FORMULATION AND EVALUATION OF BILAYERMATRIX TABLET OF PIOGLITAZONE HCL METFORMIN HCL USP 15MG&500MG
Kranthi Kumar Kotta, M Narasimha reddy, K. Sampath Kumar
Abstract
Kranthi Kumar Kotta, M Narasimha reddy, K. Sampath Kumar
Abstract
ABSTRACT The aim of present study was to design the concept of bilayered tablets containing Pioglitazone hydrochloride for immediate release using cross Povidone as super disintegrant and Metformin hydrochloride for sustained release using poly ethylene oxide (PEO-303) as matrix forming polymer. The tablets were evaluated for physicochemical properties. All the values are found to be satisfactory. In vitro release studies were carried out as per USP in pH 1.2 and phosphate buffer pH 6.8 using the USP apparatus II. The release kinetics of Metformin hydrochloride was evaluated using the regression coefficient analysis. The formulated tablets (F5) shows first order release and diffusion was the dominant mechanism of drug release. The polymer Polyethylene oxide (PEO- 303) had significant effect on the release of Metformin HCl matrix tablets (F5).Thus formulated bilayer tablets proved immediate release of Pioglitazone and Metformin HCl as sustained release over a period of 12 hours. The stability studies and FT-IR studies were also indicating the absence of strong interactions between the components and suggesting drug-excipient compatibility in all the formulations examined. Keywords: Bilayered tablets, Sustained release, Metformin HCl, Pioglitazone HCl, Matrix tablets, PEO-303.
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ABSTRACT The aim of present study was to design the concept of bilayered tablets containing Pioglitazone hydrochloride for immediate release using cross Povidone as super disintegrant and Metformin hydrochloride for sustained release using poly ethylene oxide (PEO-303) as matrix forming polymer. The tablets were evaluated for physicochemical properties. All the values are found to be satisfactory. In vitro release studies were carried out as per USP in pH 1.2 and phosphate buffer pH 6.8 using the USP apparatus II. The release kinetics of Metformin hydrochloride was evaluated using the regression coefficient analysis. The formulated tablets (F5) shows first order release and diffusion was the dominant mechanism of drug release. The polymer Polyethylene oxide (PEO- 303) had significant effect on the release of Metformin HCl matrix tablets (F5).Thus formulated bilayer tablets proved immediate release of Pioglitazone and Metformin HCl as sustained release over a period of 12 hours. The stability studies and FT-IR studies were also indicating the absence of strong interactions between the components and suggesting drug-excipient compatibility in all the formulations examined. Keywords: Bilayered tablets, Sustained release, Metformin HCl, Pioglitazone HCl, Matrix tablets, PEO-303.
Key concepts: Pioglitazone, Metformin Hydrochloride, Metformin, Chemistry, Polyethylene oxide, Pharmacology, Dosage form, Chromatography