PURPOSE: The aim of the study was to formulate different proportion of Lamivudine: Methocel K15M with mannitol formulations, in order to investigation the effect of polymer proportion and diluent (mannitol and avicel) on the drug release mechanism. Lamivudine, an anti-HIV agent, was used as a model drug to evaluate its release characteristics from different matrices. METHOD: Matrix tablets of Lamivudine were prepared by direct compression process using methocel K15M CR polymer mannitol and avicel as filler. In vitro release studies were performed using US Pharmacopeia type 1 apparatus (basket method) in 900 ml of pH 1.2 and pH 6.8 phosphate buffer at 100 rpm for 8 hours. Scanning Electron Microscopy (SEM) was used to evaluate and surface properties of the matrices. Drug release was analyzed according to their kinetic models. A One-way analysis of variance (ANOVA) was used to interpret the result. RESULTS: Statistically significant differences were found among the drug release profile from different formulations. Higher proportion of polymeric content (30% of the total tablet weight) in the matrix, release was extended > 8 hours due to increased tortuosity and decreased porosity. At lower proportion of polymeric content (10% of the total tablet weight), the rate of drug release was elevated. Two formulations showed drug release is more controlled. The release mechanism was explored and explained with zero order, first order, Higuchi and Korsmeyer and Hixon-Crowell equations. CONCLUSION: The release kinetics was found to be governed by the type and content of the excipients (polymer or filler, mannitol). By suitable modulation could be developed controlled delivery of such type of drug.
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