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Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma

A rapid and simple high performance liquid chromatography (HPLC) method with a UV detection (241 nm) was developed and validated for estimation of eplerenone from spiked human plasma. The analyte and the internal standard (valdecoxib) were extracted with a mixture of dichloromethane and diethyl ethe...

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Detalles Bibliográficos
Autores principales: Gide, Paraag, Sonawane, Sandeep, Chitnis, Abhishek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760755/
https://www.ncbi.nlm.nih.gov/pubmed/29403773
http://dx.doi.org/10.1016/j.jpha.2012.04.006
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author Gide, Paraag
Sonawane, Sandeep
Chitnis, Abhishek
author_facet Gide, Paraag
Sonawane, Sandeep
Chitnis, Abhishek
author_sort Gide, Paraag
collection PubMed
description A rapid and simple high performance liquid chromatography (HPLC) method with a UV detection (241 nm) was developed and validated for estimation of eplerenone from spiked human plasma. The analyte and the internal standard (valdecoxib) were extracted with a mixture of dichloromethane and diethyl ether. The chromatographic separation was performed on a HiQSil C-18HS column (250 mm×4.6 mm, 5 μm) with a mobile phase consisting of acetonitrile:water (50:50, v/v) at flow rate of 1 mL/min. The calibration curve was linear in the range 100–3200 ng/mL and the heteroscedasticity was minimized by using weighted least squares regression with weighting factor 1/X.
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spelling pubmed-57607552018-02-05 Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma Gide, Paraag Sonawane, Sandeep Chitnis, Abhishek J Pharm Anal Article A rapid and simple high performance liquid chromatography (HPLC) method with a UV detection (241 nm) was developed and validated for estimation of eplerenone from spiked human plasma. The analyte and the internal standard (valdecoxib) were extracted with a mixture of dichloromethane and diethyl ether. The chromatographic separation was performed on a HiQSil C-18HS column (250 mm×4.6 mm, 5 μm) with a mobile phase consisting of acetonitrile:water (50:50, v/v) at flow rate of 1 mL/min. The calibration curve was linear in the range 100–3200 ng/mL and the heteroscedasticity was minimized by using weighted least squares regression with weighting factor 1/X. Xi'an Jiaotong University 2012-10 2012-04-24 /pmc/articles/PMC5760755/ /pubmed/29403773 http://dx.doi.org/10.1016/j.jpha.2012.04.006 Text en © 2012 Xi'an Jiaotong University http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Gide, Paraag
Sonawane, Sandeep
Chitnis, Abhishek
Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title_full Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title_fullStr Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title_full_unstemmed Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title_short Development and validation of RP-HPLC method for estimation of eplerenone in spiked human plasma
title_sort development and validation of rp-hplc method for estimation of eplerenone in spiked human plasma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760755/
https://www.ncbi.nlm.nih.gov/pubmed/29403773
http://dx.doi.org/10.1016/j.jpha.2012.04.006
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