A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma

A rapid, selective and sensitive high performance liquid chromatographic method for the estimation of nevirapine in human plasma has been developed. Chromatography was carried out on a Hypersil BDS C18 column using a mixture of ammonium acetate buffer (pH 4.0 ± 0.05) and acetonitrile (85:15 v/v) as...

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Main Authors: C. H. Venkata Kumar, D. Ananth Kumar, J. V. L. N. Seshagiri Rao
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2010/262601
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author C. H. Venkata Kumar
D. Ananth Kumar
J. V. L. N. Seshagiri Rao
author_facet C. H. Venkata Kumar
D. Ananth Kumar
J. V. L. N. Seshagiri Rao
author_sort C. H. Venkata Kumar
collection DOAJ
description A rapid, selective and sensitive high performance liquid chromatographic method for the estimation of nevirapine in human plasma has been developed. Chromatography was carried out on a Hypersil BDS C18 column using a mixture of ammonium acetate buffer (pH 4.0 ± 0.05) and acetonitrile (85:15 v/v) as the mobile phase. The eluents were monitored for the drug by UV detection at 254 nm. Oxcarbazepine was used as an internal standard for this study. The retention times for nevirapine and oxcarbazepine were found to be 7.2 and 14.7 min respectively. The method was found to be linear in the concentration range of 50 ng/mL to 5003.7 ng/mL. The method was validated as per FDA guidelines and was found to be suitable for bioequivalence and pharmacokinetic studies.
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spelling doaj-art-07bf1da5a8b548d59b04e12c52f238b22025-08-20T03:55:28ZengWileyE-Journal of Chemistry0973-49452090-98102010-01-017382182610.1155/2010/262601A New Validated RP- HPLC Method for the Determination of Nevirapine in Human PlasmaC. H. Venkata Kumar0D. Ananth Kumar1J. V. L. N. Seshagiri Rao2Pharmaceutical Analysis and Quality Assurance Division, A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam-530003, IndiaPharmaceutical Analysis and Quality Assurance Division, A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam-530003, IndiaPharmaceutical Analysis and Quality Assurance Division, A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam-530003, IndiaA rapid, selective and sensitive high performance liquid chromatographic method for the estimation of nevirapine in human plasma has been developed. Chromatography was carried out on a Hypersil BDS C18 column using a mixture of ammonium acetate buffer (pH 4.0 ± 0.05) and acetonitrile (85:15 v/v) as the mobile phase. The eluents were monitored for the drug by UV detection at 254 nm. Oxcarbazepine was used as an internal standard for this study. The retention times for nevirapine and oxcarbazepine were found to be 7.2 and 14.7 min respectively. The method was found to be linear in the concentration range of 50 ng/mL to 5003.7 ng/mL. The method was validated as per FDA guidelines and was found to be suitable for bioequivalence and pharmacokinetic studies.http://dx.doi.org/10.1155/2010/262601
spellingShingle C. H. Venkata Kumar
D. Ananth Kumar
J. V. L. N. Seshagiri Rao
A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
E-Journal of Chemistry
title A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
title_full A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
title_fullStr A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
title_full_unstemmed A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
title_short A New Validated RP- HPLC Method for the Determination of Nevirapine in Human Plasma
title_sort new validated rp hplc method for the determination of nevirapine in human plasma
url http://dx.doi.org/10.1155/2010/262601
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