Micelle-mediated method for simultaneous determination of ascorbic acid and uric acid by differential pulse voltammetry
Autor(a) principal: | |
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Data de Publicação: | 2008 |
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=S0103-50532008000800017 |
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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Journal of the Brazilian Chemical Society (Online) |
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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 |
_version_ |
1750318169400016896 |