Choi Seokheun, Goryll Michael, Sin Lai Yi Mandy, Wong Pak Kin, Chae Junseok
1School of Electrical, Computer and Energy Engineering, Arizona State University, Tempe, AZ 85287 USA.
2Department of Aerospace and Mechanical Engineering, University of Arizona, Tucson, AZ 85721 USA.
Microfluid Nanofluidics. 2011;10(2):231-247. doi: 10.1007/s10404-010-0638-8. Epub 2010 Jun 2.
This article reviews state-of-the-art microfluidic biosensors of nucleic acids and proteins for point-of-care (POC) diagnostics. Microfluidics is capable of analyzing small sample volumes (10-10 l) and minimizing costly reagent consumption as well as automating sample preparation and reducing processing time. The merger of microfluidics and advanced biosensor technologies offers new promises for POC diagnostics, including high-throughput analysis, portability and disposability. However, this merger also imposes technological challenges on biosensors, such as high sensitivity and selectivity requirements with sample volumes orders of magnitude smaller than those of conventional practices, false response errors due to non-specific adsorption, and integrability with other necessary modules. There have been many prior review articles on microfluidic-based biosensors, and this review focuses on the recent progress in last 5 years. Herein, we review general technologies of DNA and protein biosensors. Then, recent advances on the coupling of the biosensors to microfluidics are highlighted. Finally, we discuss the key challenges and potential solutions for transforming microfluidic biosensors into POC diagnostic applications.
本文综述了用于即时检测(POC)诊断的核酸和蛋白质微流控生物传感器的最新技术。微流控技术能够分析少量样本(10 - 10升),最大限度地减少昂贵试剂的消耗,实现样本制备自动化并缩短处理时间。微流控技术与先进生物传感器技术的融合为即时检测诊断带来了新的前景,包括高通量分析、便携性和一次性使用。然而,这种融合也给生物传感器带来了技术挑战,例如对灵敏度和选择性的要求很高,因为样本体积比传统方法小几个数量级,非特异性吸附会导致错误响应误差,以及与其他必要模块的可集成性。此前已有许多关于基于微流控的生物传感器的综述文章,本综述聚焦于过去5年的最新进展。在此,我们综述了DNA和蛋白质生物传感器的一般技术。然后,重点介绍了生物传感器与微流控技术耦合的最新进展。最后,我们讨论了将微流控生物传感器转化为即时检测诊断应用的关键挑战和潜在解决方案。