Self-enhanced Electrochemiluminescence Luminophore Based on Pd Nanocluster-Anchored Metal Organic Frameworks via Ion Annihilation for Sensitive Cell Assay of Human Lung Cancer

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 nanoc...

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Published inAnalytical chemistry (Washington) Vol. 95; no. 50; pp. 18572 - 18578
Main Authors Yuan, Pei-Xin, Song, Shu-Shu, Zhan, Jiale, Chen, Can, Wang, Ai-Jun, Feng, Jiu-Ju
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 19.12.2023
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Summary: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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content type line 23
ISSN:0003-2700
1520-6882
DOI:10.1021/acs.analchem.3c04423