Poly-phenothiazine derivative-modified glassy carbon electrode for NADH electrocatalytic oxidation

被引:54
作者
Gligor, Delia [2 ]
Dilgin, Yusuf [3 ]
Popescu, Ionel Catalin [2 ]
Gorton, Lo [1 ]
机构
[1] Lund Univ, Dept Analyt Chem, SE-22100 Lund, Sweden
[2] Univ Babes Bolyai, Dept Phys Chem, Cluj Napoca 400028, Romania
[3] Canakkale Onsekiz Mart Univ, Sci & Arts Fac, Dept Chem, TR-17020 Canakkale, Turkey
基金
瑞典研究理事会;
关键词
NADH electrocatalytic oxidation; Poly(phenothiazine derivative); Electropolymerization; NICOTINAMIDE ADENINE-DINUCLEOTIDE; ELECTROPOLYMERIZED FILMS; AMPEROMETRIC BIOSENSORS; POLY(ANILINE)-COATED ELECTRODES; PART II; DEHYDROGENASE; 3,4-DIHYDROXYBENZALDEHYDE; ELECTROOXIDATION; MEDIATORS; COENZYMES;
D O I
10.1016/j.electacta.2008.11.053
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electropolymerization of a new phenothiazine derivative (bis-phenothiazin-3-yl methane; BPhM) on glassy carbon (GC) electrode generates a conducting film of poly-BPhM. in stable contact with the electrode surface. The heterogeneous electron-transfer process corresponding to the modified electrode is characterized by a high rate constant (50.4 s(-1), pH 7). The CC/poly-BPhM electrode shows excellent electrocatalytic activity toward NADH oxidation. The rate constant for catalytic NADH oxidation, estimated from rotating disk electrode (RDE) measurements and extrapolated to zero concentration of NADH, was found to be 9.4 x 10(4) M-1 s(-1) (pH 7). The amperometric detection of NADH, at +200 mV vs. SCE, is described by the following electroanalytical parameters: a sensitivity of 1.82 mA M-1, a detection limit of 2 mu M and a linear domain up to 0.1 mM NADH. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3124 / 3128
页数:5
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