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基于 MnO 纳米花作为新型共反应加速剂的用于谷胱甘肽检测的灵敏电致化学发光生物传感器:Ru 配合物/三丙胺体系

Sensitive electrochemiluminescence biosensor for glutathione using MnO nanoflower as novel co-reaction accelerator for Ru complex/tripropylamine system.

机构信息

Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education Chongqing, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education Chongqing, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

出版信息

Anal Chim Acta. 2021 Dec 15;1188:339181. doi: 10.1016/j.aca.2021.339181. Epub 2021 Oct 18.

DOI:10.1016/j.aca.2021.339181
PMID:34794568
Abstract

In this work, MnO nanoflower (NF), as novel and more effective co-reaction accelerator, was applied to construct a new ternary electrochemiluminescence (ECL) system of Ru complex/tripropylamine (TPrA)/MnO NF. Compared with the classic Ru complex/TPrA binary ECL system, the reaction efficiency of co-reactant TPrA in the new ternary ECL system was obviously enhanced, leading to the significantly improved ECL signal by accelerating the dissociation of co-reactants into more active radicals. Then, an ECL biosensor was fabricated based on the proposed ternary ECL system, realizing the sensitive determination of glutathione (GSH). In order to realize the efficient nucleic acid amplification, a certain amount of GSH was firstly converted to a large number of intermediate DNA in assistance of Hg, which acted as walker could walk along with the DNA triplex immobilized on the electrode and cut off the DNA strand (S2) labeled with ferrocene (Fc). Owing to the fact that Fc possessed obvious quenching effect to the ECL of Ru complex labeled on the other side of S2, the ECL signal recovered significantly. Thus, the proposed ECL biosensor achieved the sensitive determination of GSH, and the detection limit was 50 nM.

摘要

在这项工作中,MnO 纳米花(NF)作为新型且更有效的共反应加速剂,被应用于构建 Ru 配合物/三丙胺(TPrA)/MnO NF 的新型三元电化学发光(ECL)体系。与经典的 Ru 配合物/TPrA 二元 ECL 体系相比,共反应物 TPrA 在新三元 ECL 体系中的反应效率明显增强,通过加速共反应物分解为更活跃的自由基,从而显著提高了 ECL 信号。然后,基于所提出的三元 ECL 体系构建了 ECL 生物传感器,实现了对谷胱甘肽(GSH)的灵敏测定。为了实现有效的核酸扩增,首先在 Hg 的辅助下,将一定量的 GSH 转化为大量的中间 DNA,Hg 作为 Walker 可以沿着固定在电极上的三链体 DNA 移动,并切断标记有二茂铁(Fc)的 DNA 链(S2)。由于 Fc 对 S2 另一侧标记的 Ru 配合物的 ECL 具有明显的猝灭作用,因此 ECL 信号显著恢复。因此,所提出的 ECL 生物传感器实现了对 GSH 的灵敏测定,检测限为 50 nM。

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