Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/27472
Title: Temozolomide chemical degradation to 5-aminoimidazole-4-carboxamide – Electrochemical study
Authors: Lopes, Ilanna C. 
Oliveira, Severino Carlos B. de 
Brett, Ana Maria Oliveira 
Keywords: Temozolomide chemical degradation; 5-Aminoimidazole-4-carboxamide; pH effect; Carbon electrode; Redox mechanism
Issue Date: 1-Sep-2013
Publisher: Elsevier
Citation: LOPES, Ilanna C.; OLIVEIRA, Severino Carlos B. de; OLIVEIRA-BRETT, Ana Maria - Temozolomide chemical degradation to 5-aminoimidazole-4-carboxamide – Electrochemical study. "Journal of Electroanalytical Chemistry". ISSN 1572-6657. Vol. 704 (2013) p. 183-189
Serial title, monograph or event: Journal of Electroanalytical Chemistry
Volume: 704
Abstract: The evaluation of the chemical degradation of temozolomide (TMZ), a potential anti-cancer drug, to its major metabolite 5-aminoimidazole-4-carboxamide (AIC), in aqueous solution with different pH values, was investigated at a glassy carbon electrode using cyclic and differential pulse voltammetry, and UV–Vis spectrophotometry. TMZ was incubated in aqueous solution, for different periods of time, and the changes in TMZ electrochemistry behaviour detected. The TMZ reduction is a pH-dependent irreversible process on the tetrazinone ring causing its irreversible breakdown. TMZ oxidation is a pH-dependent irreversible process that occurs in two consecutive charge transfer reactions. TMZ chemical degradation was electrochemically detected by the increase of the TMZ anodic peak current and the disappearance of the TMZ cathodic peak. The rate of chemical degradation increases with increasing pH and the mechanism corresponds to TMZ chemical degradation to AIC. The electrochemical behaviour of AIC over a wide pH range, was also investigated using cyclic, differential pulse and square wave voltammetry, AIC oxidation is an irreversible, diffusion-controlled process, pH-dependent up to a pH close to the pKa, and occurs in two consecutive charge transfer reactions, with the formation of two reversible redox products. A mechanism for AIC oxidation is proposed.
URI: http://hdl.handle.net/10316/27472
ISSN: 1572-6657
DOI: 10.1016/j.jelechem.2013.07.011
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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