The State Key Laboratory Base of Novel Functional Materials and Preparation Science, Faculty of Material Science and Chemical Engineering of Ningbo University, Ningbo 315211, China.
Anal Chim Acta. 2012 Oct 9;746:107-13. doi: 10.1016/j.aca.2012.08.036. Epub 2012 Aug 28.
A novel and sensitive sandwich-type electrochemiluminescence (ECL) immunosensor was fabricated on a glassy carbon electrode (GCE) for ultra trace levels of α-fetoprotein (AFP) based on sandwich immunoreaction strategy by enrichment using magnetic capture probes and quantum dots coated with Au shell (CdS-Au) as the signal tag. The capture probe was prepared by immobilizing the primary antibody of AFP (Ab1) on the core/shell Fe(3)O(4)-Au nanoparticles, which was first employed to capture AFP antigens to form Fe(3)O(4)-Au/Ab1/AFP complex from the serum after incubation. The product can be separated from the background solution through the magnetic separation. Then the CdS-Au labeled secondary antibody (Ab2) as signal tag (CdS-Au/Ab2) was conjugated successfully with Fe(3)O(4)-Au/Ab1/AFP complex to form a sandwich-type immunocomplex (Fe(3)O(4)-Au/Ab1/AFP/Ab2/CdS-Au), which can be further separated by an external magnetic field and produce ECL signals at a fixed voltage. The signal was proportional to a certain concentration range of AFP for quantification. Thus, an easy-to-use immunosensor with magnetic probes and a quantum dots signal tag was obtained. The immunosensor performed at a level of high sensitivity and a broad concentration range for AFP between 0.0005 and 5.0 ng mL(-1) with a detection limit of 0.2 pg mL(-1). The use of magnetic probes was combined with pre-concentration and separation for trace levels of tumor markers in the serum. Due to the amplification of the signal tag, the immunosensor is highly sensitive, which can offer great promise for rapid, simple, selective and cost-effective detection of effective biomonitoring for clinical application.
一种新型灵敏的夹心型电化学发光(ECL)免疫传感器在玻碳电极(GCE)上构建,基于夹心免疫反应策略,通过使用磁性捕获探针和量子点(CdS-Au)富集,作为信号标记物,用于超痕量水平的甲胎蛋白(AFP)检测。捕获探针通过将 AFP 的一级抗体(Ab1)固定在核/壳 Fe3O4-Au 纳米粒子上制备,该纳米粒子首先用于从孵育后的血清中捕获 AFP 抗原,形成 Fe3O4-Au/Ab1/AFP 复合物。通过磁性分离,可以将产物与背景溶液分离。然后,CdS-Au 标记的二级抗体(Ab2)作为信号标记物(CdS-Au/Ab2)与 Fe3O4-Au/Ab1/AFP 复合物成功缀合,形成夹心型免疫复合物(Fe3O4-Au/Ab1/AFP/Ab2/CdS-Au),可以通过外部磁场进一步分离,并在固定电压下产生 ECL 信号。信号与 AFP 的一定浓度范围内呈正比,用于定量。因此,获得了一种具有磁性探针和量子点信号标记物的易用型免疫传感器。该免疫传感器在 AFP 浓度为 0.0005 至 5.0 ng mL-1 的较宽范围内表现出高灵敏度,检测限为 0.2 pg mL-1。磁性探针的使用结合了痕量肿瘤标志物在血清中的预浓缩和分离。由于信号标记物的放大,该免疫传感器具有高灵敏度,为临床应用中快速、简单、选择性和具有成本效益的有效生物监测提供了很大的前景。