UNIQUE SERIES AKTU Syllabus
BP509P

Pharmaceutical Dosage Forms II (Practical)

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

B.Pharm · Sem 5 (Lab)

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List of Experiments / Activities

  1. Pharmaceutical Dosage Forms II (Practical) Core Credit Hours Per Week (L-T-P) Max. Hours. L T P
  2. 1-- --
  3. 45Maximum Marks SE ESE
  4. (Minimum 12 experiments must be performed)
  5. 1To enhance the solubility of a BCS Class II drug by solid dispersion technique.
  6. 2To enhance the solubility of a BCS Class II drug by cyclodextrin complexation.
  7. 3Preparation and evaluation of medicated syrups using simple and artificial syrup bases.
  8. 4Preparation and evaluation of different types of pharmaceutical emulsions.
  9. 5Preparation and evaluation of an emulsion with a small-dose oily active (e.g., calciferol).
  10. 6Preparation and evaluation of an oral suspension.
  11. 7To study the effect of different suspending agents/concentrations on sedimentation volume.
  12. 8Preparation and evaluation of a dry powder for reconstitution as a suspension.
  13. 9Preparation and evaluation of pharmaceutical creams.
  14. 10Preparation and evaluation of pharmaceutical gels.
  15. 11To study the effect of different gelling agents/concentrations on viscosity of gels.
  16. 12Preparation and evaluation of medicated suppositories.
  17. 13Preparation and evaluation of medicated pessaries.
  18. 14Preparation and evaluation of in-situ gels.
  19. 15Preparation and evaluation of emulgels.
Course Objectives6 points
  • The objectives of this course are to:
  • 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 (COs)5 outcomes

After completion of the course student will be able to:

  1. CO1Apply the fundamentals of solubility enhancement during dosage form development.
  2. CO2Explain manufacturing processes of monophasic and biphasic liquid dosage forms.
  3. CO3Demonstrate manufacturing processes of semisolid dosage forms.
  4. CO4Provide insights into evaluation of dosage forms.
  5. CO5Compare the effects of formulation parameters on the performance of biphasic and semisolid dosage forms.
Recommended References (Preferably latest editions):6 books
  1. Aulton, M. E. Elsevier.
  2. Gibson, M. Pharmaceutical Preformulation and Formulation. CRC Press.
  3. Lachman, L., Lieberman, H. A. and Kanig, J. L. The Theory and Practice of Industrial Pharmacy. CBS Publishers & Distributors.
  4. Robinson, J. R. and Lee, V. H. L. Controlled Drug Delivery: Fundamentals and Applications. CRC Press.
  5. Troy, D. B. and Beringer, P. Remington: The Science and Practice of Pharmacy. Pharmaceutical Press.
  6. Indian Pharmacopoeia. Indian Pharmacopoeia Commission. Course Title Course Type

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Official AKTU syllabus

This subject is on page 145, 146, 147 of the original AKTU PDF.

Official AKTU syllabus PDF ↗