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基于铈和银共掺杂的五氧化二锑的高灵敏度光电化学神经元特异性烯醇化酶分析

Highly sensitive photoelectrochemical neuron specific enolase analysis based on cerium and silver Co-Doped SbWO.

机构信息

Provincial Key Laboratory of Rural Energy Engineering in Yunnan, Yunnan Normal University, Kunming, 650500, China; Collaborative Innovation Center for Green Chemical Manufacturing and Accurate Detection, School of Chemistry and Chemical Engineering, Key Laboratory of Interfacial Reaction & Sensing Analysis in Universities of Shandong, University of Jinan, Jinan, 250022, China.

Collaborative Innovation Center for Green Chemical Manufacturing and Accurate Detection, School of Chemistry and Chemical Engineering, Key Laboratory of Interfacial Reaction & Sensing Analysis in Universities of Shandong, University of Jinan, Jinan, 250022, China.

出版信息

Biosens Bioelectron. 2022 May 1;203:114047. doi: 10.1016/j.bios.2022.114047. Epub 2022 Jan 29.

Abstract

A signal-enhanced photoelectrochemical immunoassay technique for detecting neuron specific enolase (NSE) was proposed. As a photoactive matrix, (Ce,Ag):SbWO was firstly investigated via doping Ce and Ag into SbWO. It could be found that the presence of Ce and Ag not only had enormous variation on the morphology of SbWO, but also showed excellent PEC behavior. In order to further improve the visible light utilization rate of (Ce,Ag):SbWO, InS was modified onto the surface of (Ce,Ag):SbWO to enhance visible light absorption. In addition, the CdS/PDA was served as a secondary antibody marker to further amplify signal. Especially, PDA as an electron donor could effectively remove photogenerated holes. Meanwhile, the good matching cascade band-edge levels between CdS and SbWO could promote photoelectron migration, improve the PEC response, and achieve sensitive detection of NSE. Under the selected excellent conditions, the photocurrent can linearly increase with the increase of NSE concentration in the operating range from 0.1 pg/mL to 50 ng/mL, and the limit of detection is 1.57 fg/mL. The constructed immunosensor also exhibits satisfactory stability, selectivity, and reproducibility, and it creates conditions for the detection of other biomolecules.

摘要

提出了一种用于检测神经元特异性烯醇化酶(NSE)的信号增强光电化学免疫分析技术。(Ce,Ag):SbWO 首次被用作光活性基质,通过将 Ce 和 Ag 掺杂到 SbWO 中。可以发现,Ce 和 Ag 的存在不仅对 SbWO 的形态有巨大的变化,而且表现出优异的 PEC 行为。为了进一步提高(Ce,Ag):SbWO 的可见光利用率,InS 被修饰在(Ce,Ag):SbWO 的表面以增强可见光吸收。此外,CdS/PDA 被用作二次抗体标记物以进一步放大信号。特别是 PDA 作为电子供体可以有效地去除光生空穴。同时,CdS 和 SbWO 之间良好的级联能带匹配可以促进光生电子迁移,提高 PEC 响应,实现对 NSE 的灵敏检测。在选择的最佳条件下,光电流可以在 0.1pg/mL 至 50ng/mL 的工作范围内随着 NSE 浓度的增加线性增加,检测限为 1.57fg/mL。所构建的免疫传感器还表现出令人满意的稳定性、选择性和重现性,为其他生物分子的检测创造了条件。

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