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基于导电碳纳米粒子的电化学免疫传感器,使用不规则形状的金纳米粒子标记的酶联抗体作为信号增强剂,提高了对甲胎蛋白的灵敏度。

Conductive carbon nanoparticles-based electrochemical immunosensor with enhanced sensitivity for alpha-fetoprotein using irregular-shaped gold nanoparticles-labeled enzyme-linked antibodies as signal improvement.

机构信息

Key Laboratory of Analysis and Detection for Food Safety (Ministry of Education and Fujian Province), Department of Chemistry, Fuzhou University, Fuzhou, China.

出版信息

Biosens Bioelectron. 2010 Aug 15;25(12):2657-62. doi: 10.1016/j.bios.2010.04.039. Epub 2010 May 4.

DOI:10.1016/j.bios.2010.04.039
PMID:20483583
Abstract

A new electrochemical immunoassay protocol for sensitive detection of alpha-fetoprotein (AFP, as a model) is designed using carbon nanoparticles (CNPs)-functionalized biomimetic interface as immunosensing probe and irregular-shaped gold nanoparticles (ISNGs)-labeled horseradish peroxidase-anti-AFP conjugates (HRP-anti-AFP-ISNG) as trace label. The low-toxic and high-conductive CNPs provided a high capacity nanoparticulate immobilization surface and a facile pathway for electron transfer. In comparison with conventional label methods, i.e. spherical gold nanoparticles-labeled HRP-anti-AFP and HRP-labeled anti-AFP, the electrochemical immunosensor using HRP-anti-AFP-ISNGs as trace labels exhibited high bioelectrocatalytic response toward enzyme substrate and a wide dynamic range from 0.02 to 4.0 ng/mL with a low detection limit of 10 pg/mL toward AFP (at 3sigma). The developed immunoassay method showed good selectivity and acceptable reproducibility. Clinical serum samples with various AFP concentrations were evaluated by using the electrochemical immunosensor and the referenced enzyme-linked immunosorbent assay (ELISA), respectively, and received in good accordance with results obtained from these two methods.

摘要

一种新的电化学免疫分析方案,用于灵敏检测甲胎蛋白(AFP,作为模型),使用碳纳米粒子(CNPs)功能化仿生界面作为免疫传感探针和不规则形状的金纳米粒子(ISNGs)标记辣根过氧化物酶-抗 AFP 缀合物(HRP-anti-AFP-ISNG)作为示踪标记物。低毒高导电性的 CNPs 提供了高容量的纳米颗粒固定化表面和电子转移的简便途径。与传统的标记方法相比,即球形金纳米粒子标记的 HRP-anti-AFP 和 HRP 标记的抗 AFP,使用 HRP-anti-AFP-ISNGs 作为示踪标记物的电化学免疫传感器对酶底物表现出高生物电化学催化响应,并且对 AFP 的动态范围从 0.02 到 4.0 ng/mL,检测限低至 10 pg/mL(3sigma)。所开发的免疫分析方法表现出良好的选择性和可接受的重现性。使用电化学免疫传感器和参考酶联免疫吸附测定(ELISA)分别评估了具有不同 AFP 浓度的临床血清样本,并且与这两种方法的结果非常吻合。

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