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Pharmaceutical industry throught the world are bound by ICH quality guidelines. A quality unit of industry ensures to release of high purity drugs. Development of validated analytical methods in first step in this direction. A chromatographic method was developed for the estimation of pregabalin in pharmaceutical formulations. Drug is used for the treatment of nervous disorders in adults. The method involves Phenomenox-C18 column and mobile phase composition of acetate buffer and methanol (50:50, v/v). The wavelength of detection is 210 nm. The method is accurate and can apply for quality control samples in pharmaceutical formulations.
This research focuses primarily on novel analytical experiments which the author has developed using chromatographic technique as a reliable tool to conventional methods. This method evaluates the purity and safety of different brands of Pregabalin tablets available in the market. The method is selective, free from interference of excepients, further successfully validated as per ICH quality guideline. The reported method is reproducible and accurate (99.5- 100%), reported time period of the method is less than 10 minutes. The reported method is analytical friendly, affordable and can easily adaptable to quality control laboratories of pharma industry and research institutes.

Journal Name: International Journal of Pharmaceutical Sciences Review and Research , Volume Number: 4(7) , Page Number: 2782


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