M.Pharmacy I Year I Semester (R22)
Students will know the pre-formulation studies, methodology, different excipients
used in solid dosage forms and their evaluation with references to production technologies. The students also know the optimization techniques and their applications in pharmaceutical industries.
Students shall explain the pre-formulation parameters, apply ICH guidelines and
evaluate drug, drug excipients compatibility. Students also explain about formulation and development, use of excipients in tablets, powders, capsules, micro-encapsules and coating techniques. They also learn and apply the statistical design in different formulations.
Pre-formulation: Goals of pre-formulation, solid state manipulation and characterization. pH dependent solubility of drug, equilibrium solubility, intrinsic dissolution of drug, particle size distribution. Flow of Powders: Physical properties and importance. Angle of repose, Cars index, compressibility, bulk density, tapped density.
Excipients used in various dosage forms like tablets, capsules, emulsions, suspensions, semisolids and sterile products. Knowledge of packing materials. Drug- excipient compatibility- Drug stability, factors affecting stability, stabilization methods.
Tablets: Types of tablets, granulation methods, highlighting operations such as mixing, drying, milling, blending, lubrication and compression. Tablet coating: Types of coating, steps involved in coating process- pan coating and fluid bed coating and problems associated with coating. Hard Gelatin Capsules: General principles and steps involved in the production of drug loaded hard gelatin capsules, filling operation, filling of powders, granules and pellets.
Dissolution: Principles of dissolution, factors influencing dissolution, official methods and apparatus. Dissolution of immediate release, controlled release and delayed release products.
Stability testing: Chemical degradation and preventive measures. Various stability testingconditions and use of stabilizers in packing
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