alexa Abstract | Development and validation of HPLC method for the determination of pregabalin in capsules Highly accessed article

Indian Journal of Pharmaceutical Sciences
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A simple, precise, specifi c, and accurate reverse phase HPLC method has been developed for the determination of pregabalin in capsule dosage form. The chromatography was set on Hypersil BDS, C8, 150×4.6 mm, 5 μm column using photodiode array detector. The mobile phase consisting of phosphate buffer pH 6.9 and acetonitrile in the ratio of 95:05 with fl ow rate of 1 ml/min. The method was validated according to ICH guidelines with respect to specifi city, linearity, accuracy, precision and robustness. Lower limit of quantifi cation is 0.6 mg/l. The pregabalin sample solution was found to be stable at room temperature for about 26 h.

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Author(s): GB Kasawar MN Farooqui


Method development, pregabalin, RP-HPLC, validation

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