Mukund G. Tawar

ABSTRACTDevelopment, and production of pharmaceutical products. The authorized test methods that result from HPLC, UV processes are used by quality control laboratories to make sure the Identity, characteristics, purity, potency, and performance of drug products.  Analytical methods development ought to be validated to give reliable data for regulatory submissions. This review gives information regarding various stages involved in development and validation of analytical methods like UV, HPLC. Rapid increase in pharmaceutical industries and production of drug in various parts of the world has brought a rise in demand for new analytical techniques in the pharmaceutical industries. As a result, analytical method development has developed into the basic activity of analysis. Recent development in analytical methods has been result from the advancement of analytical instruments.  Keywords : High performance liquid chromatography (HPLC); (LOQ) UV-visible spectrophotometer. limit of detection (LOD); Limit of quantitation

ABSTRACTThe aims of review are the latest research development of the lipid based carriers according to the recent relevant literatures. Each preparation of the lipid based microparticles (SLMs) has advantages and disadvantages. The SLMs is an excellent drug delivery system and has broad prospects in the pharmaceutical field. This review discusses the advantages, therapeutic application of SLMs, various techniques of preparation, and different routes of administration, material use and characterization of solid lipid microparticles. Keywords: SLM, Production technique, Lipid based carrier, Pharmaceutical application.