RP – HPLC Method Development and Validation for Simultaneous Estimation of Irbesartan, Amlodipine and Hydrochlorothiazide in Bulk and Tablet Dosage Forms

Journal Title: Journal of Pharmaceutical and Medicinal Chemistry - Year 2017, Vol 3, Issue 2

Abstract

A reverse phase high performance liquid chromatographic method has been developed for the simultaneous estimation of Irbesartan, Amlodipine besylate and hydrochlorothiazide in bulk and Pharmaceutical formulation using RPC18 Column. The mobile phase (Acetonitrile: methanol: 50mM phosphate buffer adjusted to pH 3.2 with orthophosphoric acid) was pumped at a flow rate of 1.2 mL/min in the ratio of 20:50:30% v/v and the eluent was monitored at 250 nm. Linearity was obtained in the concentration range of 5 30 µg/ml for Amlodipine Besylate, 20 120 µg/ml for Irbesartan and 10 60 µg/ml for Hydrochlorothiazide. The method was statistically validated and RSD was found to be less than 2% indicating high degree of accuracy and precision of the proposed HPLC method. Due to its simplicity, rapidness, high precision and accuracy, the proposed HPLC method can be applied for determining Irbesartan, Amlodipine and hydrochlorothiazide in bulk and in pharmaceutical dosage form.

Authors and Affiliations

Gandla Kumaraswamy

Keywords

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  • EP ID EP469496
  • DOI 10.21088/jpmc.2395.6615.3217.4
  • Views 131
  • Downloads 0

How To Cite

Gandla Kumaraswamy (2017). RP – HPLC Method Development and Validation for Simultaneous Estimation of Irbesartan, Amlodipine and Hydrochlorothiazide in Bulk and Tablet Dosage Forms. Journal of Pharmaceutical and Medicinal Chemistry, 3(2), 89-97. https://europub.co.uk/articles/-A-469496