BP608P

Biopharmaceutics and Pharmacokinetics (Practical)

L-T-P0-0-3 Credits1 Session2026-27 TypeLab / Practical
Appears in 1 semester

B.Pharm · Sem 6 (Lab)

List of Experiments / Activities

  1. Biopharmaceutics and Pharmacokinetics (Practical) Core Credit Hours Per Week (L-T-P) Max. Hours. L T P
  2. 1-- --
  3. 45Maximum Marks SE ESE
  4. 1To calculate MRT from the given data.
  5. 2To assess the effect of protein binding of a drug
  6. 3To report relative bioavailability of given drug product using urinary excretion data
  7. 4To report relative bioavailability of given drug product using plasma data
  8. 5Establish IVIVC from the given in vitro and in vivo data.
  9. 6To calculate pharmacokinetic parameters of a drug using given plasma level data.
  10. 7To report bioequivalence of drug products using given urinary excretion data administered
  11. 8To calculate absorption rate constant, elimination rate constant and elimination half-life of given excretion data by sigma minus method.
  12. 9To calculate absorption rate constant, elimination rate constant and elimination half-life of the given drug data administered by IV bolus injection represented by one compartment model.
  13. 10To calculate the absorption rate constant by using curve fitting method.
  14. 11To calculate various pharmacokinetic parameters using in silico methods.
Course Objectives6 points
  • The objectives of this course are to:
  • Understand the dissolution profiles of pharmaceutical formulations using various media and conditions.
  • Apply in vitro and ex vivo techniques to assess drug absorption, dissolution, and bioavailability.
  • Interpret pharmacokinetic parameters using plasma and urinary excretion data.
  • Establish in vitro in vivo correlation (IVIVC) for drug products based on experimental datasets.
  • Utilize software tools to simulate and analyze pharmacokinetic and pharmacodynamic data.
Course Outcomes (COs)5 outcomes

After completion of the course student will be able to:

  1. CO1Explain the fundamental concepts, types, and applications of NDDS in modern therapeutics and precision medicine.
  2. CO2Design and prepare advanced drug delivery systems such as orodispersible tablets, bilayer tablets, osmotic systems, microspheres, microcapsules, buccal/sublingual dosage forms, transdermal patches, gastroretentive systems, and lipid-based carriers.
  3. CO3Select appropriate excipients and techniques for the development of NDDS considering drug properties, patient needs, and target site requirements.
  4. CO4Perform evaluation and quality control tests for novel formulations to ensure efficacy, stability, and patient compliance.
  5. CO5Integrate NDDS strategies into precision medicine frameworks to optimize dosing, therapeutic targeting, and individualized treatment plans.
Recommended References (Preferably latest editions):6 books
  1. Bonate, P. L. Pharmacokinetic-Pharmacodynamic Modeling and Simulation. Springer.
  2. Brahmankar, D. M. and Jaiswal, S. B. Biopharmaceutics and Pharmacokinetics: A Treatise. Vallabh Prakashan.
  3. Eddy, D. M. Modeling and Simulation in the Medical and Health Sciences. Springer.
  4. Gibaldi, M. Biopharmaceutics and Clinical Pharmacokinetics. Lea & Febiger.
  5. Rowland, M. and Tozer, T. N. Clinical Pharmacokinetics and Pharmacodynamics. Wolters Kluwer.
  6. Shargel, L. and Yu, A. B. C. Applied Biopharmaceutics and Pharmacokinetics. McGraw- Hill Education. Course Title Course Type

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Official AKTU syllabus

This subject is on page 168, 169, 170 of the original AKTU PDF.

Official AKTU syllabus PDF ↗