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基于电致化学发光共振能量转移的用于细胞表面抗原的多重免疫分析的带有 64 位电极阵列的微芯片器件。

Microchip device with 64-site electrode array for multiplexed immunoassay of cell surface antigens based on electrochemiluminescence resonance energy transfer.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.

出版信息

Anal Chem. 2012 May 1;84(9):4207-13. doi: 10.1021/ac300551e. Epub 2012 Apr 18.

Abstract

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.

摘要

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。

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