Beyor Nathaniel, Seo Tae Seok, Liu Peng, Mathies Richard A
UCSF/UC Berkeley Joint Graduate Group in Bioengineering, University of California, Berkeley, CA, 94720, USA.
Department of Chemistry, University of California, Berkeley, CA, 94720, USA.
Biomed Microdevices. 2008 Dec;10(6):909. doi: 10.1007/s10544-008-9206-3.
A cell concentration microdevice for immunomagnetic pathogen isolation from a dilute sample is presented. Cells are driven by integrated on-chip pumps through a fluidized bed of immobilized immunomagnetic beads. Off-chip polymerase chain reaction and capillary electrophoretic analysis are used to determine capture efficiencies of E. coli and to optimize the system. Beads are immobilized after each split in a bifurcated channel system to ensure a balanced distribution of beads in all the capture channels. The addition of a pumping flutter step to repeatedly drive sample through the bead bed was found to enhance capture. Capture efficiencies of 70% and a limit of detection of 2 cfu/microL were achieved; specific capture of E. coli at a concentration of 100 cfu/microL in a 100-fold background of S. aureus is shown. This capture/concentration system is an important step in overcoming the macro-to-micro interface challenge in the development of microdevices for pathogen detection.
本文介绍了一种用于从稀释样品中免疫磁分离病原体的细胞浓度微器件。细胞由集成在芯片上的泵驱动,通过固定化免疫磁珠的流化床。芯片外聚合酶链反应和毛细管电泳分析用于确定大肠杆菌的捕获效率并优化系统。在分叉通道系统的每次分流后固定磁珠,以确保磁珠在所有捕获通道中均匀分布。发现添加泵送颤动步骤以反复驱动样品通过磁珠床可提高捕获率。实现了70%的捕获效率和2 cfu/μL的检测限;展示了在100倍金黄色葡萄球菌背景下对浓度为100 cfu/μL的大肠杆菌进行特异性捕获。这种捕获/浓缩系统是克服病原体检测微器件开发中宏观到微观界面挑战的重要一步。