发光体
化学
电化学发光
钌
纳米技术
生物传感器
组合化学
纳米团簇
发光
色谱法
光电子学
有机化学
催化作用
检出限
生物化学
材料科学
作者
Pei-Xin Yuan,Shushu Song,Jiale Zhan,Can Chen,Ai‐Jun Wang,Jiu‐Ju Feng
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-12-08
卷期号:95 (50): 18572-18578
被引量:14
标识
DOI:10.1021/acs.analchem.3c04423
摘要
Electrochemiluminescence (ECL) has attracted significant interest in the analysis of cancer cells, where the ruthenium(II)-based emitter demonstrates urgency and feasibility to improve the ECL efficiency. In this work, the self-enhanced ECL luminophore was prepared by covalent anchoring of Pd nanoclusters on aminated metal organic frameworks (Pd NCs@MOFs), followed by linkage with bis(2,2′-bipyridine)-5-amino-1,10-phenanthroline ruthenium(II) (RuP). The resultant luminophore showed 214-fold self-magnification in the ECL efficiency over RuP alone, combined by promoting the interfacial photoelectron transfer. The enhanced mechanism through ion annihilation was critically proved by controlled experiments and density functional theory (DFT) calculations. Based on the above, a "signal off" ECL biosensor was built by assembly of tyrosine kinase 7 (PTK-7) aptamer (Apt) on the established sensing platform for analysis of human lung cancer cells (A549). The built sensor showed a lower detection limit of 8 cells mL–1, achieving the single-cell detection. This work reported a self-enhanced strategy for synthesis of advanced ECL emitters, combined by exploring the ECL biosensing devices in the single-cell analysis of cancers.
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