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OPHTHALMIC NANOPARTICLES DRUG DELIVERY SYSTEMS (Ezine Ready) - My sait

OPHTHALMIC NANOPARTICLES DRUG DELIVERY SYSTEMS (Ezine Ready)

In addition, small particles size and large surface area readily result in limited drug loading and burst release. These practical problems have to be overcome before nanoparticles can be used clinically or made commercially available. The present review details the latest development of nanoparticulate drug delivery systems, surface modification issues, drug loading strategies, release control and potential applications of nanoparticles.   Preparation of nanoparticles Methods: Nanoparticles can be prepared from a variety of materials such as proteins, polysaccharides and synthetic polymers. The selection of matrix materials is dependent on many factors Including, Size of nanoparticles required.Inherent properties of the drug, e.g., aqueous solubility and stability.Surface characteristics such as charge and permeability.Degree of biodegradability, biocompatibility and toxicity. Drug release profile desired.Antigenicity of the final product.Methods: Dispersion of preformed polymersSolvent evaporation methodSpontaneous emulsification or solvent diffusion MethodPolymerization methodCoacervation or ionic gelation methodProduction of nanoparticles using supercritical fluid   POLY METHYL METHACRYLATE (PMMA) (ACRYLIC)    Structure of Polymethyl MethacrylateMolecular formula  (C5O2H8)nINTRODUCTIONPoly (methyl methacrylate) (PMMA) poly (methyl 2-methylpropenoate) is a thermoplastic and transparent plastic. Chemically, it is the synthetic polymer of methyl methacrylate. PMMA is often used as an alternative to glass, and in competition with polycarbonate (PC).

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