A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide

Detalhes bibliográficos
Autor(a) principal: Semaan, Felipe S.
Data de Publicação: 2008
Outros Autores: Pinto, Edilson M., Cavalheiro, Éder T. G., Brett, Christopher M. A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8249
https://doi.org/10.1002/elan.200804329
Resumo: A graphite-polyurethane composite electrode has been used for the determination of furosemide, a antihypertensive drug, in pharmaceutical samples by anodic oxidation. Cyclic voltammetry and electrochemical impedance spectroscopy were used to characterize the electrooxidation process at +1.0 V vs. SCE over a wide pH range, with the result that no adsorption of analyte or products occurs, unlike at other carbon-based electrode materials. Quantification was carried out using cyclic voltammetry, differential pulse voltammetry, and square-wave voltammetry. Linear ranges were determined (up to 21 mumol L-1 with cyclic voltammetry) as well as limits of detection (0.15 mumol L-1 by differential pulse voltammetry). Four different types of commercial samples were successfully analyzed. Recovery tests were performed which agreed with those obtained by spectrophotometric evaluation. The advantages of this electrode material for repetitive analyzes, due to the fact that no electrode surface renewal is needed owing to the lack of adsorption, are highlighted.
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spelling A Graphite-Polyurethane Composite Electrode for the Analysis of FurosemideA graphite-polyurethane composite electrode has been used for the determination of furosemide, a antihypertensive drug, in pharmaceutical samples by anodic oxidation. Cyclic voltammetry and electrochemical impedance spectroscopy were used to characterize the electrooxidation process at +1.0 V vs. SCE over a wide pH range, with the result that no adsorption of analyte or products occurs, unlike at other carbon-based electrode materials. Quantification was carried out using cyclic voltammetry, differential pulse voltammetry, and square-wave voltammetry. Linear ranges were determined (up to 21 mumol L-1 with cyclic voltammetry) as well as limits of detection (0.15 mumol L-1 by differential pulse voltammetry). Four different types of commercial samples were successfully analyzed. Recovery tests were performed which agreed with those obtained by spectrophotometric evaluation. The advantages of this electrode material for repetitive analyzes, due to the fact that no electrode surface renewal is needed owing to the lack of adsorption, are highlighted.2008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8249http://hdl.handle.net/10316/8249https://doi.org/10.1002/elan.200804329engElectroanalysis. 20:21 (2008) 2287-2293Semaan, Felipe S.Pinto, Edilson M.Cavalheiro, Éder T. G.Brett, Christopher M. A.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-10-12T11:21:32Zoai:estudogeral.uc.pt:10316/8249Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:40.305677Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
title A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
spellingShingle A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
Semaan, Felipe S.
title_short A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
title_full A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
title_fullStr A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
title_full_unstemmed A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
title_sort A Graphite-Polyurethane Composite Electrode for the Analysis of Furosemide
author Semaan, Felipe S.
author_facet Semaan, Felipe S.
Pinto, Edilson M.
Cavalheiro, Éder T. G.
Brett, Christopher M. A.
author_role author
author2 Pinto, Edilson M.
Cavalheiro, Éder T. G.
Brett, Christopher M. A.
author2_role author
author
author
dc.contributor.author.fl_str_mv Semaan, Felipe S.
Pinto, Edilson M.
Cavalheiro, Éder T. G.
Brett, Christopher M. A.
description A graphite-polyurethane composite electrode has been used for the determination of furosemide, a antihypertensive drug, in pharmaceutical samples by anodic oxidation. Cyclic voltammetry and electrochemical impedance spectroscopy were used to characterize the electrooxidation process at +1.0 V vs. SCE over a wide pH range, with the result that no adsorption of analyte or products occurs, unlike at other carbon-based electrode materials. Quantification was carried out using cyclic voltammetry, differential pulse voltammetry, and square-wave voltammetry. Linear ranges were determined (up to 21 mumol L-1 with cyclic voltammetry) as well as limits of detection (0.15 mumol L-1 by differential pulse voltammetry). Four different types of commercial samples were successfully analyzed. Recovery tests were performed which agreed with those obtained by spectrophotometric evaluation. The advantages of this electrode material for repetitive analyzes, due to the fact that no electrode surface renewal is needed owing to the lack of adsorption, are highlighted.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8249
http://hdl.handle.net/10316/8249
https://doi.org/10.1002/elan.200804329
url http://hdl.handle.net/10316/8249
https://doi.org/10.1002/elan.200804329
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Electroanalysis. 20:21 (2008) 2287-2293
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