Electrocatalytic oxidation of the reduced nicotinamide adenine dinucleotide at carbon ionic liquid electrode modified with polythionine/multi-walled carbon nanotubes composite
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作者:
Nannan Mai
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Nannan Mai
Xiaoying Liu
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Xiaoying Liu
Xiandong Zeng
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Xiandong Zeng
Liang Xing
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Liang Xing
Wanzhi Wei
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Wanzhi Wei
Shenglian Luo
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机构:Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
Shenglian Luo
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[1] Hunan University,State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering
A carbon ionic liquid electrode (CILE) was modified with a polythionine (PTh)/multi-walled carbon nanotubes (MWCNTs) composite and used for the detection of reduced nicotinamide adenine dinucleotide (NADH). The electrode was prepared by electrochemical polymerization of thionine on the MWCNTs in neutral medium. Cyclic voltammetry indicated that the electrode was capable of mediating the oxidation of NADH at an overpotential as low as 0.03 V. Amperometric experiments showed that a sensitive and stable response towards NADH is obtained within 5 s. The linear range for the determination of NADH is from 0.8 μmol L−1 to 422 μmol L−1, with a detection limit of 0.26 μmol L−1 (S/N = 3). The wide linear range, lower detection limit and faster response towards NADH suggests that the new method potentially is useful for developing NAD+-dependent enzyme-based biosensors.