On-chip cell sorting system using laser-induced heating of a thermoreversible gelation polymer to control flow

被引:57
作者
Shirasaki, Y
Tanaka, J
Makazu, H
Tashiro, K
Shoji, S
Tsukita, S
Funatsu, T
机构
[1] Waseda Univ, Sch Sci & Engn, Dept Phys, Shinjuku Ku, Tokyo 1698555, Japan
[2] Waseda Univ, Sch Sci & Engn, Dept Elect Engn & Biosci, Shinjuku Ku, Tokyo 1698555, Japan
[3] Kyoto Univ, Fac Med, Dept Cell Biol, Sakyo Ku, Kyoto 6068501, Japan
[4] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Bioanalyt Chem, Bunkyo Ku, Tokyo 1130033, Japan
关键词
D O I
10.1021/ac0511041
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed a microfabricated fluorescence-activated cell sorter system using a thermoreversible gelation polymer (TGP) as a switching valve. The glass sorter chip has Y-shaped microchannels with one inlet and two outlets. A biological specimen containing fluorescently labeled cells is mixed with a solution containing a thermoreversible sol-gel polymer. The mixed solution is then introduced into the sorter chip through the inlet. The sol-gel transformation was locally induced by site-directed infrared laser irradiation to plug one of the outlets. The fluorescently labeled target cells were detected with sensitive fluorescence microscopy. In the absence of a fluorescence signal, the collection channel is plugged through laser irradiation of the TGP and the specimens are directed to the waste channel. Upon detection of a fluorescence signal from the target cells, the laser beam is then used to plug the waste channel, allowing the fluorescent cells to be channeled into the collection reservoir. The response time of the sol-gel transformation was 3 ms, and a flow switching time of 120 ms was achieved. Using this system, we have demonstrated the sorting of fluorescent microspheres and Escherichia coli cells expressing fluorescent proteins. These cells were found to be viable after extraction from the sorting system, indicating no damage to the cells.
引用
收藏
页码:695 / 701
页数:7
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