List of Experiments / Activities
- Physical Pharmaceutics (Practical) Core Credit Hours Per Week (L-T-P) Max. Hours L T P
- 1-- --
- 45Maximum Marks SE ESE
- (Minimum 12 experiments must be performed)
- 1Determination of surface tension of given liquids by drop count method and drop weight method.
- 2Determination of critical micellar concentration (CMC) of surfactants.
- 3viscometer.
- 4Determination of HLB value of a surfactant.
- 5Calculation of isotonicity by different methods (Sodium Chloride Equivalent Method).
- 6Determination of particle size and particle size distribution using sieving method.
- 7Determination of particle size and particle size distribution using microscopic method.
- 8Determination of densities and derived properties of powders (bulk density, tapped
- 9Determination of angle of repose and influence of glidants on angle of repose.
- 10Determination of solubility of a drug at different pH/buffer systems at room temperature.
- 11Determination of partition coefficient of a drug in n-octanol and water system.
- 12Determination of partition coefficient of a drug in benzene and water system.
- 13Determination of critical solution temperature and composition of phenol water system.
- 14Determination of specific surface area of charcoal by adsorption of acetic acid on activated charcoal.
- 15Determination of buffer capacity at various stages of titration of a weak acid against a strong base and determination of pKa.
- Note: Compare the values of various physicochemical properties with marketed formulations wherever possible.
Course Objectives
- The objectives of this course are to:
- Introduce basic laboratory techniques for determining physicochemical properties such as surface tension, viscosity, and density in pharmaceutical systems.
- Develop understanding of interfacial phenomena and surfactant behavior, including micelles, critical micellar concentration (CMC), and HLB in formulation design.
- Train students in evaluating disperse systems through sedimentation studies and the effect of suspending agents.
- Provide practical experience in powder characterization, including particle size distribution, density, flow properties, porosity, and the role of glidants.
- Develop skills in determining solubility, partition coefficient, buffer capacity, and related equilibria relevant to drug formulation.
Course Outcomes (COs)
After completion of the course student will be able to:
- CO1Demonstrate practical knowledge of principles and procedures involved in measuring surface tension, viscosity, density, and related physical properties using standard laboratory apparatus.
- CO2Determine and interpret surfactant-related parameters such as CMC and HLB and explain their significance in formulation stability and performance.
- CO3Conduct experiments and analyze results related to sedimentation volume and evaluate the influence of type and concentration of suspending agents on dispersion stability.
- CO4Evaluate micromeritic and flow properties of powders by determining particle size repose, true density, and porosity, and interpret the effect of glidants.
- CO5Perform and assess experiments on solubility, partition coefficient, critical solution temperature, adsorption studies, and buffer capacity, and apply findings to formulation decisions.
Recommended References (Preferably latest editions)
- Sinko, P. J. Lippincott Williams & Wilkins.
- Aulton, M. E. and Taylor, K. M. G. Manufacture of Medicines. Elsevier.
- Lachman, L., Lieberman, H. A. and Kanig, J. L. The Theory and Practice of Industrial Pharmacy. CBS Publishers & Distributors.
- Allen, L. V., Popovich, N. G. and Ansel, H. C. and Drug Delivery Systems. Lippincott Williams & Wilkins.
- Cooper, S. J. and Gunn, C. CBS Publishers & Distributors. Course Code* Course Title* Course Type
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