Tang Lin, Zeng Guangming, Shen Guoli, Zhang Yi, Li Yuanping, Fan Changzheng, Liu Can, Niu Chenggang
College of Environmental Science and Engineering, Hunan University, Changsha, 410082, China.
Anal Bioanal Chem. 2009 Mar;393(6-7):1677-84. doi: 10.1007/s00216-008-2560-4. Epub 2008 Dec 20.
In this work, an electrochemical dihydronicotinamide adenine dinucleotide (NADH) sensor based on the catalytic growth of Au nanoparticles (Au NPs) on glassy carbon electrode was developed. Catalyzed by Au NPs immobilized on pretreated glassy carbon electrode, the reduction of AuCl(4)(-) in the presence of hydroquinone and cetyltrimethyl ammonium chloride led to the formation of enlarged Au NPs on the electrode surface. Spectrophotometry and high-resolution scanning electronic microscope (SEM) analysis of the sensor morphologies before and after biocatalytic reaction revealed a diameter growth of the nanoparticles. The catalytic growth of Au NPs on electrode surface remarkably facilitated the electron transfer and improved the performance of the sensor. Under optimal conditions, NADH could be detected in the range from 1.25 x 10(-6) to 3.08 x 10(-4) M, and the detection limit was 2.5 x 10(-7) M. The advantages of the proposed sensor, such as high precision and sensitivity, fast response, low cost, and good storage stability, made it suitable for on-line detection of NADH in complex biological systems and contaminant degradation processes.
在本工作中,开发了一种基于金纳米颗粒(Au NPs)在玻碳电极上催化生长的电化学二氢烟酰胺腺嘌呤二核苷酸(NADH)传感器。在对苯二酚和十六烷基三甲基氯化铵存在的情况下,固定在预处理玻碳电极上的Au NPs催化AuCl(4)(-)的还原,导致电极表面形成尺寸增大的Au NPs。对生物催化反应前后传感器形态进行的分光光度法和高分辨率扫描电子显微镜(SEM)分析显示,纳米颗粒的直径有所增长。电极表面Au NPs的催化生长显著促进了电子转移,提高了传感器的性能。在最佳条件下,可检测到的NADH浓度范围为1.25×10(-6)至3.08×10(-4) M,检测限为2.5×10(-7) M。该传感器具有高精度、高灵敏度、响应快、成本低和储存稳定性好等优点,适用于复杂生物体系和污染物降解过程中NADH的在线检测。