Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application

A selective liquid chromatography-mass spectrometry (LC–MS) method for determination of febuxostat in rat plasma was developed and validated. After addition of midazolam as internal standard (IS), protein precipitation by acetonitrile was used as sample preparation, and chromatography involved Agile...

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Autores principales: Ding, Xitao, Zhang, Qingwei, Wang, Zhiyi, Lin, Guanyang
Formato: Articulo Comunicacion
Lenguaje:Inglés
Publicado: 2012
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/18144
http://www.latamjpharm.org/resumenes/31/2/LAJOP_31_2_2_4.pdf
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id I19-R120-10915-18144
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
LC-MS; febuxostat; pharmacokinetics;rat plasma
Farmacología
Farmacocinética
spellingShingle Farmacia
LC-MS; febuxostat; pharmacokinetics;rat plasma
Farmacología
Farmacocinética
Ding, Xitao
Zhang, Qingwei
Wang, Zhiyi
Lin, Guanyang
Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
topic_facet Farmacia
LC-MS; febuxostat; pharmacokinetics;rat plasma
Farmacología
Farmacocinética
description A selective liquid chromatography-mass spectrometry (LC–MS) method for determination of febuxostat in rat plasma was developed and validated. After addition of midazolam as internal standard (IS), protein precipitation by acetonitrile was used as sample preparation, and chromatography involved Agilent SB-C18 column (2.1 x150 mm, 5 μm) using 0.1% formic acid in water and acetonitrile as a mobile phase with gradient elution. Detection involved positive ion mode electrospray ionization (ESI), and selective ion monitoring (SIM) mode was used for quantification of target fragment ions m/z 317 for febuxostat and m/z 326 for midazolam (internal standard, IS). The assay was linear over the range of 10-2000 ng/mL for febuxostat, with a lower limit of quantitation (LLOQ) of 10 ng/mL for febuxostat. Intra- and inter-day RSDs were less than 15% and the accuracies were in the range of 93.8-111.9% for febuxostat. This developed method was successfully applied to determinate of febuxostat in rat plasma for pharmacokinetic study.
format Articulo
Comunicacion
author Ding, Xitao
Zhang, Qingwei
Wang, Zhiyi
Lin, Guanyang
author_facet Ding, Xitao
Zhang, Qingwei
Wang, Zhiyi
Lin, Guanyang
author_sort Ding, Xitao
title Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
title_short Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
title_full Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
title_fullStr Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
title_full_unstemmed Development and Validation of Liquid Chromatography-Mass Spectrometry Method for Determination of Febuxostat in Rat Plasma and its Application
title_sort development and validation of liquid chromatography-mass spectrometry method for determination of febuxostat in rat plasma and its application
publishDate 2012
url http://sedici.unlp.edu.ar/handle/10915/18144
http://www.latamjpharm.org/resumenes/31/2/LAJOP_31_2_2_4.pdf
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AT wangzhiyi developmentandvalidationofliquidchromatographymassspectrometrymethodfordeterminationoffebuxostatinratplasmaanditsapplication
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