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基于巯基化二茂铁稳定的 Fe₃O₄@Au 纳米粒子与石墨烯片的纳米复合材料的双信号放大平台,用于超灵敏和同时检测抗坏血酸、多巴胺、尿酸和对乙酰氨基酚。

A double signal amplification platform for ultrasensitive and simultaneous detection of ascorbic acid, dopamine, uric acid and acetaminophen based on a nanocomposite of ferrocene thiolate stabilized Fe₃O₄@Au nanoparticles with graphene sheet.

机构信息

Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Ministry of Education, China, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, PR China.

出版信息

Biosens Bioelectron. 2013 Oct 15;48:75-81. doi: 10.1016/j.bios.2013.03.070. Epub 2013 Apr 12.

Abstract

A double signal amplification platform for ultrasensitive and simultaneous detection of ascorbic acid (AA), dopamine (DA), uric acid (UA) and acetaminophen (AC) was fabricated by a nanocomposite of ferrocene thiolate stabilized Fe₃O₄@Au nanoparticles with graphene sheet. The platform was constructed by coating a newly synthesized phenylethynyl ferrocene thiolate (Fc-SAc) modified Fe₃O₄@Au NPs coupling with graphene sheet/chitosan (GS-chitosan) on a glassy carbon electrode (GCE) surface. The Fe₃O₄@Au-S-Fc/GS-chitosan modified GCE exhibits a synergistic catalytic and amplification effect toward AA, DA, UA and AC oxidation. The oxidation peak currents of the four compounds on the electrode were linearly dependent on AA, DA, UA and AC concentrations in the ranges of 4-400 μM, 0.5-50 μM, 1-300 μM and 0.3-250 μM in the individual detection of each component, respectively. By simultaneously changing the concentrations of AA, DA, UA and AC, their electrochemical oxidation peaks appeared at -0.03, 0.15, 0.24 and 0.35 V, and good linear current responses were obtained in the concentration ranges of 6-350, 0.5-50, 1-90 and 0.4-32 μM with the detection limits of 1, 0.1, 0.2 and 0.05 μM (S/N=3), respectively.

摘要

一种双信号放大平台,通过将巯基化二茂铁稳定的 Fe₃O₄@Au 纳米粒子与石墨烯片复合,用于超灵敏和同时检测抗坏血酸(AA)、多巴胺(DA)、尿酸(UA)和对乙酰氨基酚(AC)。该平台是通过将新合成的苯乙炔基二茂铁巯基化物(Fc-SAc)修饰的 Fe₃O₄@Au NPs 与石墨烯片/壳聚糖(GS-chitosan)偶联在玻碳电极(GCE)表面上构建的。Fe₃O₄@Au-S-Fc/GS-chitosan 修饰的 GCE 对 AA、DA、UA 和 AC 的氧化表现出协同催化和放大效应。在单独检测每种成分时,四种化合物在电极上的氧化峰电流分别在 AA、DA、UA 和 AC 浓度为 4-400 μM、0.5-50 μM、1-300 μM 和 0.3-250 μM 的范围内呈线性依赖。通过同时改变 AA、DA、UA 和 AC 的浓度,它们的电化学氧化峰出现在-0.03、0.15、0.24 和 0.35 V 处,并且在 6-350、0.5-50、1-90 和 0.4-32 μM 的浓度范围内获得了良好的线性电流响应,检测限分别为 1、0.1、0.2 和 0.05 μM(S/N=3)。

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