Wang Ying-Chih, Han Jongyoon
Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Lab Chip. 2008 Mar;8(3):392-4. doi: 10.1039/b717220f. Epub 2008 Jan 14.
Almost all immuno-biosensors are inherently limited by the quality of antibodies available for the target molecule, and obtaining a highly sensitive antibody for a given target molecule is a challenge. We describe a highly efficient and flexible way to enhance immunoassay detection sensitivity and binding kinetics using a nanofluidic based electrokinetic preconcentrator. The device is a microfluidic integration of charge-based biomolecule concentrator and a bead-based immunoassay. Because the preconcentrator can increase the local biomolecule concentration by many orders of magnitude, it gives the immuno-sensor better sensitivity and faster binding kinetics. With a 30 min preconcentration, we were able to enhance the immunoassay sensitivity (with molecular background) by more than 500 fold from higher 50 pM to the sub 100 fM range. Moreover, by adjusting the preconcentration time, we can switch the detection range of the given bead-based assay (from 10-10 000 ng ml(-1) to 0.01-10 000 ng ml(-1)) to have a broader dynamic range of detection. As the system can enhance both detection sensitivity and dynamic range, it can be used to address the most critical detection issues in the detection of common disease biomarkers.
几乎所有免疫生物传感器本质上都受到针对目标分子可用抗体质量的限制,而获得针对给定目标分子的高灵敏度抗体是一项挑战。我们描述了一种高效且灵活的方法,即使用基于纳米流体的电动预浓缩器来提高免疫分析检测灵敏度和结合动力学。该设备是基于电荷的生物分子浓缩器与基于微珠的免疫分析的微流体集成。由于预浓缩器可以将局部生物分子浓度提高多个数量级,因此它能使免疫传感器具有更好的灵敏度和更快的结合动力学。经过30分钟的预浓缩,我们能够将免疫分析灵敏度(有分子背景)从高于50 pM提高到低于100 fM范围,提高了500多倍。此外,通过调整预浓缩时间,我们可以切换给定基于微珠分析的检测范围(从10 - 10000 ng ml(-1)到0.01 - 10000 ng ml(-1)),以获得更宽的动态检测范围。由于该系统可以提高检测灵敏度和动态范围,它可用于解决常见疾病生物标志物检测中最关键的检测问题。