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AKTU Biopharmaceutics and Pharmacokinetics (Practical) (BP608P) Syllabus PDF – B.Pharm 6th Semester
Biopharmaceutics and Pharmacokinetics (Practical) BP608P
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Official AKTU syllabus of Biopharmaceutics and Pharmacokinetics (Practical) (BP608P) for B.Pharm 6th Semester – 1 credits, L-T-P 0-0-3. Read the unit-wise course content, course outcomes, evaluation pattern and recommended books online, or download the PDF.
Syllabus — Biopharmaceutics and Pharmacokinetics (Practical)
Download PDFBP608P · 1 credits · L-T-P 0-0-3
Course Objectives
- 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
| CO | Upon successful completion of this course, the students will be able to: |
| No. | |
| 1 | Explain the fundamental concepts, types, and applications of NDDS in modern therapeutics and precision medicine. |
| 2 | Design 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 | Select appropriate excipients and techniques for the development of NDDS considering drug properties, patient needs, and target site requirements. |
| 4 | Perform evaluation and quality control tests for novel formulations to ensure efficacy, stability, and patient compliance. |
| 5 | Integrate NDDS strategies into precision medicine frameworks to optimize dosing, therapeutic targeting, and individualized treatment plans. |
Course Content
List of Practical
- To calculate MRT from the given data.
- To assess the effect of protein binding of a drug
- To report relative bioavailability of given drug product using urinary excretion data
- To report relative bioavailability of given drug product using plasma data
- Establish IVIVC from the given in vitro and in vivo data.
- To calculate pharmacokinetic parameters of a drug using given plasma level data.
- To report bioequivalence of drug products using given urinary excretion data administered
- To calculate absorption rate constant, elimination rate constant and elimination half-life of given excretion data by sigma minus method.
- To 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.
- To calculate the absorption rate constant by using curve fitting method.
- To calculate various pharmacokinetic parameters using in silico methods.
Recommended References
- Bonate, P. L. Pharmacokinetic-Pharmacodynamic Modeling and Simulation. Springer.
- Brahmankar, D. M. and Jaiswal, S. B. Biopharmaceutics and Pharmacokinetics: A Treatise. Vallabh Prakashan.
- Eddy, D. M. Modeling and Simulation in the Medical and Health Sciences. Springer.
- Gibaldi, M. Biopharmaceutics and Clinical Pharmacokinetics. Lea & Febiger.
- Rowland, M. and Tozer, T. N. Clinical Pharmacokinetics and Pharmacodynamics. Wolters Kluwer.
- Shargel, L. and Yu, A. B. C. Applied Biopharmaceutics and Pharmacokinetics. McGraw- Hill Education.
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