Method Development and Validation for Analysis of Carbidopa in Bulk Drug and Formulations.by RP-HPLC

Abstract

A simple, precise and accurate RP-HPLC method was developed and validated for rapid assay of Carbidopa in tablet dosage form. Isocratic elution at a flow rate of 1.0ml/min was employed on a symmetry C18 (250×4.6mm, 5μm in particle size) at ambient temperature. The mobile phase consisted of methanol: KH2PO4: 75:25 (V/V). The UV detection wavelength was 262 nm and 20μl sample was injected. The retention time for Carbidopa was 1.48 min. The percentage RSD for precision and accuracy of the method was found to be less than 2%. The method was validated as per the ICH guidelines. The method was successfully applied for routine analysis of Carbidopa in tablet dosage form and bulk drug.

Issue

2011 Volume-01

Article Subject

Biotechnology

Keywords

Carbidopa, RP-HPLC, UV detection, recovery, precise, 262 nm

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