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AKTU Pharmaceutical Dosage Forms II (Practical) (BP509P) Syllabus PDF – B.Pharm 5th Semester
Pharmaceutical Dosage Forms II (Practical) BP509P
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Official AKTU syllabus of Pharmaceutical Dosage Forms II (Practical) (BP509P) for B.Pharm 5th 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 — Pharmaceutical Dosage Forms II (Practical)
Download PDFBP509P · 1 credits · L-T-P 0-0-3
Course Objectives
- Understand various solubility enhancement techniques.
- Provide hands-on experience in manufacturing processes and evaluation of monophasic and biphasic liquid dosage forms.
- Provide hands-on experience in manufacturing processes and evaluation of semisolid dosage forms.
- Learn manufacturing processes and evaluation of pressurised dosage forms.
- Understand the effects of formulation parameters on the performance of biphasic and semisolid dosage forms.
Course Outcomes
| CO | Upon successful completion of this course, the students will be able to: |
| No. | |
| 1 | Apply the fundamentals of solubility enhancement during dosage form development. |
| 2 | Explain manufacturing processes of monophasic and biphasic liquid dosage forms. |
| 3 | Demonstrate manufacturing processes of semisolid dosage forms. |
| 4 | Provide insights into evaluation of dosage forms. |
| 5 | Compare the effects of formulation parameters on the performance of biphasic and semisolid dosage forms. |
Course Content
List of Experiments
(Minimum 12 experiments must be performed)
- To enhance the solubility of a BCS Class II drug by solid dispersion technique.
- To enhance the solubility of a BCS Class II drug by cyclodextrin complexation.
- Preparation and evaluation of medicated syrups using simple and artificial syrup bases.
- Preparation and evaluation of different types of pharmaceutical emulsions.
- Preparation and evaluation of an emulsion with a small-dose oily active (e.g., calciferol).
- Preparation and evaluation of an oral suspension.
- To study the effect of different suspending agents/concentrations on sedimentation volume.
- Preparation and evaluation of a dry powder for reconstitution as a suspension.
- Preparation and evaluation of pharmaceutical creams.
- Preparation and evaluation of pharmaceutical gels.
- To study the effect of different gelling agents/concentrations on viscosity of gels.
- Preparation and evaluation of medicated suppositories.
- Preparation and evaluation of medicated pessaries.
- Preparation and evaluation of in-situ gels.
- Preparation and evaluation of emulgels.
Recommended References
- Aulton, M. E. Elsevier.
- Gibson, M. Pharmaceutical Preformulation and Formulation. CRC Press.
- Lachman, L., Lieberman, H. A. and Kanig, J. L. The Theory and Practice of Industrial Pharmacy. CBS Publishers & Distributors.
- Robinson, J. R. and Lee, V. H. L. Controlled Drug Delivery: Fundamentals and Applications. CRC Press.
- Troy, D. B. and Beringer, P. Remington: The Science and Practice of Pharmacy. Pharmaceutical Press.
- Indian Pharmacopoeia. Indian Pharmacopoeia Commission.
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