Saraf Nileshi, Villegas Michael, Willenberg Bradley Jay, Seal Sudipta
Advanced Materials Processing and Analysis Centre, Department of Materials Science and Engineering, Department of Internal Medicine, College of Medicine, and Nanoscience Technology Centre, University of Central Florida, Orlando, Florida 32827, United States.
University of Florida, Gainesville, Florida 32611, United States.
ACS Omega. 2019 Jan 31;4(1):2234-2240. doi: 10.1021/acsomega.8b03277. Epub 2019 Jan 29.
A polydimethylsiloxane-based microfluidic device has been developed for the multiplex detection of viral envelope proteins such as Zika and chikungunya on a single platform using aptamer-analyte interactions. The channel is integrated with microsized pillars that increase the surface area allowing more aptamers to attach to the incoming envelope protein molecules, thus increasing the overall sensitivity of the system. The working of the device depends on the formation of protein-mediated sandwich morphology that is obtained using an aptamer and aptamer-functionalized gold nanoparticle (AuNP) pair. The colorimetric signal is obtained upon introduction of silver reagents into the channel, which are selectively deposited on the AuNP surface, providing a gray contrast in the testing zone. The microfluidic channel approach successfully detected clinically relevant concentrations of Zika and chikungunya envelope proteins in phosphine-buffered saline (1 pM) and calf blood (100 pM) with high specificity using gold-decorated aptamers integrated in a microfluidic channel.
一种基于聚二甲基硅氧烷的微流控装置已被开发出来,用于在单个平台上利用适体-分析物相互作用对寨卡病毒和基孔肯雅病毒等病毒包膜蛋白进行多重检测。该通道与微型柱集成在一起,增加了表面积,使更多适体能够附着到进入的包膜蛋白分子上,从而提高了系统的整体灵敏度。该装置的工作依赖于使用适体和适体功能化金纳米颗粒(AuNP)对形成的蛋白质介导的夹心形态。在将银试剂引入通道后获得比色信号,银试剂选择性地沉积在AuNP表面,在测试区域提供灰色对比度。微流控通道方法使用集成在微流控通道中的金修饰适体,成功地在磷酸缓冲盐水(1 pM)和小牛血液(100 pM)中以高特异性检测到临床相关浓度的寨卡病毒和基孔肯雅病毒包膜蛋白。