Triple signal-enhanced electrochemiluminescence strategy using iron-based metal-organic frameworks modified with Ru(II) complexes for carcino-embryonic antigen detection

被引:13
|
作者
Zhang, Di [1 ,2 ]
Gao, Min [5 ]
Xue, Xiaodong [4 ]
Ren, Xiang [1 ,2 ]
Feng, Rui [1 ,2 ]
Wu, Dan [1 ,2 ]
Liu, Xuejing [1 ,2 ]
Wei, Qin [1 ,2 ,3 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Collaborat Innovat Ctr Green Chem Mfg & Accurate D, Jinan 250022, Peoples R China
[2] Univ Jinan, Sch Chem & Chem Engn, Key Lab Interfacial React & Sensing Anal Univ Shan, Jinan 250022, Peoples R China
[3] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
[4] Shandong Acad Environm Sci Co Ltd, Jinan 250013, Peoples R China
[5] Qilu Univ Technol, Shandong Acad Sci, State Key Lab Biobased Mat & Green Papermaking, Daxue Rd, Jinan 250353, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Ru(bpy)(3)(2+); Au@MoS2; Electrochemiluminescence; Triple signal-enhanced;
D O I
10.1016/j.talanta.2023.125239
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The development of a highly efficient electrochemiluminescence (ECL) emitter represents an effective strategy for enhancing the sensitivity and repeatability of ECL immunosensors. In this study, a sandwich-type ECL immunosensor with triple enhancement was developed to detect carcino-embryonic antigen (CEA). This sensor is based on a porous structure of iron-based metal-organic framework (NH2-MIL-88(Fe)), encapsulating the luminescent tris(2,2 '-bipyridine)ruthenium (II) (Ru (bpy)(3)(2+)), Au@MoS2 with a 3D nanoflower structure as an enhanced substrate. In this system, the MOFs framework encapsulated luminophore was realized to solve its water solubility to reach stable luminescence, as well as the triple enhancement effect based on the principle of amino catalysis, Mo4+/Mo6+ active site conversion, and gold nanoparticles (Au NPs) promotion, which significantly enhanced the detection sensitivity. Furthermore, the ECL immunosensor demonstrated successful application in the highly sensitive and selective detection of CEA, achieving a detection limit of 38.9 fg mL(-1). The sensor demonstrates remarkable sensitivity, specificity, stability, repeatability, and practicality in the analysis of human serum samples. This investigation presents a highly effective approach for the ultrasensitive detection of trace proteins.
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页数:8
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