Coreactant-free and single-potential-channel electrochemiluminescence from dual-thiols-stabilizer capped gold nanoclusters and its NIR immunoassay application
{"title":"Coreactant-free and single-potential-channel electrochemiluminescence from dual-thiols-stabilizer capped gold nanoclusters and its NIR immunoassay application","authors":"Mengwei Li, Xuwen Gao, Xiaoxuan Ren, Luyao Ma, Yujiao Wang, Guizheng Zou","doi":"10.1016/j.bios.2025.117617","DOIUrl":null,"url":null,"abstract":"<div><div>Ru(bpy)<sub>3</sub><sup>2+</sup>/tripropylamine (TPrA) is the sole electrochemiluminescence (ECL) system, which is being extensively employed in commercialized In Vitro Diagnosis. The coreactant ECL of Ru(bpy)<sub>3</sub><sup>2+</sup>/TPrA is of a multiple-channel emission and wide electrochemical potential window nature. Herein, a coreactant-free and single-potential-channel ECL strategy is proposed with a biocompatible nano-electrochemiluminophore, i.e., dihydrolipoic acid-capped Au nanoclusters (DHLA-AuNCs) as model, in which the metal-sulfur bonds between two sulfhydryls of DHLA and the Au element enable AuNCs with a S vacancies involved electron-rich and n-type nature for DHLA-AuNCs. The DHLA-AuNCs can be electrochemically oxidized, the annihilation reaction between exogenous holes and endogenous free-electrons can emit a kind of coreactant-free single-potential-channel ECL between +0.70 and + 1.20 V (<em>vs</em> Ag/AgCl) with the maximum emission potential of +0.91 V (<em>vs</em> Ag/AgCl) and the maximum emission wavelength of 778 nm. The ECL can be conveniently achieved, and selectively determine human carcinoembryonic antigen with the linear response range from 20 to 5000 pg/mL and the limit of detection of 5 pg/mL. The coreactant-free and single-potential-channel ECL of DHLA-AuNCs provides an alternative to the coreactant ECL of Ru(bpy)<sub>3</sub><sup>2+</sup>/TPrA for less electrochemical-interference and signal-crosstalk.</div></div>","PeriodicalId":259,"journal":{"name":"Biosensors and Bioelectronics","volume":"286 ","pages":"Article 117617"},"PeriodicalIF":10.7000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosensors and Bioelectronics","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0956566325004919","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Ru(bpy)32+/tripropylamine (TPrA) is the sole electrochemiluminescence (ECL) system, which is being extensively employed in commercialized In Vitro Diagnosis. The coreactant ECL of Ru(bpy)32+/TPrA is of a multiple-channel emission and wide electrochemical potential window nature. Herein, a coreactant-free and single-potential-channel ECL strategy is proposed with a biocompatible nano-electrochemiluminophore, i.e., dihydrolipoic acid-capped Au nanoclusters (DHLA-AuNCs) as model, in which the metal-sulfur bonds between two sulfhydryls of DHLA and the Au element enable AuNCs with a S vacancies involved electron-rich and n-type nature for DHLA-AuNCs. The DHLA-AuNCs can be electrochemically oxidized, the annihilation reaction between exogenous holes and endogenous free-electrons can emit a kind of coreactant-free single-potential-channel ECL between +0.70 and + 1.20 V (vs Ag/AgCl) with the maximum emission potential of +0.91 V (vs Ag/AgCl) and the maximum emission wavelength of 778 nm. The ECL can be conveniently achieved, and selectively determine human carcinoembryonic antigen with the linear response range from 20 to 5000 pg/mL and the limit of detection of 5 pg/mL. The coreactant-free and single-potential-channel ECL of DHLA-AuNCs provides an alternative to the coreactant ECL of Ru(bpy)32+/TPrA for less electrochemical-interference and signal-crosstalk.
期刊介绍:
Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.