Department of Materials Science and Engineering, Sharif University of Technology, Azadi Avenue, P.O. Box 11365-9466, Tehran, Iran.
Institute for Nanoscience and Nanotechnology, Sharif University of Technology, Azadi Avenue, P.O. Box 11365-9466, Tehran, Iran.
Mikrochim Acta. 2018 Feb 14;185(3):178. doi: 10.1007/s00604-018-2722-9.
The authors demonstrate efficient direct electron transfer from the enzyme glucose oxidase to vertically aligned gold nanorods with a diameter of ~160 nm and a length of ~2 μm that are covalently linkage to a 3-dimensional network of reduced graphene oxide nanosheets. The assembly can be prepared by a 2-step electrochemical procedure. This hybrid structure holds the enzyme in a favorable position while retaining its functionality that ultimately provides enhanced performance for enzymatic sensing of glucose without utilizing mediators. The nanorod assembly was applied to the voltammetric detection of glucose. Figures of merit include an electrochemical sensitivity of 12 μA·mM·cm (obtained from cathodic peak current at a voltage of -0.45 V vs. Ag/AgCl), a 3 μM detection limit (at signal/noise = 3), and a wide linear range (0.01-7 mM). The hybrid nanostructure has a heterogeneous electron transfer rate constant (k) of 2.9 s. The high electrochemical activity is attributed to the synergistic effect of a large active surface and an enhanced electron transfer efficiency due to covalent amide linkage. Graphical Abstract Schematic of the procedure utilized for the fabrication of an electrochemical biosensor based on gold nanorods (AuNRs) modified with a reduced graphene oxide (rGO)/glucose oxidase (GOx) conjugate. The enzyme electrode was employed to the determination of glucose by differential pulse voltammetry.
作者展示了葡萄糖氧化酶与垂直排列的金纳米棒之间的有效直接电子转移,金纳米棒的直径约为 160nm,长度约为 2μm,与还原氧化石墨烯纳米片的三维网络通过共价键连接。该组装体可以通过两步电化学程序制备。这种混合结构将酶保持在有利的位置,同时保留其功能,最终为葡萄糖的酶促传感提供了增强的性能,而无需使用介质。纳米棒组装体被应用于葡萄糖的伏安检测。性能指标包括电化学灵敏度为 12μA·mM·cm(在相对于 Ag/AgCl 的-0.45V 电压下从阴极峰电流获得),检测限为 3μM(信号/噪声=3),线性范围宽(0.01-7mM)。该混合纳米结构的异质电子转移速率常数(k)为 2.9s。高电化学活性归因于大的活性表面积和由于共价酰胺键合而增强的电子转移效率的协同效应。