Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Biosens Bioelectron. 2010 Mar 15;25(7):1851-5. doi: 10.1016/j.bios.2009.12.027. Epub 2009 Dec 29.
A new approach was established to construct a sandwich-type electrochemiluminescence (ECL) immunosensor by using Ru(bpy)(3)(2+)-doped silica (abbreviated as Ru-SiO(2)) nanoparticles to label secondary antibody. Firstly, carboxylate-terminated multi-walled carbon nanotubes (MWCNTs) were modified on the electrode to bond with avidin. Subsequently, biotinylated antibodies were immobilized on the surface of the electrode by employing the specific interaction of biotin/avidin and the non-covalent and covalent conjugation function of MWCNTs. Later, the electrode was incubated with antigen of mouse IgG and then reacted with the secondary antibody which was labeled by Ru-SiO(2). Accordingly, through the ECL response of Ru-SiO(2) and tripropylamine (TPA), a strong ECL signal was obtained and an amplification analysis of protein interaction was achieved. The present immunosensor showed a wide linear range of 0.05-200.00 ng mL(-1) for detecting mouse IgG, with a low detection limit of 17 pg mL(-1). There was a 4-300-fold improvement in detection limit compared with other similar studies. The morphologies of Ru-SiO(2) nanoparticles were characterized by using transmission electronic microscopy (TEM). The fabrication process of the immunosensor was studied by cyclic voltammetry (CV) and the performance of the immunosensor was monitored with an electrochemiluminescence analyzer. This new strategy for preparation of the ECL immunosensor could be easily realized and has potential application in ultrasensitive bioassays.
建立了一种新的三明治型电化学发光(ECL)免疫传感器的构建方法,该方法使用 Ru(bpy)(3)(2+)-掺杂二氧化硅(缩写为 Ru-SiO(2)) 纳米粒子标记二级抗体。首先,羧基化多壁碳纳米管(MWCNTs)被修饰在电极上以与亲和素结合。随后,通过生物素/亲和素的特异性相互作用和 MWCNTs 的非共价和共价共轭功能,将生物素化抗体固定在电极表面。之后,将电极与小鼠 IgG 的抗原孵育,然后与用 Ru-SiO(2)标记的二级抗体反应。因此,通过 Ru-SiO(2)和三丙胺(TPA)的 ECL 响应,获得了强的 ECL 信号,并实现了蛋白质相互作用的放大分析。该免疫传感器对检测小鼠 IgG 的线性范围为 0.05-200.00ng mL(-1),检测下限为 17pg mL(-1)。与其他类似研究相比,检测限提高了 4-300 倍。通过透射电子显微镜(TEM)对 Ru-SiO(2)纳米粒子的形貌进行了表征。通过循环伏安法(CV)研究了免疫传感器的制备过程,并通过电化学发光分析仪监测了免疫传感器的性能。这种制备 ECL 免疫传感器的新策略易于实现,具有在超灵敏生物分析中应用的潜力。