Key Laboratory of Luminescence and Real-Time Analysis (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Biosens Bioelectron. 2011 Sep 15;27(1):141-7. doi: 10.1016/j.bios.2011.06.031. Epub 2011 Jul 1.
A disposable electrochemiluminescent (ECL) immunosensor array was fabricated on a screen-printed carbon electrode (SPCE) substrate to perform multiplexed immunoassay (MIA) for the first time. The SPCE substrate was composed of an array of four carbon working electrodes, one common Ag/AgCl reference electrode, and one common carbon counter electrode. The immunosensor array was constructed by site-selectively immobilizing multiple antigens on different working electrodes of the SPCE substrate. With a competitive immunoassay format, the immobilized antigens competed with antigens in the sample to capture their corresponding tri(2,2'-bipyridyl)ruthenium(II)-labeled antibodies. The ECL signals from the immunosensors in this array were sequentially detected by a photomultiplier with the aid of a homemade single-pore-four-throw switch. Due to the ECL readout mechanism and the sequential detection mode, it could avoid the cross-talk between the adjacent immunosensors, which was common in other reported immunosensor array. Human, rabbit and mouse immunoglobulin Gs were near-simultaneously assayed as the model analytes. The linear ranges for them were 10-400, 20-400, and 20-400 ng/mL, with detection limits of 2.9, 6.1 and 6.5 ng/mL (S/N=3), respectively. This novel ECL strategy based on immunosensor array coupled with non-array detector provided a simple, sensitive, low-cost and time-saving approach for MIA. It showed great application potential in point-of-care test and field analysis of bio-agents, with mass production potential and high throughput.
一种一次性电化学发光(ECL)免疫传感器阵列被构建在丝网印刷碳电极(SPCE)基底上,首次实现了多重免疫分析(MIA)。SPCE 基底由四个碳工作电极、一个公共的 Ag/AgCl 参比电极和一个公共的碳对电极组成。免疫传感器阵列通过在 SPCE 基底的不同工作电极上选择性地固定多个抗原来构建。采用竞争免疫分析模式,固定的抗原与样品中的抗原竞争,以捕获它们相应的三(2,2'-联吡啶)钌(II)标记的抗体。通过光电倍增管,借助自制的单孔四掷开关,依次检测阵列中免疫传感器的 ECL 信号。由于 ECL 读出机制和顺序检测模式,可以避免相邻免疫传感器之间的串扰,这在其他报道的免疫传感器阵列中很常见。人、兔和鼠免疫球蛋白 G 被同时作为模型分析物进行检测。它们的线性范围分别为 10-400、20-400 和 20-400 ng/mL,检测限分别为 2.9、6.1 和 6.5 ng/mL(S/N=3)。这种基于免疫传感器阵列与非阵列检测器相结合的新型 ECL 策略为 MIA 提供了一种简单、灵敏、低成本和节省时间的方法。它在生物试剂的即时检测和现场分析中具有巨大的应用潜力,具有大规模生产和高通量的潜力。