化学
电化学发光
纳米团簇
检出限
线性范围
电子转移
组合化学
生物传感器
氧化还原
配体(生物化学)
聚糖
能量转移
纳米颗粒
纳米技术
胶体金
适体
分析物
电化学
共价键
生物相容性材料
电极
作者
Na Li,Jingui Chen,Yu Du,Dehao Jia,Hongying Jia,Dawei Fan,Qin Wei
标识
DOI:10.1021/acs.analchem.5c05119
摘要
Gold nanoclusters (AuNCs) protected by sulfhydryl ligands exhibit excellent optical properties and good biocompatibility. However, the inefficient charge transfer during redox reactions, stemming from free vibration and rotation of the ligands, limits their application in electrochemiluminescence (ECL). To address this, glutathione-protected AuNCs (GSH-AuNCs) were immobilized onto Fe-MIL-88A nanoparticles, serving as the ECL emitter. The GSH-AuNCs@Fe-MIL-88A composite effectively suppressed energy dissipation caused by ligand motion, while simultaneously enhancing charge transfer and reducing nonradiative decay pathways through structural stabilization. Furthermore, Co-doped CdO was employed as a co-reaction accelerator to promote the generation of radical intermediates from N, N -diisopropylethylamine, thereby amplifying the ECL signal. Leveraging this enhanced system, a highly sensitive ECL immunosensor was constructed for the detection of the glycan antigen CA15-3. This immunosensor demonstrated excellent stability, reproducibility, and selectivity. Meanwhile, it exhibited a wide linear range from 0.1 pM to 100 nM for CA15-3 detection, with an impressively low limit of detection of 0.02 pM (S/N = 3). This work provides a novel strategy for utilizing gold nanoclusters in ECL applications and can be readily extended to detect other disease biomarkers.
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