A highly sensitive electrochemiluminescence immunosensor based on Ru(bpy)32+/PAMG composite carriers and Au-Fc-MOF quenching systems for ultra-trace detection of carcinoembryonic antigen.
{"title":"A highly sensitive electrochemiluminescence immunosensor based on Ru(bpy)<sub>3</sub><sup>2+</sup>/PAMG composite carriers and Au-Fc-MOF quenching systems for ultra-trace detection of carcinoembryonic antigen.","authors":"Baohan Wen, Haoyi Ren, Wenjing Lai, Min Wang, Mingzhe Jiang, Yingying Cheng, Yige Li, Chenglin Hong, Yu Qi","doi":"10.1039/d5ay01289a","DOIUrl":null,"url":null,"abstract":"<p><p>Early cancer diagnosis is crucial due to a significant increase in cancer incidence over the last three decades. A highly sensitive electrochemiluminescence technique was developed for carcinoembryonic antigen (CEA) detection. This method uses Ru(bpy)<sub>3</sub><sup>2+</sup> as the luminescent substance and a silica and polyacrylamide gel composite as the carrier. Ru(bpy)<sub>3</sub><sup>2+</sup> is loaded into it to prevent its leakage. At the same time, biological molecules such as antibodies or antigens are immobilized, thereby improving the stability and reaction activity of the system. Additionally, Au-Fc-MOF was synthesized to act as a quencher and secondary antibody label, absorbing the emitted energy from the ECL emitter to improve detection accuracy across various CEA concentrations. Potassium persulfate was employed as a co-reactant to generate SO<sub>4</sub>˙<sup>-</sup> radicals, intensifying the luminescence output of the system. The findings revealed that the developed immunosensor exhibited strong linearity within the concentration range of 10<sup>-5</sup> ng mL<sup>-1</sup> to 10 ng mL<sup>-1</sup>, with a remarkably low detection limit of 5.03 fg mL<sup>-1</sup>. This electrochemical luminescence immunosensor, characterized by its simple preparation, cost-effectiveness, and superior performance, demonstrates significant potential in advancing early CEA detection methodologies.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Methods","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ay01289a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Early cancer diagnosis is crucial due to a significant increase in cancer incidence over the last three decades. A highly sensitive electrochemiluminescence technique was developed for carcinoembryonic antigen (CEA) detection. This method uses Ru(bpy)32+ as the luminescent substance and a silica and polyacrylamide gel composite as the carrier. Ru(bpy)32+ is loaded into it to prevent its leakage. At the same time, biological molecules such as antibodies or antigens are immobilized, thereby improving the stability and reaction activity of the system. Additionally, Au-Fc-MOF was synthesized to act as a quencher and secondary antibody label, absorbing the emitted energy from the ECL emitter to improve detection accuracy across various CEA concentrations. Potassium persulfate was employed as a co-reactant to generate SO4˙- radicals, intensifying the luminescence output of the system. The findings revealed that the developed immunosensor exhibited strong linearity within the concentration range of 10-5 ng mL-1 to 10 ng mL-1, with a remarkably low detection limit of 5.03 fg mL-1. This electrochemical luminescence immunosensor, characterized by its simple preparation, cost-effectiveness, and superior performance, demonstrates significant potential in advancing early CEA detection methodologies.
早期癌症诊断是至关重要的,因为在过去三十年中癌症发病率显著增加。建立了一种检测癌胚抗原(CEA)的高灵敏度电化学发光技术。该方法以Ru(bpy)32+为发光物质,二氧化硅-聚丙烯酰胺凝胶复合材料为载体。Ru(bpy)32+被装入,以防止其泄漏。同时,将抗体或抗原等生物分子固定化,从而提高了系统的稳定性和反应活性。此外,还合成了Au-Fc-MOF作为猝灭剂和二抗标签,吸收ECL发射器发射的能量,以提高不同CEA浓度下的检测精度。过硫酸钾作为助反应物生成SO4˙自由基,增强了系统的发光输出。结果表明,所研制的免疫传感器在10-5 ng mL-1 ~ 10 ng mL-1的浓度范围内呈良好的线性关系,检出限极低,仅为5.03 fg mL-1。该电化学发光免疫传感器具有制备简单、成本效益高、性能优越等特点,在推进早期CEA检测方法方面具有重要的潜力。