Development and validation of a sensitive UFLC−MS/MS method for quantification of quercitrin in plasma : application to a tissue distribution study

Detalhes bibliográficos
Autor(a) principal: Costa, Juliana de Carvalho da
Data de Publicação: 2019
Outros Autores: Motta, Erick Vicente da Silva, Barreto, Fabiano, Araújo, Bibiana Verlindo de, Derendorf, Hartmut, Bastos, Jairo Kenupp
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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spelling 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
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dc.identifier.issn.pt_BR.fl_str_mv 2470-1343
dc.identifier.nrb.pt_BR.fl_str_mv 001149048
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv ACS Omega. Washington. Vol. 4, no. 2 (2019), p. 3527−3533
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