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咖啡酸玻碳修饰电极对烟酰胺腺嘌呤二核苷酸的电催化氧化 被引量:5

Electrocatalytic Oxidation of Dihydronicotinamide Adenine Dinucleotide at Caffeic Acid Glassy Carbon Modified Electrodes
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摘要 研究了咖啡酸修饰电极的制备、性质及对NADH的电催化作用。修饰电极在 0 .1mol/LPBS缓冲溶液中 (pH 7.0 )于 0 .0~ +0 .5 0V(vs.Ag/AgCl )电位范围内呈现一对氧化还原峰 ,式量电位 (E0′)为 +0 .2 5 0V(vs.Ag/AgCl)。E0′随pH增加而朝负方向移动 ,pH在 5 .0~ 8.0范围内 ,其线性回归方程为E0′=0 .6 2 33-0 0 5 996pH ,R =0 .996 9。表观电极反应速率常数 (Ks)为 12 .3s-1。电极反应的电子数为 2且有 2个质子参与。该修饰电极对NADH的氧化具有很好的电催化作用。NADH浓度在 0 .1~ 6 .0mmol/L范围内与峰电流呈现良好的线性关系。 The preparation and electrochemical properties of caffeic acid modified glassy carbon electrode and the electrochemical properties have been studied. The modified electrode gives a relative reversible redox peaks in 0.1 mol/L phosphate buffer solution (pH 7.0) over the potential range from 0.0 to 0.5 V (vs. Ag/AgCl), which the formal potential is 0.250 V (vs. Ag/AgCl). The formal potential shifts negatively as pH values increased over the range of 5.0 to 8.0. The linear regression equation is E-0'=0.6233-0.05996 pH, R=0.9969, The apparent electron transfer rate constant (K-s) was 12. 3 s(-1), The electrode reaction contain two electrons and two protons process. The caffeic acid modified electrode shows electrocatalytic activity for oxidation of dihydronicotinamide adenine dinucleotide in 0.1 mol/L pH 7.0 PBS. The peak currents were proportional to the concentrations of the dihydronicotinamide adenine dinucleotide in the range of 0.1similar to6.0 mmol/L. The mechanism of electrode reaction has been discussed in this paper.
出处 《分析化学》 SCIE EI CAS CSCD 北大核心 2003年第11期1380-1384,共5页 Chinese Journal of Analytical Chemistry
基金 国家自然科学基金 (No .2 0 175 0 2 5 2 9875 0 2 7) 电分析化学国家重点实验室资助课题 国家"九五"科技攻关重点项目 (No .96 A2 3 0 1 0 6)资助课题
关键词 咖啡酸 玻碳修饰电极 烟酰胺腺嘌呤二核苷酸 电催化氧化 电沉积 辅酶 dihydronicotinamide adenine dinucleotide caffeic acid chemically modified electrode glassy carbon electrode electrodeposited electrocatalysis
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  • 1[1]Miller L L, Valentine J R. J.Am.Chem.Soc, 1988, 110 (12): 3982~3989
  • 2[2]Delia Dicu, Liana Muresan. Electrochimica Acta, 2000, 45:3951~3957
  • 3[3]Bjorn Persson, Lo Gorton. J. Electroanal. Chem., 1990, 292:115~138
  • 4[4]Ionel Catalin Popescu, Elena Dominguez, Arantzazu Narvaez. J. Electroanal. Chem., 1999, 464:208~214
  • 5[7]Cai C X, Xue K H. Anal. Chim. Acta, 1997, 343(1/2): 69~77
  • 6[8]Chi Quijin, Dong Shaojun. Analyst, 1994, 119(15): 1063~1066
  • 7[9]Pariente F, Lorenzo F, Abruna H D. Anal. Chem., 1994, 66(23):4337~4344
  • 8[10]Pariente F, Tobalina F, Darder M. Anal. Chem., 1996, 68(18): 3135~3142
  • 9[11]Hapiot P, Neudeck A, Pinson J. J. Electroanal. Chem., 1996, 405,169~176
  • 10[12]Pariente F, Tobalina F, Morenno G. Anal. Chem., 1997, 69 (22), 4065~4075

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