This document contains questions related to the key concepts in biopharmaceutics and pharmacokinetics across 5 units. The units cover topics like absorption, distribution, metabolism and excretion of drugs; bioavailability and bioequivalence studies; and pharmacokinetic modeling. Some of the main areas addressed include defining absorption and the factors influencing it, distinguishing true from apparent volume of distribution, describing phase I and II drug metabolism reactions, explaining clearance and renal excretion, protocols for bioavailability and bioequivalence studies, and pharmacokinetic parameters and modeling approaches.
This document contains questions related to the key concepts in biopharmaceutics and pharmacokinetics across 5 units. The units cover topics like absorption, distribution, metabolism and excretion of drugs; bioavailability and bioequivalence studies; and pharmacokinetic modeling. Some of the main areas addressed include defining absorption and the factors influencing it, distinguishing true from apparent volume of distribution, describing phase I and II drug metabolism reactions, explaining clearance and renal excretion, protocols for bioavailability and bioequivalence studies, and pharmacokinetic parameters and modeling approaches.
This document contains questions related to the key concepts in biopharmaceutics and pharmacokinetics across 5 units. The units cover topics like absorption, distribution, metabolism and excretion of drugs; bioavailability and bioequivalence studies; and pharmacokinetic modeling. Some of the main areas addressed include defining absorption and the factors influencing it, distinguishing true from apparent volume of distribution, describing phase I and II drug metabolism reactions, explaining clearance and renal excretion, protocols for bioavailability and bioequivalence studies, and pharmacokinetic parameters and modeling approaches.
1) Define absorption. Give a note on passive diffusion
2) Write about formulation factors affecting absorption 3) Give a note on physicochemical factors affecting absorption 4) Write about biological factors affecting absorption 5) Give a note on dissolution theories 6) Give a note on carrier mediated transport 7) Explain about dosage form factors affecting absorption 8) Define biopharmaceutics and pharmacokinetics and explain their role in formulation development 9) What is sink condition? Write about various methods used to maintain sink condition 10) Explain about patient related factors affecting absorption 11) Explain about dosage related factors affecting absorption 12) Discuss about the methods of drug uptake
UNIT-II
1) Enumerate the differences between true and apparent volume of distribution
2) Write about the factors affecting drug distribution 3) Write about the significance of protein binding 4) Explain about kinetics of protein binding with drugs 5) Define and explain the factors influencing protein binding of drugs 6) Explain the mechanisms of drug distribution 7) Explain about BBB 8) Describe the drug protein binding 9) Write about tissue binding of drugs 10) Explain about drug binding to human serum albumin 11) Explain about various physiological barriers for distribution of drugs in body 12) Explain about volume of distribution UNIT-III
1) Describe the metabolism of drugs by phase-I reactions with examples
2) What is meant by enzyme inhibition. Give examples 3) Explain the concept of clearance 4) Explain in brief excretion of drugs through lungs and skin 5) Describe phase-II drug metabolism reactions 6) Explain extraction ratio and the terms involved in it. 7) Write about non renal excretion of drugs 8) Explain enzyme induction. Giving examples 9) Describe the clinical pharmacokinetics in renal and hepatic failures 10) Give a note on principal process of excretion 11) Define clearance and explain about renal clearance 12) Explain about biliary excretion of drugs and entero hepatic cycling of drugs
UNIT-IV
1) Define bioavailabilty. Give the objectives and write a note on measurement of
bioavailability. 2) Explain bioavailability study protocol 3) Explain bioequivalence study protocol 4) Write a note on IVIVC 5) Explain various methods to enhance bioavailability. 6) Explain the methods of assessment of bioavailability from plasma data 7) Explain the methods of assessment of bioavailability from urinary data 8) Describe the terms absolute and relative bioavailability with an equation and write their significance 9) Write about regulatory requirements for conduction of bioequivalence studies 10) Explain statistical interpretation of data. 11) Discuss physicochemical factors influencing bioavailability 12) Discuss biological factors influencing bioavailabilty UNIT-V
1) Give a note on pharmacokinetic parameters
2) Give a note on pharmacodynamic parameters 3) Derive equation for IV bolus drug and explain the pharmacokinetic parameters associated with it. 4) Derive equation for IV infusion and explain the pharmacokinetic parameters associated with it. 5) Derive equation for extravascular administration and explain the pharmacokinetic parameters associated with it. 6) Write a note on urinary excretion studies 7) Give the differences between rate excretion and sigma minus method 8) Explain method of residuals. 9) Determine ka by Wagner Nelson method. 10) Write about non linear pharmacokinetics in detail. 11) Explain non compartmental kinetics 12) Define and explain various pharmacokinetic models.