Validated RP-HPLC Method for the Determination of Indapamide in Bulk and Tablet Dosage Form | Abstract

Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences and Computational Chemistry

ISSN: 0975-413X
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Validated RP-HPLC Method for the Determination of Indapamide in Bulk and Tablet Dosage Form

Author(s): Harpreet Kaur H Pannu, M. P. Mahajan, S. D. Sawant

A novel, simple and economic reverse phase high performance liquid chromatography (RP-HPLC) method has been developed for the estimation of Indapamide in bulk and tablet dosage form with greater precision and accuracy. Separation was achieved on C18 column (250X4.6mm i.d.,5μm) in isocratic mode using Acetonitrile:Methanol:Water in the ratio of 40:50:10 (v/v/v) as mobile phase, pumped in to the column at flow rate of 1.0 mL min−1and the detection of eluent from the column was carried out using variable wavelength UV detector at 242 nm. The total run time was 10 min and the column was maintained at ambient temperature. The retention time of Indapamide was 3.233 min. The standard curves were linear over the concentration range of 10-60 μg mL−1 with R2 9995 and the LOD and LOQ values for Indapamide were 0.52 μg mL−1and 0.78 μg mL−1, respectively. The percentage recovery was found to be 98.16 – 100.12%, the % RSD of intraday and inter day precision was found to be 0.4404 and 0.5588, respectively. The percentage amount of a marketed tablet formulation of Indapamide was found to be 99.12 %. The method was validated as per ICH guidelines. Validation studies demonstrated that the proposed RP-HPLC method is simple, specific, rapid, reliable and reproducible. Hence the proposed method can be applied for the routine quality control analysis of Indapamide in bulk and tablet dosage forms.


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