Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/249650 |
Resumo: | Quercitrin, a glycosylated form of the flavonoid quercetin, is one of the major constituents of Copaifera langsdorffii leaves and potentially contributes to the medicinal properties reported for this plant species, including the treatment and prevention of kidney stones. To better understand the pharmacokinetics of quercitrin, a simple, rapid, and sensitive ultra fast liquid chromatography−tandem mass spectrometry method was developed and validated for the quantification of quercitrin in rat plasma and applied to a tissue distribution study. Sample preparation involved simple liquid−liquid extraction by ethyl acetate with high efficiency, using afzelin as internal standard. The chromatographic separation was performed on a Phenomenex Synergi Polar-RP (100 × 3.0 mm2, 2.5 μm), with a gradient elution of acetonitrile and 0.5% formic acid in water. The mass spectrometry analysis was conducted in negative ionization mode with multiple reaction monitoring transitions at m/z 447 → 300 for quercitrin and m/z 431 → 281 for afzelin. The method showed linearity in the concentration range of 5−100 ng/mL (r2 > 0.9959) and the lower limit of quantification was 5 ng/mL. The intraday and interday precision (relative standard deviation) were less than 10.73%, whereas the accuracy ranged from 81.4 to 111.0%. The extraction recovery, stability, matrix effect, and integrity dilution involved in the method were also validated. In addition, tissue distribution was assessed after an intravenous administration of 1 mg/kg quercitrin. This is the first report quantifying quercitrin in kidneys, demonstrating that the free tissue/plasma ratio was 23.7. |
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Costa, Juliana de Carvalho daMotta, Erick Vicente da SilvaBarreto, FabianoAraújo, Bibiana Verlindo deDerendorf, HartmutBastos, Jairo Kenupp2022-10-03T04:49:13Z20192470-1343http://hdl.handle.net/10183/249650001149048Quercitrin, a glycosylated form of the flavonoid quercetin, is one of the major constituents of Copaifera langsdorffii leaves and potentially contributes to the medicinal properties reported for this plant species, including the treatment and prevention of kidney stones. To better understand the pharmacokinetics of quercitrin, a simple, rapid, and sensitive ultra fast liquid chromatography−tandem mass spectrometry method was developed and validated for the quantification of quercitrin in rat plasma and applied to a tissue distribution study. Sample preparation involved simple liquid−liquid extraction by ethyl acetate with high efficiency, using afzelin as internal standard. The chromatographic separation was performed on a Phenomenex Synergi Polar-RP (100 × 3.0 mm2, 2.5 μm), with a gradient elution of acetonitrile and 0.5% formic acid in water. The mass spectrometry analysis was conducted in negative ionization mode with multiple reaction monitoring transitions at m/z 447 → 300 for quercitrin and m/z 431 → 281 for afzelin. The method showed linearity in the concentration range of 5−100 ng/mL (r2 > 0.9959) and the lower limit of quantification was 5 ng/mL. The intraday and interday precision (relative standard deviation) were less than 10.73%, whereas the accuracy ranged from 81.4 to 111.0%. The extraction recovery, stability, matrix effect, and integrity dilution involved in the method were also validated. In addition, tissue distribution was assessed after an intravenous administration of 1 mg/kg quercitrin. This is the first report quantifying quercitrin in kidneys, demonstrating that the free tissue/plasma ratio was 23.7.application/pdfengACS Omega. Washington. Vol. 4, no. 2 (2019), p. 3527−3533FlavonoidesFarmacocinéticaPlasmaExtractionFlavonoidsPharmacokineticsPlasmaRodent modelsDevelopment and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution studyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001149048.pdf.txt001149048.pdf.txtExtracted Texttext/plain34669http://www.lume.ufrgs.br/bitstream/10183/249650/2/001149048.pdf.txte2ea2148d6a4e68a406745afae8f2036MD52ORIGINAL001149048.pdfTexto completo (inglês)application/pdf2243179http://www.lume.ufrgs.br/bitstream/10183/249650/1/001149048.pdf93168f18f3101a4a2ff3fe1b9a5de139MD5110183/2496502022-10-04 05:01:41.040841oai:www.lume.ufrgs.br:10183/249650Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2022-10-04T08:01:41Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
title |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
spellingShingle |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study Costa, Juliana de Carvalho da Flavonoides Farmacocinética Plasma Extraction Flavonoids Pharmacokinetics Plasma Rodent models |
title_short |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
title_full |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
title_fullStr |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
title_full_unstemmed |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
title_sort |
Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study |
author |
Costa, Juliana de Carvalho da |
author_facet |
Costa, Juliana de Carvalho da Motta, Erick Vicente da Silva Barreto, Fabiano Araújo, Bibiana Verlindo de Derendorf, Hartmut Bastos, Jairo Kenupp |
author_role |
author |
author2 |
Motta, Erick Vicente da Silva Barreto, Fabiano Araújo, Bibiana Verlindo de Derendorf, Hartmut Bastos, Jairo Kenupp |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Costa, Juliana de Carvalho da Motta, Erick Vicente da Silva Barreto, Fabiano Araújo, Bibiana Verlindo de Derendorf, Hartmut Bastos, Jairo Kenupp |
dc.subject.por.fl_str_mv |
Flavonoides Farmacocinética Plasma |
topic |
Flavonoides Farmacocinética Plasma Extraction Flavonoids Pharmacokinetics Plasma Rodent models |
dc.subject.eng.fl_str_mv |
Extraction Flavonoids Pharmacokinetics Plasma Rodent models |
description |
Quercitrin, a glycosylated form of the flavonoid quercetin, is one of the major constituents of Copaifera langsdorffii leaves and potentially contributes to the medicinal properties reported for this plant species, including the treatment and prevention of kidney stones. To better understand the pharmacokinetics of quercitrin, a simple, rapid, and sensitive ultra fast liquid chromatography−tandem mass spectrometry method was developed and validated for the quantification of quercitrin in rat plasma and applied to a tissue distribution study. Sample preparation involved simple liquid−liquid extraction by ethyl acetate with high efficiency, using afzelin as internal standard. The chromatographic separation was performed on a Phenomenex Synergi Polar-RP (100 × 3.0 mm2, 2.5 μm), with a gradient elution of acetonitrile and 0.5% formic acid in water. The mass spectrometry analysis was conducted in negative ionization mode with multiple reaction monitoring transitions at m/z 447 → 300 for quercitrin and m/z 431 → 281 for afzelin. The method showed linearity in the concentration range of 5−100 ng/mL (r2 > 0.9959) and the lower limit of quantification was 5 ng/mL. The intraday and interday precision (relative standard deviation) were less than 10.73%, whereas the accuracy ranged from 81.4 to 111.0%. The extraction recovery, stability, matrix effect, and integrity dilution involved in the method were also validated. In addition, tissue distribution was assessed after an intravenous administration of 1 mg/kg quercitrin. This is the first report quantifying quercitrin in kidneys, demonstrating that the free tissue/plasma ratio was 23.7. |
publishDate |
2019 |
dc.date.issued.fl_str_mv |
2019 |
dc.date.accessioned.fl_str_mv |
2022-10-03T04:49:13Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/249650 |
dc.identifier.issn.pt_BR.fl_str_mv |
2470-1343 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001149048 |
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2470-1343 001149048 |
url |
http://hdl.handle.net/10183/249650 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
ACS Omega. Washington. Vol. 4, no. 2 (2019), p. 3527−3533 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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