TY - JOUR
T1 - On-chip cell sorting system using thermoreversible gelation polymer
AU - Shirasaki, Yoshitaka
AU - Sugino, Hirokazu
AU - Tatsuoka, Masayasu
AU - Mizuno, Jun
AU - Shoji, Shuichi
AU - Funatsu, Takashi
N1 - Funding Information:
Manuscript received October 2, 2006; accepted February 13, 2007. This work was supported in part by Mitsubishi Foundation, SENTAN, Japan Science and Technology (JST), and in part by the Grants-in-Aid for Specially Promoted Research, Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan under Grant (A) 12450167.
PY - 2007/3
Y1 - 2007/3
N2 - We have developed a microfabricated fluorescence-activated cell sorter system using laminar flow of thermoreversible gelation polymer (TGP). The glass sorter chip consists of microchannels with two inlets for sample and buffer solutions, and two outlets for collection and waste of the specimen. A biological specimen containing fluorescently labeled cells, is mixed with a solution containing a TGP. The laminar flow of the mixed solution and buffer solution are then introduced into the sorter chip. The fluorescently labeled target cells were detected with sensitive fluorescence microscopy. In the absence of a fluorescence signal, the laminar flow of the specimen is directed into the waste channel. Upon detection of a fluorescence signal from the target cells, the sol-gel transformation was locally induced by site-directed infrared laser irradiation for the flow switching and for allowing the fluorescent cells to be channeled into the collection reservoir. The flow switching time of 100 ms was achieved. Using this system, we have demonstrated the sorting of Escherichia call cells expressing fluorescent proteins. These cells were found to be viable after extraction from the sorting system, indicating no damage to the cells.
AB - We have developed a microfabricated fluorescence-activated cell sorter system using laminar flow of thermoreversible gelation polymer (TGP). The glass sorter chip consists of microchannels with two inlets for sample and buffer solutions, and two outlets for collection and waste of the specimen. A biological specimen containing fluorescently labeled cells, is mixed with a solution containing a TGP. The laminar flow of the mixed solution and buffer solution are then introduced into the sorter chip. The fluorescently labeled target cells were detected with sensitive fluorescence microscopy. In the absence of a fluorescence signal, the laminar flow of the specimen is directed into the waste channel. Upon detection of a fluorescence signal from the target cells, the sol-gel transformation was locally induced by site-directed infrared laser irradiation for the flow switching and for allowing the fluorescent cells to be channeled into the collection reservoir. The flow switching time of 100 ms was achieved. Using this system, we have demonstrated the sorting of Escherichia call cells expressing fluorescent proteins. These cells were found to be viable after extraction from the sorting system, indicating no damage to the cells.
KW - Cell sorter
KW - Flow cytometry
KW - Microsystem
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U2 - 10.1109/JSTQE.2007.894052
DO - 10.1109/JSTQE.2007.894052
M3 - Article
AN - SCOPUS:34247474912
SN - 1077-260X
VL - 13
SP - 223
EP - 227
JO - IEEE Journal of Selected Topics in Quantum Electronics
JF - IEEE Journal of Selected Topics in Quantum Electronics
IS - 2
ER -