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A chemically modified carbon paste electrode (CPE), consisting of 2,2’-[ (1E)- (1,2- phenylenebis (azanylylidene)] bis (methanylylidene)]bis (benzene-1,4-diol) (PBD) and multiwalled carbon nano-tubes (CNTs), was used to study the electrocatalytic oxidation of dopamine using cyclic voltamme-try, chronoamperometry, and differential pulse voltammetry (DPV). First, the electrochemical be-havior of the modified electrode was investigated in buffer solution. Then the diffusion coefficient, electrocatalytic rate constant, and electron-transfer coefficient for dopamine oxidation at the sur-face of the PBD-modified CNT paste electrode were determined using electrochemical approaches. It was found that under optimum conditions (pH = 7.0), the oxidation of dopamine at the surface of such an electrode occurred at about 200 mV, lower than that of an unmodified CPE. DPV of dopa-mine at the modified electrode exhibited two linear dynamic ranges, with a detection limit of 1.0 μmol/L. Finally, DPV was used successfully for the simultaneous determination of dopamine, uric acid, and folic acid at the modified electrode, and detection limits of 1.0, 1.2, and 2.7 μmol/L were obtained for dopamine, uric acid, and folic acid, respectively. This method was also used for the determination of dopamine in a pharmaceutical preparation using the standard addition method.
A chemically modified carbon paste electrode (CPE) consisting of 2,2’- [(1E) - (1,2-phenylenebis (azanylylidene)] bis (methanylylidene)] bis and multiwalled carbon nano-tubes (CNTs), was used to study the electrocatalytic oxidation of dopamine using cyclic voltamme-try, chronoamperometry, and differential pulse voltammetry (DPV). First, the electrochemical be-havior of the modified electrode was investigated in buffer solution. Then the diffusion coefficient, electrocatalytic rate constant, and electron-transfer coefficient for dopamine oxidation at the sur-face of the PBD-modified CNT paste electrode were determined using electrochemical approaches. It was found that under optimum conditions (pH = 7.0) , the oxidation of dopamine at the surface of such an electrode occurred at about 200 mV, lower than that of an unmodified CPE. DPV of dopa-mine at the modified electrode showed two linear dynamic ranges with a detection limit of 1.0 μmol / L Finally, DPV was used successfully for the simultaneous determination of dopamine, uric acid, and folic acid at the modified electrode, and detection limits of 1.0, 1.2, and 2.7 μmol / L were obtained for dopamine, uric acid, and folic acid, respectively. also used for the determination of dopamine in a pharmaceutical preparation using the standard addition method.