Electrochemical oxidation of mitoxantrone at a glassy carbon electrode

Bibliographic Details
Main Author: Brett, A. M. Oliveira
Publication Date: 1999
Other Authors: Macedo, T. R. A., Raimundo, D., Marques, M. H., Serrano, S. H. P.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10316/5269
https://doi.org/10.1007/BF01206688
Summary: Mitoxantrone is an anthracycline used as an antitumour antibiotic for leukaemia and breast cancer treatment, due to its interaction with DNA. However, the molecular mechanism of the antitumour action is not completely understood. Using a glassy carbon electrode the electrochemical oxidation of mitoxantrone was shown to be a complex, pH-dependent, irreversible electrode process involving several metabolites. Comparison of the electrochemical oxidation behaviour of mitoxantrone, ametantrone and aminantrone enabled a deeper understanding of the mechanism and showed the relevance of electrochemical data for the understanding of the cytotoxicity of mitoxantrone. Since mitoxantrone and its oxidation products adsorb strongly on the electrode surface, causing severe problems of electrode fouling, reproducible electroanalytical determinations could only be done at very low concentrations and in an aqueous buffer supporting electrolyte containing 30% ethanol. The detection limit obtained was 10-7 M.
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spelling Electrochemical oxidation of mitoxantrone at a glassy carbon electrodeBioelectrochemistryMitoxantrone oxidationVoltammetryMitoxantrone is an anthracycline used as an antitumour antibiotic for leukaemia and breast cancer treatment, due to its interaction with DNA. However, the molecular mechanism of the antitumour action is not completely understood. Using a glassy carbon electrode the electrochemical oxidation of mitoxantrone was shown to be a complex, pH-dependent, irreversible electrode process involving several metabolites. Comparison of the electrochemical oxidation behaviour of mitoxantrone, ametantrone and aminantrone enabled a deeper understanding of the mechanism and showed the relevance of electrochemical data for the understanding of the cytotoxicity of mitoxantrone. Since mitoxantrone and its oxidation products adsorb strongly on the electrode surface, causing severe problems of electrode fouling, reproducible electroanalytical determinations could only be done at very low concentrations and in an aqueous buffer supporting electrolyte containing 30% ethanol. The detection limit obtained was 10-7 M.http://www.sciencedirect.com/science/article/B6TF4-3W3N6Y2-1J/1/5ffa47da56de732d1903bdf9a6c163c91999info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttps://hdl.handle.net/10316/5269https://hdl.handle.net/10316/5269https://doi.org/10.1007/BF01206688engAnalytica Chimica Acta. 385:1-3 (1999) 401-408Brett, A. M. OliveiraMacedo, T. R. A.Raimundo, D.Marques, M. H.Serrano, S. H. P.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2021-09-22T09:26:24Zoai:estudogeral.uc.pt:10316/5269Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:24:16.512199Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
title Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
spellingShingle Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
Brett, A. M. Oliveira
Bioelectrochemistry
Mitoxantrone oxidation
Voltammetry
title_short Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
title_full Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
title_fullStr Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
title_full_unstemmed Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
title_sort Electrochemical oxidation of mitoxantrone at a glassy carbon electrode
author Brett, A. M. Oliveira
author_facet Brett, A. M. Oliveira
Macedo, T. R. A.
Raimundo, D.
Marques, M. H.
Serrano, S. H. P.
author_role author
author2 Macedo, T. R. A.
Raimundo, D.
Marques, M. H.
Serrano, S. H. P.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Brett, A. M. Oliveira
Macedo, T. R. A.
Raimundo, D.
Marques, M. H.
Serrano, S. H. P.
dc.subject.por.fl_str_mv Bioelectrochemistry
Mitoxantrone oxidation
Voltammetry
topic Bioelectrochemistry
Mitoxantrone oxidation
Voltammetry
description Mitoxantrone is an anthracycline used as an antitumour antibiotic for leukaemia and breast cancer treatment, due to its interaction with DNA. However, the molecular mechanism of the antitumour action is not completely understood. Using a glassy carbon electrode the electrochemical oxidation of mitoxantrone was shown to be a complex, pH-dependent, irreversible electrode process involving several metabolites. Comparison of the electrochemical oxidation behaviour of mitoxantrone, ametantrone and aminantrone enabled a deeper understanding of the mechanism and showed the relevance of electrochemical data for the understanding of the cytotoxicity of mitoxantrone. Since mitoxantrone and its oxidation products adsorb strongly on the electrode surface, causing severe problems of electrode fouling, reproducible electroanalytical determinations could only be done at very low concentrations and in an aqueous buffer supporting electrolyte containing 30% ethanol. The detection limit obtained was 10-7 M.
publishDate 1999
dc.date.none.fl_str_mv 1999
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10316/5269
https://hdl.handle.net/10316/5269
https://doi.org/10.1007/BF01206688
url https://hdl.handle.net/10316/5269
https://doi.org/10.1007/BF01206688
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Analytica Chimica Acta. 385:1-3 (1999) 401-408
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dc.format.none.fl_str_mv aplication/PDF
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