Biomicrofluidics. 2010 Sep 30;4(3):32207. doi: 10.1063/1.3437592.
Immunoassay is one of the important applications of microfluidic chips and many methodologies were reported for decreasing sample∕reagent volume, shortening assay time, and so on. Micro-enzyme-linked immunosorbent assay (micro-ELISA) is our method that utilizes packed microbeads in the microfluidic channel and the immunoreactions are induced on the beads surface. Due to the large surface-to-volume ratio and small analytical volume, excellent performances have been verified in assay time and sample∕reagent volume. In order to realize the micro-ELISA, one of the important processes is the immobilization of antibody on the beads surface. Previously, the immobilization process was performed in a macroscale tube by physisorption of antibody, and long time (2 h) and large amount of antibody (or high concentration) were required for the immobilization. In addition, the processes including the reaction and washing were laborious, and changing the analyte was not easy. In this research, we integrated the immobilization process into a microfluidic chip by applying the avidin-biotin surface chemistry. The integration enabled very fast (1 min) immobilization with very small amount of precious antibody consumption (100 ng) for one assay. Because the laborious immobilization process can be automatically performed on the microfluidic chip, ELISA method became very easy. On-demand immunoassay was also possible just by changing the antibodies without using large amount of precious antibodies. Finally, the analytical performance was investigated by measuring C-reactive protein and good performance (limit of detection <20 ng∕ml) was verified.
免疫测定是微流控芯片的重要应用之一,已经有许多方法被报道用于减少样品/试剂的体积、缩短测定时间等。微酶联免疫吸附测定(micro-ELISA)是我们的方法,它利用微流道中的包被微珠,并在珠表面诱导免疫反应。由于大的表面积/体积比和小的分析体积,在测定时间和样品/试剂体积方面已经验证了优异的性能。为了实现 micro-ELISA,其中一个重要的过程是抗体在珠表面的固定化。以前,抗体的固定化过程是在宏观试管中通过物理吸附来进行的,并且需要较长的时间(2 小时)和大量的抗体(或高浓度)来进行固定化。此外,包括反应和洗涤在内的过程都很繁琐,并且改变分析物也不容易。在这项研究中,我们通过应用亲和素-生物素表面化学将固定化过程集成到微流控芯片中。这种集成使得非常快速(1 分钟)的固定化,并且仅需非常少量的昂贵抗体(100ng)即可进行一次测定。由于费力的固定化过程可以在微流控芯片上自动进行,ELISA 方法变得非常简单。只需更换抗体而无需使用大量昂贵的抗体,即可实现按需免疫测定。最后,通过测量 C 反应蛋白来研究分析性能,并验证了良好的性能(检测限<20ng/ml)。