Differential pulse voltammetric enzyme-linked immunoassay for the determination of Helicobacter pylori specific immunoglobulin G (IgG) antibody

A differential pulse voltammetric enzyme-linked immunoassay for the determination of helicobacter pylori ( H. pylori) specific IgG antibody in human serum has been developed. The method is based on coupling the oxidation reaction of 3,3′,5,5′-tetramethylbenzidine (TMB)-H 2O 2 that is catalysed by horseradish peroxidase-IgG(HRP-IgG) conjugate with the electro-reduction of the enzymatic product to measure the activity of HRP-IgG. The latter reaction exhibits a sensitive differential pulse voltammetric response at 0.1 V (versus Ag AgCl ) in pH 4.0 acetate buffer solution. So, the H. pylori specific IgG antibody could be detected. The detection limit of present method for H. pylori specific IgG antibody was 1.0 units ml −1, which was about seven times lower than that obtained by traditional spectrophotometric ELISA procedure.