Biopharmaceutics and Pharmacokinetics Question paper

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MOST IMPORTANT QUESTIONS of Biopharmaceutics and Pharmacokinetics (B.pharm 6th semester), Here are a Selective questions of previous years questions papers collected by the different sources. this question papers are very helpful to all B. pharm 6th Sem students.

Question -02 marks

  • Write the name the various barriers for drugs distribution.
  • Define apparent volume of distribution and protein binding of drug.
  • Define renal clearance. Give the name of non-renal routs of drug excretion of drugs.
  • What is the advantage of IV infusion injection.
  • Define bio-availability and bio-equivalence.
  • Classify different types of pharmacokinetics models.
  • Enumerate the factors affecting drug distribution.
  • Write the difference between absolute with relative bioavailability.
  • Give the advantage of physiological models.
  • Define nonlinear pharmacokinetics.
  • Define total clearance.
  • What is the significance of maintain steady state drug levels in pharmacokinetics?.
  • Give Michaelis equation.

Question -10 marks

  • Enlist various factors influencing GI absorption of a drug from its dosage form and explain physicochemical factors affecting drug absorption in detail.
  • Discuss in detail two-compartment open model for a drug administration as IV bolus. Give the schematic representation, graphs and equation for the same.
  • Discuss the various mechanism of drug absorption through GIT.
  • How will you calculate loading dose? Discuss its role in maintains of dose.
  • Describe Michaelis mention methods of estimation pharmacokinetic parameters.
  • What is the difference between linear and non- linear pharmacokinetics? List out the reasons for non-linearity in pharmacokinetics studies.

Question -07 marks

  • Discuss in detail the various pharmaceutical factors affecting drug absorption.
  • Explain the following terms- Clearance, Total body clearance, Hepatic clearance and renal clearance.
  • Explain in detail the plasma level time curve for a two compartment open model.
  • What do you mean by drug metabolism? Explain factors affecting renal excretion of drugs.
  • Enumerate the objective of bioavailability. Discuss the direct methods for its assessment.
  • Give the kinetics of protein binding along with its clinical significance
  • What is AUC? Describe the trapezoidal methods for its calculation.
  • Describe the method to calculate absorption rate constant for one compartment open model extra vascular first order kinetics.
  • What is the reason behind initial rapid decline and terminal slow decline of the conc. of drug in the central compartment? Discuss the reason.
  • How will you affect dosage adjustment in renal failure?
  • Describe the various methods aimed at enhancing bioavailability of drug from its dosage form.
  • Describe the kinetics of capacity limited or suitable processes of non linearity.

By Dr. Avinash Joriya

Dr. Avinash Joriya is the Founder & CEO of Edupharmaexpert.in and an Associate Professor with over 7 years of expertise in pharmacy education and pharmacological research. A B.Pharm and M.Pharm alumnus of AKTU Lucknow, he has contributed to major government projects like Namami Gange (NMCG). With 5 published textbooks and an Indian Design Patent, Dr. Joriya is dedicated to mentoring students and bridging the gap in the pharma profession. We provide specialized guidance on Pharmacy careers (D.Pharm to PhD), alongside expert takes on Health, Education, Travel, Technology, Finance, and Books, helping the next generation of professionals build better habits and successful careers. And Never miss any New updates from Edupharmaexpert.in

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