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In this study, Mn(Ⅱ) as a mimetic enzyme of horseradish peroxidase (HRP) was applied to the determination of hydrogen peroxide (H2O2). The method introduced in this paper is based on Mn(Ⅱ)’s catalytic effect on the oxidation of 4-aminoantipyrine(4-AAP) with modified Trinder’s reagent N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3, 5-dimethoxyaniline(DAOS) by H2O2. By coupling this mimetic catalytic reaction with the catalytic reaction of glucose oxidase (GOD), glucose can be detected. Under optimum conditions, the calibration graphs for the determination of H2O2 and glucose are in the range of 1.0×10-3?1.0×10-1 mol/L and 1.0×10-3?14×10-3 mol/L respectively. The detection limit is 5.9×10-4 mol/L for H2O2 and is 9.2×10-4 mol/L for glucose. The feasibility of Mn ( II ) as a HRP mimetic enzyme in practical clinical analysis has been proven in the determination of glucose in human serum. So far, Mn ( II ) is the simplest and the most inexpensive mimetic enzyme.
In this study, Mn (Ⅱ) as a mimetic enzyme of horseradish peroxidase (HRP) was applied to the determination of hydrogen peroxide (H2O2). The method introduced in this paper is based on Mn (Ⅱ) ’s catalytic effect on the oxidation of 4-aminoantipyrine (4-AAP) with modified Trinder’s reagent N-ethyl-N- (2-hydroxy-3- sulfopropyl) -3 by 5-dimethoxyaniline (DAOS) by H2O2. By coupling this mimetic catalytic reaction with the catalytic reaction of glucose oxidase (GOD), glucose can detected. Under optimum conditions, the calibration graphs for the determination of H2O2 and glucose are in the range of 1.0 × 10-3 · 1.0 × 10-1 mol / L and 1.0 × 10- The detection limit is 5.9 × 10-4 mol / L for H2O2 and 9.2 × 10-4 mol / L for glucose. The feasibility of Mn (II) as a HRP mimetic enzyme in practical clinical analysis has been proven in the determination of glucose in human serum. So far, Mn (II) is the simplest and the most inexpensive mimetic enzyme.