Determination of quercetin in a pharmaceutical sample by square-wave voltammetry using a poly(vinylpyrrolidone)-modified carbon-paste electrode
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | |
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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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 |
format |
article |
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 |
_version_ |
1750318175752290304 |