Study of the electrochemical reduction of amoebicide Teclozan and its amperometric determination in pharmaceutical formulations
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , |
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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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:29462024-08-05T22:39:13.170221Repositório 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 |
|
_version_ |
1808129447289683968 |