Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry

Detalhes bibliográficos
Autor(a) principal: Reis,Alaécio P. dos
Data de Publicação: 2008
Outros Autores: Tarley,César R. T., Kubota,Lauro T.
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=S0103-50532008000800017
Resumo: The present work describes an analytical methodology for simultaneous determination of ascorbic acid (AA) and uric acid (UA) by differential pulse voltammetry employing the cationic surfactant, cetylpyridinium chloride. Differential pulse voltammetry measurements revealed that the cationic micellar media may separate the oxidation peak potentials of AA and UA present in the same solution by about 282 mV, which is enough to determine both species simultaneously. As in pH 7.0 the AA is more ionized than UA, its electrostatic attraction towards the cationic micelles formed onto the surface of glassy carbon electrode is higher, therefore, promoting a decrease in the overpotential and increasing the electron transfer rate. Calibration curves to AA and UA in the concentration range from 4.70 up to 220 µmol L-1 and 0.50 up to 110 µmol L-1 were built. The proposed methodology was applied for the simultaneous determination of AA and UA in human urine samples.
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spelling Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetryuric acidascorbic aciddifferential pulse voltammetrycationic surfactantmicellesThe present work describes an analytical methodology for simultaneous determination of ascorbic acid (AA) and uric acid (UA) by differential pulse voltammetry employing the cationic surfactant, cetylpyridinium chloride. Differential pulse voltammetry measurements revealed that the cationic micellar media may separate the oxidation peak potentials of AA and UA present in the same solution by about 282 mV, which is enough to determine both species simultaneously. As in pH 7.0 the AA is more ionized than UA, its electrostatic attraction towards the cationic micelles formed onto the surface of glassy carbon electrode is higher, therefore, promoting a decrease in the overpotential and increasing the electron transfer rate. Calibration curves to AA and UA in the concentration range from 4.70 up to 220 µmol L-1 and 0.50 up to 110 µmol L-1 were built. The proposed methodology was applied for the simultaneous determination of AA and UA in human urine samples.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000800017Journal of the Brazilian Chemical Society v.19 n.8 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000800017info:eu-repo/semantics/openAccessReis,Alaécio P. dosTarley,César R. T.Kubota,Lauro T.eng2008-12-09T00:00:00Zoai:scielo:S0103-50532008000800017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2008-12-09T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
title Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
spellingShingle Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
Reis,Alaécio P. dos
uric acid
ascorbic acid
differential pulse voltammetry
cationic surfactant
micelles
title_short Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
title_full Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
title_fullStr Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
title_full_unstemmed Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
title_sort Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
author Reis,Alaécio P. dos
author_facet Reis,Alaécio P. dos
Tarley,César R. T.
Kubota,Lauro T.
author_role author
author2 Tarley,César R. T.
Kubota,Lauro T.
author2_role author
author
dc.contributor.author.fl_str_mv Reis,Alaécio P. dos
Tarley,César R. T.
Kubota,Lauro T.
dc.subject.por.fl_str_mv uric acid
ascorbic acid
differential pulse voltammetry
cationic surfactant
micelles
topic uric acid
ascorbic acid
differential pulse voltammetry
cationic surfactant
micelles
description The present work describes an analytical methodology for simultaneous determination of ascorbic acid (AA) and uric acid (UA) by differential pulse voltammetry employing the cationic surfactant, cetylpyridinium chloride. Differential pulse voltammetry measurements revealed that the cationic micellar media may separate the oxidation peak potentials of AA and UA present in the same solution by about 282 mV, which is enough to determine both species simultaneously. As in pH 7.0 the AA is more ionized than UA, its electrostatic attraction towards the cationic micelles formed onto the surface of glassy carbon electrode is higher, therefore, promoting a decrease in the overpotential and increasing the electron transfer rate. Calibration curves to AA and UA in the concentration range from 4.70 up to 220 µmol L-1 and 0.50 up to 110 µmol L-1 were built. The proposed methodology was applied for the simultaneous determination of AA and UA in human urine samples.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
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=S0103-50532008000800017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000800017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532008000800017
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.19 n.8 2008
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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