Department of Chemistry (U-3060), University of Connecticut, 55 North Eagleville Road, Storrs, Connecticut 06269, USA.
Anal Chem. 2011 Sep 1;83(17):6698-703. doi: 10.1021/ac201292q. Epub 2011 Jul 29.
This paper describes fabrication of a novel electrochemiluminescence (ECL) immunosensor array featuring capture-antibody-decorated single-wall carbon nanotube (SWCNT) forests residing in the bottoms of 10-μL wells with hydrophobic polymer walls. Silica nanoparticles containing Ru(bpy)(3) and secondary antibodies (RuBPY-silica-Ab(2)) are employed in this system for highly sensitive two-analyte detection. Antibodies to prostate specific antigen (PSA) and interleukin-6 (IL-6) were attached to the same RuBPY-silica-Ab(2) particle. The array was fabricated by forming the wells on a conductive pyrolytic graphite chip (1 in. × 1 in.) with a single connection to a potentiostat to achieve ECL. The sandwich immunoassay protocol employs antibodies attached to SWCNTs in the wells to capture analyte proteins. Then RuBPY-silica-Ab(2) is added to bind to the captured proteins. ECL is initiated in the microwells by electrochemical oxidation of tripropyl amine (TprA), which generates excited state Ru(bpy)(3) in the 100-nm particles, and is measured with a charge-coupled device (CCD) camera. Separation of the analytical spots by the hydrophobic wall barriers enabled simultaneous immunoassays for two proteins in a single sample without cross-contamination. The detection limit (DL) for PSA was 1 pg mL(-1) and for IL-6 was 0.25 pg mL(-1) (IL-6) in serum. Array determinations of PSA and IL-6 in patient serum were well-correlated with single-protein ELISAs. These microwell SWCNT immunoarrays provide a simple, sensitive approach to the detection of two or more proteins.
本文描述了一种新型电化学发光(ECL)免疫传感器阵列的制作方法,该阵列具有独特的特点,即在具有疏水聚合物壁的 10μL 小室底部,捕获抗体修饰的单壁碳纳米管(SWCNT)森林。该系统采用含有 Ru(bpy)(3)和二级抗体(RuBPY-二氧化硅-Ab(2))的纳米硅颗粒,用于高灵敏度的双分析物检测。针对前列腺特异性抗原(PSA)和白细胞介素-6(IL-6)的抗体被连接到相同的 RuBPY-二氧化硅-Ab(2)颗粒上。该阵列是通过在导电热解石墨芯片(1 英寸×1 英寸)上形成小室,并与一个电化学工作站进行单一连接来实现 ECL 进行制作的。三明治免疫分析方案采用附着在小室 SWCNT 上的抗体来捕获分析物蛋白。然后加入 RuBPY-二氧化硅-Ab(2)与捕获的蛋白质结合。通过电化学氧化三丙胺(TprA)在微室中引发 ECL,在 100nm 颗粒中生成激发态 Ru(bpy)(3),并用电荷耦合器件(CCD)相机进行测量。通过疏水壁障将分析点分离,可在单个样品中同时进行两种蛋白质的免疫分析,而不会发生交叉污染。在血清中,PSA 的检测限(DL)为 1pg mL(-1),IL-6 的检测限(DL)为 0.25pg mL(-1)。对患者血清中 PSA 和 IL-6 的阵列测定与单蛋白 ELISA 相关性良好。这些微室 SWCNT 免疫阵列为检测两种或更多种蛋白质提供了一种简单、灵敏的方法。