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Validated RP-HPLC Method for Simultaneous Determination of Telmisartan and Hydrochlorothiazide in Pharmaceutical Formulation 

Authors: Leena R. Bhat a;  Rahul K. Godge a;  Asfak T. Vora a; Mrinalini C. Damle a
Affiliation:   a Department of Pharmaceutical Analysis, A.I.S.S.M.S. College of Pharmacy, Maharashtra, India
DOI: 10.1080/10826070701632774
Publication Frequency: 20 issues per year
Published in: journal Journal of Liquid Chromatography & Related Technologies, Volume 30, Issue 20 December 2007 , pages 3059 - 3067
Subject: Chromatography;
Formats available: HTML (English) : PDF (English)
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Abstract

A simple, selective, and precise reverse phase high performance liquid chromatographic method has been developed for the simultaneous determination of Telmisartan and hydrochlorothiazide from pharmaceutical formulation. The mobile phase consisted of methanol and acetonitrile (70:30 v/v) at a flow rate of 1 mL/min and the wavelength of detection was 270 nm. Rabeprazole was used as an internal standard. The retention times of Telmisartan, hydrochlorothiazide and rabeprazole were 1.79±0.01, 2.80±0.01, and 3.19±0.01 minutes, respectively. The developed method was validated according to ICH guidelines. The proposed method can be used for determination of these drugs in combined dosage forms.
Keywords: Telmisartan; Hydrochlorothiazide; Rabeprazole; RP-HPLC
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