Tang Mingyu, Chen Shihong, Yuan Ruo, Chai Yaqin, Gao Fengxian, Xie Yi
Chongqing Key Laboratory of Analytical Chemistry, College of Chemistry and Engineering, Southwest University, Chongqing, PR China.
Anal Sci. 2008 Apr;24(4):487-91. doi: 10.2116/analsci.24.487.
A facile strategy of an amperometric biosensor for hydrogen peroxide based on the direct electrocatalysis of hemoglobin (Hb) immobilized on gold nanoparticles (GNPs)/1,6-diaminohexane (DAH) modified glassy carbon electrode (GCE) has been described. A uniform monolayer film of DAH was initially covalently bound on a GCE surface by virtue of the electrooxidation of one amino group of DAH, and another amino group was modified with GNPs and Hb, successively. The fabrication process was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). The proposed biosensor exhibited an effective and fast catalytic response to the reduction of H2O2 with good reproducibility and stability. A linear relationship existed between the catalytic current and the H2O2 concentration in the range of 1.5x10(-6) to 2.1x10(-3) M with a correlation coefficient of 0.998 (n=24). The detection limit (S/N=3) was 8.8x10(-7) M.
本文描述了一种基于固定在金纳米颗粒(GNPs)/1,6 - 二氨基己烷(DAH)修饰玻碳电极(GCE)上的血红蛋白(Hb)直接电催化的过氧化氢安培生物传感器的简便策略。首先,通过DAH的一个氨基的电氧化将均匀的DAH单分子层膜共价结合在GCE表面,然后另一个氨基依次用GNPs和Hb进行修饰。通过循环伏安法(CV)、电化学阻抗谱(EIS)和扫描电子显微镜(SEM)对制备过程进行了表征。所提出的生物传感器对H2O2的还原表现出有效且快速的催化响应,具有良好的重现性和稳定性。催化电流与H2O2浓度在1.5×10(-6)至2.1×10(-3)M范围内呈线性关系,相关系数为0.998(n = 24)。检测限(S/N = 3)为8.8×10(-7)M。