Issue 11, 2011

Multi-wall carbon nanotubes as a sensor and ferrocene dicarboxylic acid as a mediator for voltammetric determination of glutathione in hemolysed erythrocyte

Abstract

A sensitive and selective electrochemical method was developed for determination of glutathione (GSH) in hemolysed erythrocyte using a ferrocene dicarboxylic acid modified carbon nanotubes paste electrode (FDCCNTPE). Cyclic voltammetry (CV), double potential-step chronoamperometry and differential pulse voltammetric (DPV) were used to investigate the suitability of ferrocene dicarboxylic acid at the surface of a multi-wall carbon nanotubes paste electrode as a mediator for the electrocatalytic oxidation of glutathione in aqueous solutions with various pH. The results showed that FDCCNTPE had high electrocatalytic activity for the electrooxidation of glutathione. Under optimum conditions (pH 7.00), oxidation of GSH occurs at a potential about 230 mV less positive than that at the unmodified carbon nanotubes paste electrode. The catalytic reaction rate constant, kh was calculated (1.98 × 104 M−1 s−1) using chronoamperometry. The electrocatalytic oxidation peak current of GSH showed two linear dynamic ranges with a detection limit of 0.2 μmol L−1 GSH. The linear calibration ranges were obtained between 0.5–24 μmol L−1 and 24–122 μmol L−1 GSH using the DPV method. Finally, the proposed method was also examined as a selective, simple and precise electrochemical sensor for the determination of GSH in real samples such as hemolysed erythrocyte.

Graphical abstract: Multi-wall carbon nanotubes as a sensor and ferrocene dicarboxylic acid as a mediator for voltammetric determination of glutathione in hemolysed erythrocyte

Article information

Article type
Paper
Submitted
19 Jan 2011
Accepted
12 Sep 2011
First published
18 Oct 2011

Anal. Methods, 2011,3, 2637-2643

Multi-wall carbon nanotubes as a sensor and ferrocene dicarboxylic acid as a mediator for voltammetric determination of glutathione in hemolysed erythrocyte

J. B. Raoof, R. Ojani, H. Karimi-Maleh, M. R. Hajmohamadi and P. Biparva, Anal. Methods, 2011, 3, 2637 DOI: 10.1039/C1AY05031A

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