alexa Development and Validation of Stability Indicating RP-UPLC Method for Simultaneous Determination in Fixed Dose Combination of Ezetimibe and Simvastatin
ISSN: 2157-7064

Journal of Chromatography & Separation Techniques
Open Access

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Research Article

Development and Validation of Stability Indicating RP-UPLC Method for Simultaneous Determination in Fixed Dose Combination of Ezetimibe and Simvastatin

Seshukumar Devu1, Abhishek Gupta2*, Kona S Srinivas2, Ravi Shankar Gupta2 and Vinod Prasad Semwal2

1School of Pharmaceutical Sciences and Technologies, Jawaharlal Nehru Technological University, Kakinada, India

2Department of Analytical Chemistry, Daiichi Sankyo India Pharma Pvt.Ltd., Gurgaon, India

*Corresponding Author:
Mr. Abhishek Gupta
Daiichi Sankyo Research Centre in India, Plot-20
Sector-18, Gurgaon, India
E-mail: [email protected]

Received date: July 09, 2012; Accepted date: July 20, 2012; Published date: July 28, 2012

Citation: Seshukumar D, Abhishek G, Srinivas KS, Ravi Shankar G, Vinod Prasad S (2012) Development and Validation of Stability Indicating RP-UPLC Method for Simultaneous Determination in Fixed Dose Combination of Ezetimibe and Simvastatin. J Chromat Separation Techniq 3:131. doi:10.4172/2157-7064.1000131

Copyright: © 2012 Seshukumar D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

A stability indicating UPLC method was developed and validated for the simultaneous determination of fixed dose combination of ezetimibe and simvastatin in bulk drug. The developed method was successfully applied to the simultaneous quantitative analysis of the title drugs in tablet dosage form. The chromatographic separation was performed on Kromasil Eternity TM C 18 UHPLC column (2.5 μm, 2.1 mm x 50 mm) using gradient elution of acetonitrile and ammonium acetate buffer (pH 6.70; 0.01 M) as mobile phase at a flow rate of 0.35 mL/min and column oven temperature of 40ºC. UV detection was carried out using a UV-PDA detector at 235 nm. Total run time was 3.5 min within which main compounds and their degradation products were separated. The method was validated for accuracy, repeatability, reproducibility and robustness. Linearity, LOD and LOQ were established for ezetimibe and simvastatin.

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