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Chromatography Research InternationalVolume 2013 2013, Article ID 963595, 9 pages

Research Article

Department of Pharmaceutical Analysis, Hindu College of Pharmacy, Amaravathi Road, Guntur 522 002, India

Department of Pharmaceutical Analysis, K.V.S.R Siddhartha College of Pharmaceutical Sciences, Vijayawada 520 101, India

Received 12 February 2013; Revised 18 March 2013; Accepted 19 March 2013

Academic Editor: Antonio Martín-Esteban

Copyright © 2013 Singaram Kathirvel and Garikapati Devalarao. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

A sensitive, precise, specific, linear, and stability-indicating gradient HPLC method was developed for the estimation of doripenem in active pharmaceutical ingredient API and in injectable preparations. Chromatographic separation was achieved on C18 stationary phase with a mobile phase gradient consisting of acetonitrile, methanol, and pH 5.2 phosphate buffer. The mobile phase flow rate was 0.8 mL-min, and the eluted compounds were monitored at 210 nm. The method is linear over the range of 0.335 to 76.129 µg-mL. The correlation coefficient was found to be 0.999. The numbers of theoretical plates and tailing factor for doripenem were 53021 and 0.9, respectively. Doripenem was subjected to the International Conference on Harmonization ICH prescribed hydrolytic acid, base, and neutral, oxidative, photolytic, and thermal stress conditions. Among all the above-mentioned conditions, the drug was found to be stable under photolytic degradation. Peak homogeneity data for doripenem in the chromatograms from the stressed samples obtained by use of the photodiode array detector demonstrated the specificity of the method for analysis of doripenem in presence of the degradation products. The performance of the method was validated according to the present ICH guidelines for specificity, limit of detection, limit of quantification, linearity, accuracy, precision, and robustness.





Autor: Singaram Kathirvel and Garikapati Devalarao

Fuente: https://www.hindawi.com/



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