Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations

Detalhes bibliográficos
Autor(a) principal: Santos, Andri L.
Data de Publicação: 2008
Outros Autores: Takeuchi, Regina M. [UNESP], Stradiotto, Nelson Ramos [UNESP], Esteves, Ana Paula, Medeiros, Maria Jose
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0103-50532008000600014
http://hdl.handle.net/11449/25820
Resumo: The electrochemical reduction of amoebicide Teclozan (TEC) was studied on a glassy carbon electrode in acetonitrile. Controlled-potential electrolyses were performed for coulometric and preparative purposes. The electrogenerated products were isolated by liquid-liquid extraction and characterized by (1)H NMR. It was observed that TEC presents two voltammetric peaks, each one associated with the cleavage of two C-Cl bonds. In presence of a proton donor it was observed that the first peak at -1.8 V promotes mainly the reduction of the groups CHCl(2) to CH(2)Cl and the second one at -2.2 V promotes the reduction of the groups CH(2)Cl to CH(3) giving as the sole product the completely dechlorinated TEC derivative with yields between 82 and 97%. In addition, a comparative study between the analytical performance of voltammetric techniques and amperometric detection of TEC in hydrodynamic conditions was performed. The amperometric detection was more sensitive than all evaluated voltammetric techniques, providing a detection limit of 8.9 x 10(-6) mol L(-1).
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spelling Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulationsamperometric detectionglassy carbon electrodechloroacetamidesTeclozanThe electrochemical reduction of amoebicide Teclozan (TEC) was studied on a glassy carbon electrode in acetonitrile. Controlled-potential electrolyses were performed for coulometric and preparative purposes. The electrogenerated products were isolated by liquid-liquid extraction and characterized by (1)H NMR. It was observed that TEC presents two voltammetric peaks, each one associated with the cleavage of two C-Cl bonds. In presence of a proton donor it was observed that the first peak at -1.8 V promotes mainly the reduction of the groups CHCl(2) to CH(2)Cl and the second one at -2.2 V promotes the reduction of the groups CH(2)Cl to CH(3) giving as the sole product the completely dechlorinated TEC derivative with yields between 82 and 97%. In addition, a comparative study between the analytical performance of voltammetric techniques and amperometric detection of TEC in hydrodynamic conditions was performed. The amperometric detection was more sensitive than all evaluated voltammetric techniques, providing a detection limit of 8.9 x 10(-6) mol L(-1).Minho University, PortugalCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sanofi-Synthelabo Brazil LtdaUniversidade Federal de Uberlândia (UFU), Fac Ciencias Integradas Pontal, BR-38302000 Ituiutaba, MG, BrazilUniv Estadual Paulista, BR-14801970 Araraquara, SP, BrazilUniv Minho, Ctr Quim, P-4704553 Braga, PortugalUniv Estadual Paulista, BR-14801970 Araraquara, SP, BrazilCAPES: 1088068CAPES: 1087061FAPESP: 03/05567-7FAPESP: 03/09334-7Soc Brasileira QuimicaUniversidade Federal de Uberlândia (UFU)Universidade Estadual Paulista (Unesp)Univ MinhoSantos, Andri L.Takeuchi, Regina M. [UNESP]Stradiotto, Nelson Ramos [UNESP]Esteves, Ana PaulaMedeiros, Maria Jose2014-05-20T14:19:17Z2014-05-20T14:19:17Z2008-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1144-1152http://dx.doi.org/10.1590/S0103-50532008000600014Journal of The Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 19, n. 6, p. 1144-1152, 2008.0103-5053http://hdl.handle.net/11449/2582010.1590/S0103-50532008000600014S0103-50532008000600014WOS:000259121600014S0103-50532008000600014.pdf0072173018005712Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,357info:eu-repo/semantics/openAccess2021-10-23T17:45:47Zoai:repositorio.unesp.br:11449/25820Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T17:45:47Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
title Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
spellingShingle Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
Santos, Andri L.
amperometric detection
glassy carbon electrode
chloroacetamides
Teclozan
title_short Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
title_full Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
title_fullStr Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
title_full_unstemmed Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
title_sort Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
author Santos, Andri L.
author_facet Santos, Andri L.
Takeuchi, Regina M. [UNESP]
Stradiotto, Nelson Ramos [UNESP]
Esteves, Ana Paula
Medeiros, Maria Jose
author_role author
author2 Takeuchi, Regina M. [UNESP]
Stradiotto, Nelson Ramos [UNESP]
Esteves, Ana Paula
Medeiros, Maria Jose
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Uberlândia (UFU)
Universidade Estadual Paulista (Unesp)
Univ Minho
dc.contributor.author.fl_str_mv Santos, Andri L.
Takeuchi, Regina M. [UNESP]
Stradiotto, Nelson Ramos [UNESP]
Esteves, Ana Paula
Medeiros, Maria Jose
dc.subject.por.fl_str_mv amperometric detection
glassy carbon electrode
chloroacetamides
Teclozan
topic amperometric detection
glassy carbon electrode
chloroacetamides
Teclozan
description The electrochemical reduction of amoebicide Teclozan (TEC) was studied on a glassy carbon electrode in acetonitrile. Controlled-potential electrolyses were performed for coulometric and preparative purposes. The electrogenerated products were isolated by liquid-liquid extraction and characterized by (1)H NMR. It was observed that TEC presents two voltammetric peaks, each one associated with the cleavage of two C-Cl bonds. In presence of a proton donor it was observed that the first peak at -1.8 V promotes mainly the reduction of the groups CHCl(2) to CH(2)Cl and the second one at -2.2 V promotes the reduction of the groups CH(2)Cl to CH(3) giving as the sole product the completely dechlorinated TEC derivative with yields between 82 and 97%. In addition, a comparative study between the analytical performance of voltammetric techniques and amperometric detection of TEC in hydrodynamic conditions was performed. The amperometric detection was more sensitive than all evaluated voltammetric techniques, providing a detection limit of 8.9 x 10(-6) mol L(-1).
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
2014-05-20T14:19:17Z
2014-05-20T14:19:17Z
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/10.1590/S0103-50532008000600014
Journal of The Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 19, n. 6, p. 1144-1152, 2008.
0103-5053
http://hdl.handle.net/11449/25820
10.1590/S0103-50532008000600014
S0103-50532008000600014
WOS:000259121600014
S0103-50532008000600014.pdf
0072173018005712
url http://dx.doi.org/10.1590/S0103-50532008000600014
http://hdl.handle.net/11449/25820
identifier_str_mv Journal of The Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 19, n. 6, p. 1144-1152, 2008.
0103-5053
10.1590/S0103-50532008000600014
S0103-50532008000600014
WOS:000259121600014
S0103-50532008000600014.pdf
0072173018005712
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
1.444
0,357
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1144-1152
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
dc.source.none.fl_str_mv Web of Science
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
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