Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode

Detalhes bibliográficos
Autor(a) principal: Piovesan,Jamille V.
Data de Publicação: 2014
Outros Autores: Spinelli,Almir
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300015
Resumo: A carbon-paste electrode modified with the polymer poly(vinylpyrrolidone) was evaluated through electrochemical studies and the electroanalytical determination of quercetin. For this electrode, cyclic voltammograms of quercetin showed three oxidation peaks at +0.32, +0.78 and +1.04 V. The electro-oxidation associated with the first peak leads to the formation of the corresponding ortho-quinone, which can be reduced under favorable experimental conditions. Under such conditions, the reaction is quasi-reversible and the process is diffusion-controlled. This behavior was exploited for the electroanalytical determination of quercetin by square-wave voltammetry. The calibration curve was linear in the concentration range of 0.5 to 5.5 µmol L-1 (R² = 0.998). The limits of detection and quantification obtained were 0.17 µmol L-1 and 0.52 µmol L-1, respectively. The sensor was successfully used for the determination of quercetin in a pharmaceutical sample. The accuracy of the results achieved with the sensor was evaluated through comparison with the results provided by the UV-Vis technique.
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spelling Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrodequercetincarbon-paste electrodepoly(vinylpyrrolidone)electroanalysisA carbon-paste electrode modified with the polymer poly(vinylpyrrolidone) was evaluated through electrochemical studies and the electroanalytical determination of quercetin. For this electrode, cyclic voltammograms of quercetin showed three oxidation peaks at +0.32, +0.78 and +1.04 V. The electro-oxidation associated with the first peak leads to the formation of the corresponding ortho-quinone, which can be reduced under favorable experimental conditions. Under such conditions, the reaction is quasi-reversible and the process is diffusion-controlled. This behavior was exploited for the electroanalytical determination of quercetin by square-wave voltammetry. The calibration curve was linear in the concentration range of 0.5 to 5.5 µmol L-1 (R² = 0.998). The limits of detection and quantification obtained were 0.17 µmol L-1 and 0.52 µmol L-1, respectively. The sensor was successfully used for the determination of quercetin in a pharmaceutical sample. The accuracy of the results achieved with the sensor was evaluated through comparison with the results provided by the UV-Vis technique.Sociedade Brasileira de Química2014-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300015Journal of the Brazilian Chemical Society v.25 n.3 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140019info:eu-repo/semantics/openAccessPiovesan,Jamille V.Spinelli,Almireng2014-03-19T00:00:00Zoai:scielo:S0103-50532014000300015Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-03-19T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
title Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
spellingShingle Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
Piovesan,Jamille V.
quercetin
carbon-paste electrode
poly(vinylpyrrolidone)
electroanalysis
title_short Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
title_full Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
title_fullStr Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
title_full_unstemmed Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
title_sort Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
author Piovesan,Jamille V.
author_facet Piovesan,Jamille V.
Spinelli,Almir
author_role author
author2 Spinelli,Almir
author2_role author
dc.contributor.author.fl_str_mv Piovesan,Jamille V.
Spinelli,Almir
dc.subject.por.fl_str_mv quercetin
carbon-paste electrode
poly(vinylpyrrolidone)
electroanalysis
topic quercetin
carbon-paste electrode
poly(vinylpyrrolidone)
electroanalysis
description A carbon-paste electrode modified with the polymer poly(vinylpyrrolidone) was evaluated through electrochemical studies and the electroanalytical determination of quercetin. For this electrode, cyclic voltammograms of quercetin showed three oxidation peaks at +0.32, +0.78 and +1.04 V. The electro-oxidation associated with the first peak leads to the formation of the corresponding ortho-quinone, which can be reduced under favorable experimental conditions. Under such conditions, the reaction is quasi-reversible and the process is diffusion-controlled. This behavior was exploited for the electroanalytical determination of quercetin by square-wave voltammetry. The calibration curve was linear in the concentration range of 0.5 to 5.5 µmol L-1 (R² = 0.998). The limits of detection and quantification obtained were 0.17 µmol L-1 and 0.52 µmol L-1, respectively. The sensor was successfully used for the determination of quercetin in a pharmaceutical sample. The accuracy of the results achieved with the sensor was evaluated through comparison with the results provided by the UV-Vis technique.
publishDate 2014
dc.date.none.fl_str_mv 2014-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300015
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140019
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.25 n.3 2014
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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