Antioxidant Cascade Modulated Electrochemiluminescence by a Biomimetic Metal-Organic Framework with Dual Enzymatic Activity for Disease Marker Immunoassays

被引:12
|
作者
Fang, Jinglong [1 ]
Dai, Li [1 ]
Feng, Ruiqing [1 ]
Ren, Xiang [1 ]
Wu, Dan [1 ]
Cao, Wei [1 ]
Wei, Qin [1 ,2 ]
Ma, Hongmin [1 ]
机构
[1] Univ Jinan, Key Lab Interfacial React & Sensing Anal Univ Sha, Sch Chem & Chem Engn, Jinan 250022, Peoples R China
[2] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
基金
中国国家自然科学基金;
关键词
CHEMILUMINESCENCE;
D O I
10.1021/acs.analchem.3c03205
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
High-performance electrochemiluminescence is a significant approach for the examination of disease biomarkers, and the utilization of innovative electrochemiluminescence detection systems represents a viable strategy to enhance the efficacy of ECL analysis. In this work, the biomimetic engineering metal-organic framework (MOF-818) has realized the ultrasensitive ECL immunoassay of disease markers based on the guidance of the free radical scavenging strategy provided by the antioxidant cascade. Initially, we synthesized a hydrogen-bonded organic framework (HOF) consisting of luminol and three active ligands based on simple room-temperature self-assembly. The luminol-HOF (L-HOF) showed more stable and brighter ECL luminescence activity than the monomer due to the nano-confinement enhancement of the coordinated luminol units. Subsequently, MOF-818 with biomimetic superoxide dismutase (SOD) and catalase (CAT) activities were recruited for the first time as quenching agents for sandwich immunoassay mode. The enzyme activity leads to the reverse transformation of superoxide anion radicals (O-2(-)) and further antioxidant decomposition, decreasing in the responsiveness of luminol ECL signals. Using carcinoembryonic antigen (CEA) as an analytical model, a detection limit of 0.457 pg/mL was obtained within a detection range of 0.001-50 ng/mL. We believe that this novel sandwich sensing model based on enzyme activity provides a meaningful potential tool for precise detection, expanding the broader application of nanoenzymes in analysis.
引用
收藏
页码:14143 / 14149
页数:7
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