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基于 F、S 共掺杂碳点/铜纳米结构的非酶生物传感器在同时测定血浆中 NADH、多巴胺和尿酸中的应用。

Non-enzymatic biosensor based on F,S-doped carbon dots/copper nanoarchitecture applied in the simultaneous electrochemical determination of NADH, dopamine, and uric acid in plasma.

机构信息

LabNaHm: Multifunctional Hybrid Nanomaterials Laboratory, Engineering School, Mackenzie Presbyterian University, 01302-907 São Paulo, SP, Brazil.

出版信息

Analyst. 2024 Apr 29;149(9):2728-2737. doi: 10.1039/d3an02239k.

Abstract

This work presents the synthesis and characterization of an innovative F,S-doped carbon dots/CuONPs hybrid nanostructure obtained by a direct mixture between F,S-doped carbon dots obtained electrochemically and copper nitrate alcoholic solution. The hybrid nanostructures synthesized were characterized by absorption spectroscopy in the Ultraviolet region (UV-vis), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and different electrochemical techniques. The fluoride and sulfur-doped carbon dots/CuONPs nanostructures were used to prepare a non-enzymatic biosensor on a printed carbon electrode, exhibiting excellent electrocatalytic activity for the simultaneous determination of NADH, dopamine, and uric acid in the presence of ascorbic acid with a detection limit of 20, 80, and 400 nmol L, respectively. The non-enzymatic biosensors were also used to determine NADH, dopamine, and uric acid in plasma, and they did not suffer significant interference from each other.

摘要

这项工作提出了一种新颖的 F、S 掺杂碳点/CuONPs 杂化纳米结构的合成与表征,该结构通过电化学合成的 F、S 掺杂碳点与硝酸铜醇溶液的直接混合获得。所合成的杂化纳米结构通过紫外区(UV-vis)吸收光谱、高分辨率透射电子显微镜(HRTEM)、X 射线光电子能谱(XPS)和不同的电化学技术进行了表征。氟和硫掺杂的碳点/CuONPs 纳米结构被用于在印刷碳电极上制备非酶生物传感器,在抗坏血酸存在下对烟酰胺腺嘌呤二核苷酸(NADH)、多巴胺和尿酸的同时测定表现出优异的电催化活性,检测限分别为 20、80 和 400 nmol L。非酶生物传感器还用于测定血浆中的烟酰胺腺嘌呤二核苷酸(NADH)、多巴胺和尿酸,它们之间没有受到显著的相互干扰。

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