Single cell level detection of Escherichia coli in microfluidic device

被引:39
作者
Han, Jin-Hee [1 ]
Heinze, Brian C. [1 ]
Yoon, Jeong-Yeol [1 ]
机构
[1] Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ 85721 USA
基金
美国国家科学基金会;
关键词
Escherichia coli K-12; proximity optical fiber; latex immunoagglutination assay; latex agglutination test; microfluidic device; detection limit; static light scattering;
D O I
10.1016/j.bios.2007.11.013
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Detection of Escherichia coli K-12 in phosphate buffered saline (PBS) was demonstrated in a Y-channel polydimethylsitoxane (PDMS) microfluidic device! through optical fiber monitoring of latex immunoagglutination. The latex immunoagglutination assay was performed for serially diluted E. coli solutions using 0.92-mu m highly carboxylated polystyrene particles conjugated with polyclonal anti-E. coli. Pre-treatments such as cell lysis or culturing to enhance the signal were not used. Proximity optical fibers around the view cell of the device were used to quantify the increase in 45 degrees forward light scattering of the immunoagglutinated particles. In order to reduce false positive signals caused by antibodies binding to non-viable E. coli cells or free antigens in solution, target solutions were washed three times, and then the results were compared to non-washing treatments. The detection limit was found to be less than 10 cfu ml(-1) (1 cfu per device) without PBS washing (thus detecting non-viable cells and free antigens), or less than 40 cfu ml(-1) (4 cfu per device) with PBS washing (thus detecting viable E. coli cells only). (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1303 / 1306
页数:4
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