Pages : 01
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Total No. of Questions : 06
M.Pharmacy (Pharmaceutics) (2017 Batch) (Sem.-2)
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS
Subject Code : MPH-202
M.Code : 74962 Max. Marks: 75
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Time: 3 Hrs.
INSTRUCTIONS TO CANDIDATES :
- Attempt any FIVE questions out of SIX questions.
- Each question carries FIFTEEN marks.
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- Discuss the physico-chemical factors influencing drug dissolution from dosage forms. (7.5)
- Give an account of Tight Junction Complex and its role in drug transport through the intestine. (7.5)
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- Explain pH-partition hypothesis for predicting drug absorption. (7.5)
- Give an account of IVIVC methods and their utility. (7.5)
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- Distinguish one compartment from two compartment model. Derive a simple equation for predicting the plasma drug concentration for one compartment open model after IV bolus injection. (7.5)
- Write a note on CyP 450 based interactions. (7.5)
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- What are biosimilars? Briefly explain biosimilars and their general compendial requirements. (7.5)
- Give an account of the study designs used for bioequivalence assessment of drug products. (7.5)
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- What is non-linear pharmacokinetics? Mention the reasons for this behavior with suitable examples. (7.5)
- Discuss briefly the methods used for assessing permeability of drug molecules in vitro. (7.5)
- Write short notes on :
- Generic substitution with examples (5)
- Pharmacokinetics of peptides (5)
- Immunotherapy and its modules (5)
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NOTE: Disclosure of Identity by writing Mobile No. or Making of passing request on any page of Answer Sheet will lead to UMC against the Student.
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This download link is referred from the post: PTU M.Pharm 2020 March Previous Question Papers
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