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The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection

A sensitive, specific, reproducible and optimized high performance liquid chromatography with fluorescence detection (HPLC-FLD) method for the determination of bergapten in rat plasma was established and applied to the pharmacokinetic and bioavailability study in rat after oral and intravenous admin...

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Autores principales: Yu, Xie-an, Azietaku, John Teye, Li, Jin, An, Mingrui, He, Jun, Hao, Jia, Cao, Jun, Chang, Yan-xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064970/
https://www.ncbi.nlm.nih.gov/pubmed/27795734
http://dx.doi.org/10.1186/s13065-016-0212-x
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author Yu, Xie-an
Azietaku, John Teye
Li, Jin
An, Mingrui
He, Jun
Hao, Jia
Cao, Jun
Chang, Yan-xu
author_facet Yu, Xie-an
Azietaku, John Teye
Li, Jin
An, Mingrui
He, Jun
Hao, Jia
Cao, Jun
Chang, Yan-xu
author_sort Yu, Xie-an
collection PubMed
description A sensitive, specific, reproducible and optimized high performance liquid chromatography with fluorescence detection (HPLC-FLD) method for the determination of bergapten in rat plasma was established and applied to the pharmacokinetic and bioavailability study in rat after oral and intravenous administration of bergapten. The method was also successfully applied to the excretion study of bergapten after an oral administration of bergapten at a dose of 15 mg kg(−1) to rats. The sample preparation was achieved using liquid–liquid extraction. Isoimperatorin was used as the internal standard (IS). The analytes were detected by using fluorescence detection at an excitation and emission wavelength of 288 and 478 nm, respectively. Using aqueous formic acid (0.1 %, v/v) and acetonitrile as the mobile phase, the chromatographic separation was achieved on a Hedera™ ODS column at a flow rate of 1 mL min(−1). The lower limit of quantitation (LLOQ) of bergapten was 2 ng mL(−1). The HPLC-FLD method was successfully applied to the pharmacokinetic, bioavailability and excretion study of bergapten in rats. [Figure: see text]
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spelling pubmed-50649702016-10-28 The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection Yu, Xie-an Azietaku, John Teye Li, Jin An, Mingrui He, Jun Hao, Jia Cao, Jun Chang, Yan-xu Chem Cent J Research Article A sensitive, specific, reproducible and optimized high performance liquid chromatography with fluorescence detection (HPLC-FLD) method for the determination of bergapten in rat plasma was established and applied to the pharmacokinetic and bioavailability study in rat after oral and intravenous administration of bergapten. The method was also successfully applied to the excretion study of bergapten after an oral administration of bergapten at a dose of 15 mg kg(−1) to rats. The sample preparation was achieved using liquid–liquid extraction. Isoimperatorin was used as the internal standard (IS). The analytes were detected by using fluorescence detection at an excitation and emission wavelength of 288 and 478 nm, respectively. Using aqueous formic acid (0.1 %, v/v) and acetonitrile as the mobile phase, the chromatographic separation was achieved on a Hedera™ ODS column at a flow rate of 1 mL min(−1). The lower limit of quantitation (LLOQ) of bergapten was 2 ng mL(−1). The HPLC-FLD method was successfully applied to the pharmacokinetic, bioavailability and excretion study of bergapten in rats. [Figure: see text] Springer International Publishing 2016-10-14 /pmc/articles/PMC5064970/ /pubmed/27795734 http://dx.doi.org/10.1186/s13065-016-0212-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yu, Xie-an
Azietaku, John Teye
Li, Jin
An, Mingrui
He, Jun
Hao, Jia
Cao, Jun
Chang, Yan-xu
The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title_full The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title_fullStr The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title_full_unstemmed The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title_short The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
title_sort pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064970/
https://www.ncbi.nlm.nih.gov/pubmed/27795734
http://dx.doi.org/10.1186/s13065-016-0212-x
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