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Original Research Article | OPEN ACCESS

Quantitative Determination of Metformin Hydrochloride in Tablet Formulation Containing Croscarmellose Sodium as Disintegrant by HPLC and UV Spectrophotometry

P Umapathi1 , J Ayyappan2, Darlin S Quine3

1Department of Analytical Research and Development, Micro Labs Ltd, 67/68-A, Third Phase, Peenya Industrial Area, Bangalore 560 058; 2SASTRA University, Thanjavur, Tamil Nadu; 3PG and Research Department of Chemistry, Government Arts College, Chidambaram, India.

For correspondence:-  P Umapathi   Email: varasubio@rediffmail.com

Received: 18 May 2011        Accepted: 2 December 2011        Published: 21 February 2012

Citation: Umapathi P, Ayyappan J, Quine DS. Quantitative Determination of Metformin Hydrochloride in Tablet Formulation Containing Croscarmellose Sodium as Disintegrant by HPLC and UV Spectrophotometry. Trop J Pharm Res 2012; 11(1):107-116 doi: 10.4314/tjpr.v11i1.14

© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop and validate a suitable method for the assay of metformin hydrochloride (HCl) in tablets containing croscarmellose sodium as an additive.
Methods: Methanol and ethanol (99%) were assessed as solvents for sample preparation for the assay of metformin HCl in tablets containing croscarmellose sodium by high performance liquid chromatography (HPLC) and ultra violet spectrophotometric (UV) methods. The proposed method was subjected to validation tests.
Results: Recovery of metformin HCl from the placebo-spiked sample was 95.1 to 96.9 % as per BP and USP methods compared with 99.3 to 100.8 %  when analyzed by the proposed method. The use of methanol and ethanol as solvents resolved the problem of retention of metformin HCl by croscarmellose sodium in solution during the preparation of sample solution.
Conclusion: The modified UV and HPLC methods are suitable for the determination of metformin HCl in tablets both in the presence and absence of croscarmellose sodium. The method is specific, precise, accurate, robust, rugged and gives a linear response for the quantitative estimation of metformin HCl in tablet formulation.

Keywords: Tablets; Metformin HCl assay; Croscarmellose sodium; Ethanol; Methanol; HPLC, UV

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Thompson Reuters (ISI): 0.523 (2021)
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