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基于金纳米粒子修饰的 MoS 纳米片和杂交链式反应的电化学三明治免疫法检测胰岛素

Electrochemical sandwich immunoassay for insulin detection based on the use of gold nanoparticle-modified MoS nanosheets and the hybridization chain reaction.

机构信息

Medical Examination Centre, the First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.

Department of Endocrinology, the First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.

出版信息

Mikrochim Acta. 2018 Dec 7;186(1):6. doi: 10.1007/s00604-018-3124-8.

Abstract

A sandwich-type of electrochemical immunoassay is described for the determination of insulin. It is based on the use of a glassy carbon electrode that was modified with MoS nanosheets decorated with gold nanoparticles (AuNPs) to immobilize a large amount of first antibody (Ab). Following exposure to insulin, secondary antibody (Ab) that was cross-linked to a DNA initiator strand (T) to form an Ab@T conjugate was added to undergo a sandwich immunoreaction. Subsequently, the long dsDNA concatemer was formed by a hybridization chain reaction between Ab@T and auxiliary probes (H, H). Finally, the electrochemical probe ruthenium(II) hexaammine was intercalated into the dsHCR products via electrostatic interaction between the anionic DNA phosphate backbones and the cationic probe. The electrochemical response, best measured at a potential of around -0.21 V (vs Ag/AgCl) has a dynamic range that extends from 0.1 pmol L to 1 nmol L insulin, and the detection limit is as low as 50 fmol L. The assay was acceptably specific, reproducible and stable. In our perception, it represents a viable new tool for determination of this important clinical parameter. Graphical abstract Schematic of a sandwich-type of electrochemical immunoassay for the determination of insulin based on the use of MoS nanosheets modified with gold nanoparticles (AuNP@MoS) and hybridization chain reaction (HCR).

摘要

一种三明治型电化学免疫分析方法被用于胰岛素的测定。它基于使用玻碳电极,该电极经过修饰,纳米二硫化钼(MoS)负载金纳米粒子(AuNPs),以固定大量的第一抗体(Ab)。在与胰岛素接触后,将交联到 DNA 引发子链(T)上的第二抗体(Ab)添加到 Ab@T 共轭物中,以进行三明治免疫反应。随后,Ab@T 和辅助探针(H、H)之间的杂交链式反应形成长的 dsDNA 连接体。最后,电化学探针钌(II)六氨通过阴离子 DNA 磷酸骨架与阳离子探针之间的静电相互作用插入到 dsHCR 产物中。电化学响应,最佳测量电位约为-0.21 V(相对于 Ag/AgCl),其动态范围从 0.1 pmol L 延伸到 1 nmol L 胰岛素,检测限低至 50 fmol L。该测定方法具有可接受的特异性、重现性和稳定性。在我们看来,它代表了一种用于测定这种重要临床参数的可行的新工具。示意图基于使用金纳米粒子(AuNP@MoS)和杂交链式反应(HCR)修饰的纳米二硫化钼(MoS)的三明治型电化学免疫分析测定胰岛素的示意图。

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