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ENHANCEMENT OF DISSOLUTION RATE OF CLOFIBRATE BY USING VARIOUS SOLID DISPERSION TECHNIQUES

Journal: Indo American Journal of Pharmaceutical Sciences (IAJPS) (Vol.2, No. 10)

Publication Date:

Authors : ; ;

Page : 1408-1422

Keywords : FT-IR; SEM Studies; Clofibrate; Hydroxyl propyl ?-Cyclodextrin; ?- Cyclodextrin; Solid dispersion; BCS class II Anti-hyperlipidemic drug.;

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Abstract

The aim of the present research work, Clofibrate a BCS class II Anti-hyperlipidemic drug belongs to fibrate class was formulated as solid dispersions by using various hydrophilic carriers to enhance the solubility, dissolution rate and oral bioavailability. Kneading technique is used to prepare solid dispersions of Clofibrate. Solid state characterization of solid dispersions is done by Differential Scanning Calorimetry, FourierTransform Infrared spectrometry and X-ray powder Diffraction studies, Scanning electron microscopy. The solid dispersions can be evaluated by in-vitro dissolution studies. To develop the solid oral dosage form (Tablets) with Clofibrate solid dispersions. To study the physical parameters of tablets prepared by direct compression, which includes hardness, friability, weight variation, and disintegration. To estimate the % drug content in the solid dispersions and the fabricated formulations. To evaluate the drug release from the tablets by in-vitro dissolution studies and to compare in-vitro dissolution profile of fabricated formulation with marketed formulation. Key words: FT-IR, SEM Studies, Clofibrate, Hydroxyl propyl ?-Cyclodextrin, ?- Cyclodextrin, Solid dispersion, BCS class II Anti-hyperlipidemic drug.

Last modified: 2015-11-07 13:36:04