State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Anal Chem. 2012 May 1;84(9):4207-13. doi: 10.1021/ac300551e. Epub 2012 Apr 18.
This paper describes a novel on-chip microarray platform based on an electrochemiluminescence resonance energy transfer (ECL-RET) strategy for rapid assay of cancer cell surface biomarkers. This platform consists of 64 antigen-decorated CdS nanorod spots with the diameter of 1.0 cm uniformly distributed on 16 indium tin oxide (ITO) strips, which is coated with a multichannel decorated polydimethylsiloxane (PDMS) slice to realize multiplexed determination of antigens. To shorten the immune reaction time in the microchannels and simplify the device, magnetic stirring and four-channel universal serial bus (USB) ports for plug-and-play were used. When Ru(bpy)(3)(2+) labeled antibodies were selectively captured by the corresponding antigens on the CdS nanorod spot array, ECL-RET from the CdS nanorod (donor) by cathodic emission in the presence of K(2)S(2)O(8) to Ru(bpy)(3)(2+) (acceptor) occurred. With signal amplification of Ru(bpy)(3)(2+) and competitive immunoassay, carcinoembryonic antigen (CEA), α-fetoprotein (AFP), and prostate specific antigen (PSA) as models were detected on this microfluidic device via recording the increased ECL-RET signals on electrode surfaces. Furthermore, this multiplexed competitive immunoassay was successfully used for detecting cancer cell surface antigens via the specific antibody-cell interactions and cell counting via cell surface receptors and antigens on the CdS nanorod surface. This platform provides a rapid and simple but sensitive approach with microliter-level sample volume and holds great promise for multiplexed detection of antigens and antigen-specific cells.
本文介绍了一种基于电致化学发光共振能量转移(ECL-RET)策略的新型片上微阵列平台,用于快速测定癌细胞表面标志物。该平台由 64 个均匀分布在 16 个铟锡氧化物(ITO)条上的直径为 1.0 厘米的抗原修饰的 CdS 纳米棒点组成,该平台涂有多通道修饰的聚二甲基硅氧烷(PDMS)片,以实现抗原的多重测定。为了缩短微通道中的免疫反应时间并简化设备,使用了磁搅拌和四通道通用串行总线(USB)端口,实现即插即用。当 Ru(bpy)(3)(2+)标记的抗体被 CdS 纳米棒点阵列上相应的抗原选择性捕获时,在存在 K(2)S(2)O(8)的情况下,从 CdS 纳米棒(供体)发生阴极发射的 ECL-RET 到 Ru(bpy)(3)(2+)(受体)。通过 Ru(bpy)(3)(2+)的信号放大和竞争免疫测定,以癌胚抗原(CEA)、α-胎蛋白(AFP)和前列腺特异性抗原(PSA)为模型,通过记录电极表面增加的 ECL-RET 信号,在该微流控装置上进行检测。此外,通过特异性抗体-细胞相互作用和通过 CdS 纳米棒表面的细胞表面受体和抗原进行细胞计数,成功地将这种多重竞争免疫测定用于检测癌细胞表面抗原。该平台提供了一种快速、简单但灵敏的方法,具有微升级别的样品量,有望用于抗原和抗原特异性细胞的多重检测。