Beyor Nathaniel, Yi Lina, Seo Tae Seok, Mathies Richard A
UCSF/UC Berkeley Joint Graduate Group in Bioengineering, University of California, Berkeley, California 94720, USA.
Anal Chem. 2009 May 1;81(9):3523-8. doi: 10.1021/ac900060r.
A laboratory-on-a-chip system for pathogen detection is presented that integrates cell preconcentration, purification, polymerase chain reaction (PCR), and capillary electrophoretic (CE) analysis. The microdevice is composed of micropumps and valves, a cell capture structure, a 100 nL PCR reactor, and a 5 cm long CE column for amplicon separation. Sample volumes ranging from 10 to 100 microL are introduced and driven through a fluidized bed of magnetically constrained immunomagnetic beads where the target cells are captured. After cell capture, beads are transferred using the on-chip pumps to the PCR reactor for DNA amplification. The resulting PCR products are electrophoretically injected onto the CE column for separation and detection of Escherichia coli K12 and E. coli O157 targets. A detection limit of 0.2 cfu/microL is achieved using the E. coli O157 target and an input volume of 50 microL. Finally, the sensitive detection of E. coli O157 in the presence of K12 at a ratio of 1:1000 illustrates the capability of our system to identify target cells in a high commensal background. This cell capture-PCR-CE microsystem is a significant advance in the development of rapid, sensitive, and specific laboratory-on-a-chip devices for pathogen detection.
本文介绍了一种用于病原体检测的芯片实验室系统,该系统集成了细胞预浓缩、纯化、聚合酶链反应(PCR)和毛细管电泳(CE)分析功能。该微型设备由微泵和阀门、细胞捕获结构、100 nL 的 PCR 反应器以及用于扩增子分离的 5 cm 长的 CE 柱组成。引入体积范围为 10 至 100 μL 的样品,并驱动其通过由磁性约束免疫磁珠组成的流化床,在该流化床中捕获目标细胞。细胞捕获后,使用芯片上的泵将磁珠转移到 PCR 反应器中进行 DNA 扩增。所得的 PCR 产物通过电泳注入到 CE 柱中,用于分离和检测大肠杆菌 K12 和大肠杆菌 O157 目标。使用大肠杆菌 O157 目标和 50 μL 的输入体积,实现了 0.2 cfu/μL 的检测限。最后,在 K12 存在的情况下以 1:1000 的比例对大肠杆菌 O157 进行灵敏检测,说明了我们的系统在高共生背景下识别目标细胞的能力。这种细胞捕获 - PCR - CE 微系统是用于病原体检测的快速、灵敏和特异性芯片实验室设备开发方面的一项重大进展。