Particle Size-Controlled Oxygen Reduction and Evolution Reaction Nanocatalysts Regulate Ru(bpy) 3 2+ ’s Dual-potential Electrochemiluminescence for Sandwich Immunoassay

Author:

Wang Shijun1,Zhu Shu1,Kang Ziqi1,Wang Xiangxiu2,Deng Zixin1,Hu Kun1,Hu Jianjun3,Liu Xiancheng2,Wang Guixue24,Zang Guangchao145,Zhang Yuchan14

Affiliation:

1. Institute of Life Science and Laboratory of Tissue and Cell Biology, Lab Teaching & Management Center, Chongqing Medical University, Chongqing 400016, China.

2. Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China.

3. Department of Pathology, Guizhou Provincial People’s Hospital, Guiyang, Guizhou 550002, China.

4. Jinfeng Laboratory, Chongqing 401329, China.

5. Department of Pathophysiology, Chongqing Medical University, Chongqing 400016, China.

Abstract

Multiple signal strategies remarkably improve the accuracy and efficiency of electrochemiluminescence (ECL) immunoassays, but the lack of potential-resolved luminophore pairs and chemical cross talk hinders their development. In this study, we synthesized a series of gold nanoparticles (AuNPs)/reduced graphene oxide (Au/rGO) composites as adjustable oxygen reduction reaction and oxygen evolution reaction catalysts to promote and modulate tris(2,2′-bipyridine) ruthenium(II) (Ru(bpy) 3 2+ )’s multisignal luminescence. With the increase in the diameter of AuNPs (3 to 30 nm), their ability to promote Ru(bpy) 3 2+ ’s anodic ECL was first impaired and then strengthened, and cathodic ECL was first enhanced and then weakened. Au/rGOs with medium-small and medium-large AuNP diameters remarkably increased Ru(bpy) 3 2+ ’s cathodic and anodic luminescence, respectively. Notably, the stimulation effects of Au/rGOs were superior to those of most existing Ru(bpy) 3 2+ co-reactants. Moreover, we proposed a novel ratiometric immunosensor construction strategy using Ru(bpy) 3 2+ ’s luminescence promoter rather than luminophores as tags of antibodies to achieve signal resolution. This method avoids signal cross talk between luminophores and their respective co-reactants, which achieved a good linear range of 10 −7 to 10 −1 ng/ml and a limit of detection of 0.33 fg/ml for detecting carcinoembryonic antigen. This study addresses the previous scarcity of the macromolecular co-reactants of Ru(bpy) 3 2+ , broadening its application in biomaterial detection. Furthermore, the systematic clarification of the detailed mechanisms for converting the potential-resolved luminescence of Ru(bpy) 3 2+ could facilitate an in-depth understanding of the ECL process and should inspire new designs of Ru(bpy) 3 2+ luminescence enhancers or applications of Au/rGOs to other luminophores. This work removes some impediments to the development of multisignal ECL biodetection systems and provides vitality into their widespread applications.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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