Hydrogen-Bond-Induced Melem Assemblies to Resist Aggregation-Caused Quenching for Ultrasensitive ECL Detection of COVID-19 Antigen

化学 抵抗 猝灭(荧光) 氢键 光化学 纳米技术 荧光 分子 有机化学 量子力学 物理 材料科学 图层(电子)
作者
Hao-Tian Zhu,Jingyi Bao,Jinwei Kang,Ai‐Jun Wang,Pei-Xin Yuan,Jiu‐Ju Feng
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:96 (48): 19038-19046 被引量:8
标识
DOI:10.1021/acs.analchem.4c04016
摘要

Nowadays, aggregation-caused quenching (ACQ) of organic molecules in aqueous media seriously restricts their analytical and biomedical applications. In this work, hydrogen bond (H-bond) was utilized to resist the ACQ effect of 2,5,8-triamino-1,3,4,6,7,9,9b-heptaazaphenalene (Melem) as an advanced electrochemiluminescence (ECL) luminophore, whose ECL process was carefully studied in an aqueous K2S2O8 system coupled with electron paramagnetic resonance (EPR) measurements. Notably, the H-bond-induced Melem assemblies (Melem-H) showed 16.6-fold enhancement in the ECL signals as compared to the Melem aggregates (Melem-A), combined by elaborating the enhanced mechanism. On such basis, the effective ECL signal transduction was in situ achieved through the specific recognition of the double-stranded DNA embedded in Melem-H assemblies (Me-dsDNA) with spike protein (SP) of coronavirus disease 2019 (COVID-19). For that, such an ECL biosensor showed a wider linear range (1.0-125.0 pg mL-1) with a lower limit of detection (LOD) down to 0.45 pg mL-1, which also displayed acceptable results in analysis of human nasal swab samples. Therefore, the work provides a distinctive insight on addressing the ACQ effect and broadening the application scope of the organic emitter and offers a simple platform for biomedical detection.
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