Preparation and electrochemical application of rutin biosensor for differential pulse voltammetric determination of NADH in the presence of acetaminophen

被引:3
作者
Zare, Hamid R. [1 ]
Samimi, Reza [1 ]
Nasirizadeh, Navid [1 ]
Mazloum-Ardakani, Mohammad [1 ]
机构
[1] Yazd Univ, Dept Chem, Yazd 89195741, Iran
关键词
electrocatalytic behavior; rutin; NADH; biosensor; acetaminophen; GLASSY-CARBON ELECTRODE; NICOTINAMIDE ADENINE-DINUCLEOTIDE; CHEMICALLY-MODIFIED ELECTRODES; MICROBAND GOLD ELECTRODE; ELECTROCATALYTIC OXIDATION; CATALYTIC-OXIDATION; GRAPHITE-ELECTRODES; PASTE ELECTRODE; ASCORBIC-ACID; FILM;
D O I
10.2298/JSC100209111Z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrocatalytic behavior of reduced nicotinamide adenine dinucleotide (NADH) was studied at the surface of a rutin biosensor, using various electrochemical methods. According to the results, the rutin biosensor had a strongly electrocatalytic effect on the oxidation of NADH with the overpotential being decreased by about 450 mV as compared to the process at a bare glassy carbon electrode, GCE. This value is significantly greater than the value of 220 mV that was reported for rutin embedded in a lipid-cast film. The kinetic parameters of the electron transfer coefficient, alpha, and the heterogeneous charge transfer rate constant, k(h), for the electrocatalytic oxidation of NADH at the rutin biosensor were estimated. Furthermore, the linear dynamic range; sensitivity and limit of detection for NADH were evaluated using the differential pulse voltammetry method. The advantages of this biosensor for the determination of NADH are excellent catalytic activity and reproducibility, good detection limit and high exchange current density. The rutin biosensor could separate the oxidation peak potentials of NADH and acetaminophen present in the same solution while at a bare GCE, the peak potentials were indistinguishable.
引用
收藏
页码:1421 / 1434
页数:14
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