alexa Development and Validation of a Rapid High-Performance Liquid Chromatography Method with UV Detection for the Determination of Vancomycin in Mouse Plasma | Abstract
ISSN: 2157-7064

Journal of Chromatography & Separation Techniques
Open Access

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Research Article

Development and Validation of a Rapid High-Performance Liquid Chromatography Method with UV Detection for the Determination of Vancomycin in Mouse Plasma

Krishna Muppidi1, Andrew S. Pumerantz2, Guru Betageri1 and Jeffrey Wang1*

1Department of Pharmaceutical Sciences, College of Pharmacy, Western University of Health Sciences, USA

2Division of Infectious Disease, Department of Internal Medicine, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, USA

*Corresponding Author:
Jeffrey Wang
Department of Pharmaceutical Sciences
College of Pharmacy
Western University of Health Sciences
309 E. 2nd Street, Pomona
CA 91766, USA
E-mail: [email protected]

Received Date: December 07, 2012; Accepted Date: January 27, 2013; Published Date: January 29, 2013

Citation: Muppidi K, Pumerantz AS, Betageri G, Wang J (2013) Development and Validation of a Rapid High-Performance Liquid Chromatography Method with UV Detection for the Determination of Vancomycin in Mouse Plasma. J Chromat Separation Techniq 4:165. doi:10.4172/2157-7064.1000165

Copyright: © 2013 Muppidi K, 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

rapid high-performance liquid chromatography (HPLC) method for the quantification of vancomycin in mouse plasma samples was developed and validated. Norvancomycin was used as the internal standard. Chromatographic separation was achieved on a Vydac C18 column (4.6×50 mm, 3 μm particle size) and the detection was made at 214 nm. A gradient elution was programmed with the mobile phases of 0.1% v/v trifluoroacetic acid (A) and 95:5 v/v acetonitrile: 0.1% TFA (B) and a flow rate of 1 ml/min. The total run time was 15 min. The calibration curve was linear over the range of 0.1-20 μg/ml, with a correlation coefficient (r) higher than 0.997 and the lower limit of quantitation (LLOQ) of 0.1 μg /ml. The intra-day accuracy values were between 90 and 112% and the inter-day ones ranged from 96 to 104%. Precision values ranged from 1.7 to 9.5% for intra-day and 6.3 to 9.4% for inter-day. Stability studies under normal laboratory conditions without significant loss of the drug. The assay was successfully applied to the pharmacokinetics and bio-distribution study of novel formulations of vancomycin in mice.

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