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基于原位生成的 1-萘酚作为电活性物质和氧化石墨烯及负载 Pt 纳米粒子的 CeO2 纳米复合材料作为信号增强剂的电化学免疫传感器的放大。

An amplified electrochemical immunosensor based on in situ-produced 1-naphthol as electroactive substance and graphene oxide and Pt nanoparticles functionalized CeO2 nanocomposites as signal enhancer.

机构信息

Key Laboratory of Luminescence and Real-Time Analytic chemistry, (southwest university) Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

Key Laboratory of Luminescence and Real-Time Analytic chemistry, (southwest university) Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Biosens Bioelectron. 2015 Jul 15;69:321-7. doi: 10.1016/j.bios.2015.01.035. Epub 2015 Jan 17.

Abstract

In this work, an amplified electrochemical immunosensor based on 1-naphthol as electroactive substance and Pt/CeO2/GO composites as catalytic amplifier was constructed for sensitive detection influenza. Through "sandwich" reaction, the Pt/CeO2/GO functionalized bioconjugates were captured on electrode surface and the electrochemical signal directly originated from 1-naphthol, which was in situ produced with high local concentration though the hydrolysis of 1-naphthyl phosphate catalyzed by ALP. Then, 1-naphthol as new reactant was oxidized by Pt/CeO2/GO composites with outstanding catalytic performance, resulting in detection signal amplification. In addition, as compared to label electroactive substance to antibodies, a simplified preparative step of immunosensor could be achieved because the signal probe get rid of introducation other electroactive substances. The proposed immunosensor achieved a linear range of 1.0×10(-3)-1.0ngmL(-1) and 5.0 to 1.0×10(2)ngmL(-1) with a detection limit of 0.43pgmL(-1) (defined as S/N=3).

摘要

在这项工作中,构建了基于 1-萘酚作为电活性物质和 Pt/CeO2/GO 复合材料作为催化放大器的放大电化学免疫传感器,用于灵敏检测流感。通过“三明治”反应,将 Pt/CeO2/GO 功能化的生物缀合物捕获在电极表面,并且电化学信号直接源于 1-萘酚,其通过 ALP 催化的 1-萘磷酸酯的水解原位产生,具有高局部浓度。然后,Pt/CeO2/GO 复合材料对 1-萘酚进行氧化,具有出色的催化性能,从而实现检测信号放大。此外,与将标记电活性物质标记到抗体相比,由于信号探针摆脱了引入其他电活性物质,因此可以简化免疫传感器的制备步骤。所提出的免疫传感器的线性范围为 1.0×10(-3)-1.0ngmL(-1)和 5.0 至 1.0×10(2)ngmL(-1),检测限为 0.43pgmL(-1)(定义为 S/N=3)。

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