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基于 MnS:CdS@ZnS 核壳量子点的高灵敏电化学发光法用于 microRNA 的超灵敏检测。

Highly Efficient Electrochemiluminescence of MnS:CdS@ZnS Core-Shell Quantum Dots for Ultrasensitive Detection of MicroRNA.

机构信息

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

出版信息

Anal Chem. 2022 May 10;94(18):6874-6881. doi: 10.1021/acs.analchem.2c00970. Epub 2022 Apr 28.

Abstract

In this work, a novel electrochemiluminescence (ECL) biosensor was developed for ultrasensitive detection of microRNA let-7a (miRNA let-7a) based on MnS:CdS@ZnS core-shell quantum dots (QDs) as ECL luminophores with high ECL efficiency. Impressively, compared to the CdS:Mn@ZnS QDs prepared by ionic doping with ECL efficiency of 0.87%, MnS:CdS@ZnS QDs synthesized by bimetallic clusters (CdMnO) doping exhibited high ECL efficiency of up to 15.84% with SO as cathodic coreactant due to the elimination of the dopants size mismatch and "self-purification" effect, which could achieve the surface defect passivation of MnS:CdS@ZnS QDs for effectively improving the ECL emission. Furthermore, with the help of strand displacement amplification (SDA), the trace target miRNA let-7a was able to be converted to a number of output DNA labeled with ferrocene (Fc) to construct an ultrasensitive ECL biosensor. The well-designed ECL biosensor for miRNA let-7a exhibited high stability and excellent sensitivity of a concentration variation from 10 aM to 1 nM and a low detection limit of 4.1 aM, which was further applied to the analysis of miRNA let-7a from cancer cell (MCF-7) lysate. Thus, this strategy provides a novel method to prepare high-efficient ECL emitters for the construction of ECL biosensing platforms in biological fields and clinical diagnosis.

摘要

在这项工作中,开发了一种基于 MnS:CdS@ZnS 核壳量子点 (QDs) 的新型电致化学发光 (ECL) 生物传感器,用于超灵敏检测 microRNA let-7a (miRNA let-7a)。令人印象深刻的是,与通过离子掺杂制备的 ECL 效率为 0.87%的 CdS:Mn@ZnS QDs 相比,MnS:CdS@ZnS QDs 采用双金属簇 (CdMnO) 掺杂,由于消除了掺杂剂尺寸不匹配和“自净化”效应,表现出高达 15.84%的 ECL 效率,SO 作为阴极共反应物,这可以实现 MnS:CdS@ZnS QDs 的表面缺陷钝化,从而有效提高 ECL 发射。此外,借助链置换扩增 (SDA),痕量靶标 miRNA let-7a 可以转化为大量输出的 DNA 标记有二茂铁 (Fc),以构建超灵敏的 ECL 生物传感器。设计良好的 miRNA let-7a ECL 生物传感器具有高稳定性和优异的灵敏度,浓度变化范围从 10 aM 到 1 nM,检测限低至 4.1 aM,进一步应用于癌细胞 (MCF-7) 裂解物中 miRNA let-7a 的分析。因此,该策略为构建生物领域和临床诊断中的 ECL 生物传感平台提供了一种制备高效 ECL 发射器的新方法。

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