Voltammetric Behaviour of Metronidazole at Mercury Electrodes

Detalhes bibliográficos
Autor(a) principal: La-Scalea,Mauro A.
Data de Publicação: 1999
Outros Autores: Serrano,Silvia H.P., Gutz,Ivano G.R.
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=S0103-50531999000200010
Resumo: Metronidazole is the most important drug of the group of 5-nitroimidazoles and possesses toxicity to anaerobic micro-organisms DNA being the main target for their biological action. The mechanism of biological action of metronidazole is dependent upon the nitro group reduction process. The reduction of metronidazole is pH dependent in acid medium and four electrons are involved in the complete reduction to the hydroxylamine derivative. In aprotic medium the reduction of the metronidazole occurs in two steps, the first involving one electron to form the nitro radical and the second step involving three more electrons until the formation of the hydroxylamine derivative. In this paper the mechanism of reduction of metronidazole was studied by using the voltammetric techniques: d.c. polarography, differential pulse polarography and cyclic voltammetry using the mercury drop as the working electrode.
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spelling Voltammetric Behaviour of Metronidazole at Mercury Electrodesmetronidazolenitro radicalvoltammetrypolarographyMetronidazole is the most important drug of the group of 5-nitroimidazoles and possesses toxicity to anaerobic micro-organisms DNA being the main target for their biological action. The mechanism of biological action of metronidazole is dependent upon the nitro group reduction process. The reduction of metronidazole is pH dependent in acid medium and four electrons are involved in the complete reduction to the hydroxylamine derivative. In aprotic medium the reduction of the metronidazole occurs in two steps, the first involving one electron to form the nitro radical and the second step involving three more electrons until the formation of the hydroxylamine derivative. In this paper the mechanism of reduction of metronidazole was studied by using the voltammetric techniques: d.c. polarography, differential pulse polarography and cyclic voltammetry using the mercury drop as the working electrode.Sociedade Brasileira de Química1999-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531999000200010Journal of the Brazilian Chemical Society v.10 n.2 1999reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50531999000200010info:eu-repo/semantics/openAccessLa-Scalea,Mauro A.Serrano,Silvia H.P.Gutz,Ivano G.R.eng2002-10-23T00:00:00Zoai:scielo:S0103-50531999000200010Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2002-10-23T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Voltammetric Behaviour of Metronidazole at Mercury Electrodes
title Voltammetric Behaviour of Metronidazole at Mercury Electrodes
spellingShingle Voltammetric Behaviour of Metronidazole at Mercury Electrodes
La-Scalea,Mauro A.
metronidazole
nitro radical
voltammetry
polarography
title_short Voltammetric Behaviour of Metronidazole at Mercury Electrodes
title_full Voltammetric Behaviour of Metronidazole at Mercury Electrodes
title_fullStr Voltammetric Behaviour of Metronidazole at Mercury Electrodes
title_full_unstemmed Voltammetric Behaviour of Metronidazole at Mercury Electrodes
title_sort Voltammetric Behaviour of Metronidazole at Mercury Electrodes
author La-Scalea,Mauro A.
author_facet La-Scalea,Mauro A.
Serrano,Silvia H.P.
Gutz,Ivano G.R.
author_role author
author2 Serrano,Silvia H.P.
Gutz,Ivano G.R.
author2_role author
author
dc.contributor.author.fl_str_mv La-Scalea,Mauro A.
Serrano,Silvia H.P.
Gutz,Ivano G.R.
dc.subject.por.fl_str_mv metronidazole
nitro radical
voltammetry
polarography
topic metronidazole
nitro radical
voltammetry
polarography
description Metronidazole is the most important drug of the group of 5-nitroimidazoles and possesses toxicity to anaerobic micro-organisms DNA being the main target for their biological action. The mechanism of biological action of metronidazole is dependent upon the nitro group reduction process. The reduction of metronidazole is pH dependent in acid medium and four electrons are involved in the complete reduction to the hydroxylamine derivative. In aprotic medium the reduction of the metronidazole occurs in two steps, the first involving one electron to form the nitro radical and the second step involving three more electrons until the formation of the hydroxylamine derivative. In this paper the mechanism of reduction of metronidazole was studied by using the voltammetric techniques: d.c. polarography, differential pulse polarography and cyclic voltammetry using the mercury drop as the working electrode.
publishDate 1999
dc.date.none.fl_str_mv 1999-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531999000200010
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50531999000200010
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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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.10 n.2 1999
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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instname_str Sociedade Brasileira de Química (SBQ)
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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
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