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一种基于石墨烯-全氟磺酸纳米复合膜作为增强传感平台的灵敏无标记安培型癌胚抗原免疫传感器。

A sensitive label-free amperometric CEA immunosensor based on graphene-nafion nanocomposite film as an enhanced sensing platform.

作者信息

Li Yan, Yang Wei-Kang, Fan Man-Qi, Liu Ao

机构信息

Department of Respiratory Medicine, Kunming General Hospital of The People's Liberation Army, PR China.

出版信息

Anal Sci. 2011;27(7):727. doi: 10.2116/analsci.27.727.

Abstract

A novel approach to fabricate a label-free amperometric immunosensor for the detection of carcinoembryonic antigen (CEA) was described. Herein, methylene blue (MB), gold nanoparticles (AuNPs) and carcinoembryonic antibody (anti-CEA) were layer-by-layer assembled on the graphene-Nafion nanocomposite film-modified electrode by means of a self-assembling technique and the opposite-charged adsorption. Subsequently, the stepwise self-assembling procedure of the immunosensor was further characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The factors influencing the performance of the resulting immunosensor were studied in detail. The developed procedure showed improved features, including larger amount and higher immunoactivity of the immobilized antibody and repeatable regeneration of the sensor, as well as direct, rapid and simple determination for the antigen without multiple separation and labeling steps. The immunosensor could detect the target protein in a range of 0.5 to 120 ng/mL with a limit of 0.17 ng/mL (at 3σ). Finally, the immunosensing system was evaluated on several clinical samples. Analytical results were found to be in satisfactory agreement with those detected by the enzyme-linked immunosorbent assay (ELISA) method, indicating that this new method was a promising alternative tool for clinical diagnosis.

摘要

描述了一种用于制备检测癌胚抗原(CEA)的无标记电流型免疫传感器的新方法。在此,通过自组装技术和带相反电荷的吸附作用,将亚甲基蓝(MB)、金纳米颗粒(AuNPs)和癌胚抗体(抗CEA)逐层组装在石墨烯-全氟磺酸纳米复合膜修饰电极上。随后,通过循环伏安法(CV)和电化学阻抗谱(EIS)进一步表征了免疫传感器的逐步自组装过程。详细研究了影响所得免疫传感器性能的因素。所开发的方法具有改进的特性,包括固定化抗体的量更大、免疫活性更高、传感器可重复再生,以及无需多次分离和标记步骤即可直接、快速且简单地测定抗原。该免疫传感器能够在0.5至120 ng/mL的范围内检测目标蛋白,检测限为0.17 ng/mL(3σ)。最后,在多个临床样本上对该免疫传感系统进行了评估。发现分析结果与酶联免疫吸附测定(ELISA)方法检测的结果令人满意地一致,表明这种新方法是一种有前途的临床诊断替代工具。

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