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Electrochemical Behaviour of Copper Nitroprusside Generated in situ Onto the Graphite Paste Electrode Surface, and its Application in the Determination of N-Acethylcysteine

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Resumo:Copper nitroprusside (CuNP) was generated on the graphite paste electrode using a new methodology of the preparation. The electrochemical studies were carried out by cyclic voltammetry technique. The cyclic voltammogram of the modified electrode, CuNP showed two redox couples (E0’)1=0.22 and (E0’)2=0.88 V vs. SCE attributed to Cu(I)/Cu(II) and Fe(II)(CN)5NO/Fe(III)(CN)5NO, respectively. The nature of the cation affect the (E0’)1 and (E0’)2, as current intensity, shifting the E0’ for more positive potentials, for two redox processes. The voltammograms obtained with different KCl concentrations (0.1-3.0 mol L-1) exhibit a shift in the (E0’)1 to more positive potentials; this change was linear with the supporting electrolyte concentrations change. It was verified that the (E0’)1 remained practically constant at pH between 6 and 3. However, a new process with (E0’)3 (0.48 V) appears at pH<3 and it was ascribed to formation of intermediary species. The redox couple at (E0’)2=0.88 V presents an electrocatalytic response for N-acethylcysteine. The modified graphite paste electrode gives a linear response between 5.0´10-4 to 1.0´10-2 mol L-1 of N-acethylcysteine with a detection limit of 4.5´10-4 (±5%) mol L-1 (n=3) and an amperometric sensitivity of 4.9 mA/mmol L-1. The electrocatalytic oxidation of N-acethylcysteine compounds by the mediator has been used for the determination of N-acethylcysteine in a commercially pharmaceutical available product.
Autores principais:Carmo,D. Ribeiro do
Outros Autores:Silva,R. Moutinho da; Stradiotto,N. Ramos
Assunto:copper nitroprusside modified electrode electrocatalysis N- acethylcysteine oxidation
Ano:2005
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:português
Origem:SciELO Portugal
Descrição
Resumo:Copper nitroprusside (CuNP) was generated on the graphite paste electrode using a new methodology of the preparation. The electrochemical studies were carried out by cyclic voltammetry technique. The cyclic voltammogram of the modified electrode, CuNP showed two redox couples (E0’)1=0.22 and (E0’)2=0.88 V vs. SCE attributed to Cu(I)/Cu(II) and Fe(II)(CN)5NO/Fe(III)(CN)5NO, respectively. The nature of the cation affect the (E0’)1 and (E0’)2, as current intensity, shifting the E0’ for more positive potentials, for two redox processes. The voltammograms obtained with different KCl concentrations (0.1-3.0 mol L-1) exhibit a shift in the (E0’)1 to more positive potentials; this change was linear with the supporting electrolyte concentrations change. It was verified that the (E0’)1 remained practically constant at pH between 6 and 3. However, a new process with (E0’)3 (0.48 V) appears at pH<3 and it was ascribed to formation of intermediary species. The redox couple at (E0’)2=0.88 V presents an electrocatalytic response for N-acethylcysteine. The modified graphite paste electrode gives a linear response between 5.0´10-4 to 1.0´10-2 mol L-1 of N-acethylcysteine with a detection limit of 4.5´10-4 (±5%) mol L-1 (n=3) and an amperometric sensitivity of 4.9 mA/mmol L-1. The electrocatalytic oxidation of N-acethylcysteine compounds by the mediator has been used for the determination of N-acethylcysteine in a commercially pharmaceutical available product.