Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s10008-015-3078-2 http://hdl.handle.net/11449/177599 |
Resumo: | Some diuretic substances are controlled and monitored by the World Anti-Doping Agency as prohibited substances for use by athletes, such as triamterene (TRT). Thus, this work describes a voltammetric method based on graphite-epoxy composite electrode modified by tosyl-functionalized magnetic particles (GECE/MPs-To) for determination of TRT diuretic in urine sample. The TRT presented an oxidation peak at +1.24 V at GECE/MPs-To with irreversible behavior. Controlled potential electrolysis of the TRT at +1.26 V indicated the two electrons are transferred during amine group oxidation and the main product was identified by LC-MS/MS. The anodic peak current is 25 % higher at the modified electrode, suggesting that TRT is adsorbed on the magnetic particles. Using optimized conditions by using multivariate optimization of the parameters inherent of the square wave voltammetry, a calibration curve was constructed with a linear relationship for TRT from 0.500 to 99.8 μmol L−1. The limits of detection and quantification were 1.47 and 4.91 × 10−7 mol L−1, respectively. The proposed method was applied to urine sample and validated by LC-MS/MS technique where the values found and compared between the two techniques showed no significant difference at 95 % confidence. |
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Repositório Institucional da UNESP |
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Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sampleDiureticGraphite-epoxy composite electrodeMagnetic particlesMultivariate optimizationTriamtereneVoltammetric sensorSome diuretic substances are controlled and monitored by the World Anti-Doping Agency as prohibited substances for use by athletes, such as triamterene (TRT). Thus, this work describes a voltammetric method based on graphite-epoxy composite electrode modified by tosyl-functionalized magnetic particles (GECE/MPs-To) for determination of TRT diuretic in urine sample. The TRT presented an oxidation peak at +1.24 V at GECE/MPs-To with irreversible behavior. Controlled potential electrolysis of the TRT at +1.26 V indicated the two electrons are transferred during amine group oxidation and the main product was identified by LC-MS/MS. The anodic peak current is 25 % higher at the modified electrode, suggesting that TRT is adsorbed on the magnetic particles. Using optimized conditions by using multivariate optimization of the parameters inherent of the square wave voltammetry, a calibration curve was constructed with a linear relationship for TRT from 0.500 to 99.8 μmol L−1. The limits of detection and quantification were 1.47 and 4.91 × 10−7 mol L−1, respectively. The proposed method was applied to urine sample and validated by LC-MS/MS technique where the values found and compared between the two techniques showed no significant difference at 95 % confidence.Departamento de Química UNESP Universidade Estadual Paulista Júlio Mesquita Filho Instituto de Química de Araraquara, Rua Francisco Degni, 55, Bairro Quitandinha,Departamento de Química Grupo de Sensor e Biosensor Universidade Autônoma de Barcelona, BellaterraDepartamento de Química UNESP Universidade Estadual Paulista Júlio Mesquita Filho Instituto de Química de Araraquara, Rua Francisco Degni, 55, Bairro Quitandinha,Universidade Estadual Paulista (Unesp)Universidade Autônoma de BarcelonaHudari, Felipe Fantinato [UNESP]da Silva, Bianca Ferreira [UNESP]Pividori, Maria IsabelZanoni, Maria Valnice Boldrin [UNESP]2018-12-11T17:26:16Z2018-12-11T17:26:16Z2016-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2491-2501application/pdfhttp://dx.doi.org/10.1007/s10008-015-3078-2Journal of Solid State Electrochemistry, v. 20, n. 9, p. 2491-2501, 2016.1432-8488http://hdl.handle.net/11449/17759910.1007/s10008-015-3078-22-s2.0-849474171252-s2.0-84947417125.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Solid State Electrochemistry0,661info:eu-repo/semantics/openAccess2023-10-27T06:10:48Zoai:repositorio.unesp.br:11449/177599Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:10:46.361181Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
title |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
spellingShingle |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample Hudari, Felipe Fantinato [UNESP] Diuretic Graphite-epoxy composite electrode Magnetic particles Multivariate optimization Triamterene Voltammetric sensor |
title_short |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
title_full |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
title_fullStr |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
title_full_unstemmed |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
title_sort |
Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample |
author |
Hudari, Felipe Fantinato [UNESP] |
author_facet |
Hudari, Felipe Fantinato [UNESP] da Silva, Bianca Ferreira [UNESP] Pividori, Maria Isabel Zanoni, Maria Valnice Boldrin [UNESP] |
author_role |
author |
author2 |
da Silva, Bianca Ferreira [UNESP] Pividori, Maria Isabel Zanoni, Maria Valnice Boldrin [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Autônoma de Barcelona |
dc.contributor.author.fl_str_mv |
Hudari, Felipe Fantinato [UNESP] da Silva, Bianca Ferreira [UNESP] Pividori, Maria Isabel Zanoni, Maria Valnice Boldrin [UNESP] |
dc.subject.por.fl_str_mv |
Diuretic Graphite-epoxy composite electrode Magnetic particles Multivariate optimization Triamterene Voltammetric sensor |
topic |
Diuretic Graphite-epoxy composite electrode Magnetic particles Multivariate optimization Triamterene Voltammetric sensor |
description |
Some diuretic substances are controlled and monitored by the World Anti-Doping Agency as prohibited substances for use by athletes, such as triamterene (TRT). Thus, this work describes a voltammetric method based on graphite-epoxy composite electrode modified by tosyl-functionalized magnetic particles (GECE/MPs-To) for determination of TRT diuretic in urine sample. The TRT presented an oxidation peak at +1.24 V at GECE/MPs-To with irreversible behavior. Controlled potential electrolysis of the TRT at +1.26 V indicated the two electrons are transferred during amine group oxidation and the main product was identified by LC-MS/MS. The anodic peak current is 25 % higher at the modified electrode, suggesting that TRT is adsorbed on the magnetic particles. Using optimized conditions by using multivariate optimization of the parameters inherent of the square wave voltammetry, a calibration curve was constructed with a linear relationship for TRT from 0.500 to 99.8 μmol L−1. The limits of detection and quantification were 1.47 and 4.91 × 10−7 mol L−1, respectively. The proposed method was applied to urine sample and validated by LC-MS/MS technique where the values found and compared between the two techniques showed no significant difference at 95 % confidence. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-09-01 2018-12-11T17:26:16Z 2018-12-11T17:26:16Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1007/s10008-015-3078-2 Journal of Solid State Electrochemistry, v. 20, n. 9, p. 2491-2501, 2016. 1432-8488 http://hdl.handle.net/11449/177599 10.1007/s10008-015-3078-2 2-s2.0-84947417125 2-s2.0-84947417125.pdf |
url |
http://dx.doi.org/10.1007/s10008-015-3078-2 http://hdl.handle.net/11449/177599 |
identifier_str_mv |
Journal of Solid State Electrochemistry, v. 20, n. 9, p. 2491-2501, 2016. 1432-8488 10.1007/s10008-015-3078-2 2-s2.0-84947417125 2-s2.0-84947417125.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Solid State Electrochemistry 0,661 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
2491-2501 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128614684688384 |