Bi Sai, Yan Yameng, Yang Xiaoyan, Zhang Shusheng
Key Laboratory of Eco-chemical Engineering, Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, China.
Chemistry. 2009;15(18):4704-9. doi: 10.1002/chem.200801722.
Gold'n'beads: A chemiluminescence immunoassay for the sensitive and rapid determination of AFP has been developed, employing bromophenol blue as a novel chemiluminescence enhancer by taking advantages of easy separation by magnetic beads and signal amplification by gold nanoparticles based on a sandwich-type immunoreaction (see scheme).A novel and sensitive chemiluminescence immunoassay (CLIA) has been developed by employing a new chemiluminescence (CL) enhancer, bromophenol blue (BPB), for the determination of alpha-fetoprotein (AFP) based on magnetic beads (MBs) and colloidal gold nanoparticles (AuNPs) modified with HRP-labeled anti-AFP antibodies. BPB, as a chemical indicator, was found to act as a novel and highly signal enhancer of the peroxidase-catalyzed CL reaction of luminol with hydrogen peroxide. After optimizing the CL reaction conditions, this new luminol-H(2)O(2)-HRP-BPB CL system was applied to a sandwich-type CLIA based on the magnetic separation and the amplification feature of AuNPs as HRP labels. A linear range was obtained when the concentrations of AFP were from 0.1 to 5.0 ng mL(-1) (R=0.9997) with the detection limit of 0.01 ng mL(-1) (3sigma), which is one order of magnitude lower than that obtained without using AuNPs, and much lower than that typically achieved by ELISA. The present method was successfully applied to the determination of AFP in human serum samples. The results indicated that this proposed protocol could be quite promising for the application in immunoassays.
开发了一种用于灵敏快速测定甲胎蛋白(AFP)的化学发光免疫分析法,该方法利用溴酚蓝作为新型化学发光增强剂,基于夹心型免疫反应,借助磁珠实现易于分离,并通过金纳米颗粒实现信号放大(见示意图)。通过采用新型化学发光(CL)增强剂溴酚蓝(BPB),基于用辣根过氧化物酶(HRP)标记的抗AFP抗体修饰的磁珠(MBs)和胶体金纳米颗粒(AuNPs),开发了一种新型灵敏的化学发光免疫分析法(CLIA)用于测定甲胎蛋白(AFP)。发现作为化学指示剂的BPB可作为鲁米诺与过氧化氢的过氧化物酶催化CL反应的新型高效信号增强剂。优化CL反应条件后,将这种新的鲁米诺-H₂O₂-HRP-BPB CL体系应用于基于磁分离和AuNPs作为HRP标记的放大特性的夹心型CLIA。当AFP浓度为0.1至5.0 ng mL⁻¹时获得线性范围(R = 0.9997),检测限为0.01 ng mL⁻¹(3σ),这比不使用AuNPs时获得的检测限低一个数量级,且远低于酶联免疫吸附测定(ELISA)通常达到的检测限。本方法成功应用于人血清样品中AFP的测定。结果表明,该方法在免疫分析中的应用前景广阔。