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用于多重 miRNA 同时测定的电位分辨电化学发光生物传感器。

Potential-resolved electrochemiluminescence biosensor for simultaneous determination of multiplex miRNA.

机构信息

Institute for Advanced Interdisciplinary Research(iAIR), University of Jinan, Jinan, 250022, PR China.

Department of Medical Laboratory, Shandong Medical College, Jinan, 250002, PR China.

出版信息

Talanta. 2024 Jan 1;266(Pt 2):125063. doi: 10.1016/j.talanta.2023.125063. Epub 2023 Aug 8.

Abstract

The multi-target simultaneous detection strategy based on potential-resolved electrochemiluminescence (ECL) has still been a research hotspot in analytical science, but the limited selection of ECL luminophores hinders the development of this field. Herein, polyethyleneimine functionalized perylene derivatives (PTC-PEI) and luminol functionalized gold nanoparticles (Lu-Au NPs) possessed significantly resolved emission potentials as ECL luminophore. The ternary ECL system was constructed with MoS nanoflowers and KSO as the coreaction accelerator and coreactant respectively, which significantly improved the cathode ECL emission of PTC-PEI. Simultaneously, the anode coreaction accelerator ZnO nanoflowers could promote the anode coreactant dissolved O reduction, and extremely enhanced the anode ECL emission of Lu-Au NPs. The proposed strategy addressed the major technical challenge of cross interference and competition of the coreactants for dual-biomarker detection, thus enabling accurate detection of miRNA-205 and miRNA-21 from 10 fM to 100 nM, with detection limits of 2.57 and 1.15 fM, respectively. In general, this work achieved a single-step synchronous detection of dual biomarkers, providing a new idea for the ECL detection of multiple biomarkers, and having potential value in the clinical diagnosis.

摘要

基于势分辨电致化学发光(ECL)的多靶标同时检测策略仍然是分析科学的研究热点,但 ECL 发光体的有限选择阻碍了该领域的发展。在此,我们将具有明显分辨发射势的聚乙烯亚胺功能化苝衍生物(PTC-PEI)和鲁米诺功能化金纳米粒子(Lu-Au NPs)用作 ECL 发光体。该三元 ECL 体系以 MoS 纳米花和 KSO 分别作为核心反应加速剂和核心反应物构建,显著提高了 PTC-PEI 的阴极 ECL 发射。同时,阳极核心反应加速剂 ZnO 纳米花可以促进阳极核心反应物溶解 O 的还原,极大地增强了 Lu-Au NPs 的阳极 ECL 发射。所提出的策略解决了核心反应物对双生物标志物检测的交叉干扰和竞争的主要技术挑战,从而实现了从 10 fM 到 100 nM 的 miRNA-205 和 miRNA-21 的精确检测,检测限分别为 2.57 和 1.15 fM。总之,本工作实现了双生物标志物的单步同步检测,为多生物标志物的 ECL 检测提供了新的思路,在临床诊断中具有潜在的应用价值。

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