TY - JOUR
T1 - Rapid imaging and detection of circulating tumor cells using a wide-field fluorescence imaging system
AU - Yoshino, Tomoko
AU - Takai, Kaori
AU - Negishi, Ryo
AU - Saeki, Tatsuya
AU - Kanbara, Hisashige
AU - Kikuhara, Yoshihito
AU - Matsunaga, Tadashi
AU - Tanaka, Tsuyoshi
PY - 2017/5/29
Y1 - 2017/5/29
N2 - Circulating tumor cells (CTCs) provide potentially accessible in vivo sources of metastatic cancer cells. As such, considerable focus has been placed on analyzing the genetics of single-CTCs. Prior to these analyses, however, CTCs must first be detected within the blood samples of cancer patients. Current methods for detection of CTCs by fluorescence microscopy require the analysis of hundreds of images per blood sample, making this a time-consuming process that creates a bottleneck in CTC analysis. In this study, we therefore developed a wide-field fluorescence imaging system for rapid CTC detection. For these analyses, CTCs were first isolated using the microcavity array (MCA), a micro-sized filter for CTC recovery that separates cells based on differences in cell size and deformability. Notably, the proposed imaging system enabled rapid (∼10 s) visualization of all stained cells within the 6 mm × 6 mm MCA field via one-shot imaging. Furthermore, the morphology of the cells in the resulting images accurately reflected that observed by conventional microscopy. In total, isolation and detection of CTCs using the MCA combined with our novel wide-field fluorescence imaging system was achieved within 1 h. Thus, our proposed system will provide rapid CTC detection system.
AB - Circulating tumor cells (CTCs) provide potentially accessible in vivo sources of metastatic cancer cells. As such, considerable focus has been placed on analyzing the genetics of single-CTCs. Prior to these analyses, however, CTCs must first be detected within the blood samples of cancer patients. Current methods for detection of CTCs by fluorescence microscopy require the analysis of hundreds of images per blood sample, making this a time-consuming process that creates a bottleneck in CTC analysis. In this study, we therefore developed a wide-field fluorescence imaging system for rapid CTC detection. For these analyses, CTCs were first isolated using the microcavity array (MCA), a micro-sized filter for CTC recovery that separates cells based on differences in cell size and deformability. Notably, the proposed imaging system enabled rapid (∼10 s) visualization of all stained cells within the 6 mm × 6 mm MCA field via one-shot imaging. Furthermore, the morphology of the cells in the resulting images accurately reflected that observed by conventional microscopy. In total, isolation and detection of CTCs using the MCA combined with our novel wide-field fluorescence imaging system was achieved within 1 h. Thus, our proposed system will provide rapid CTC detection system.
KW - Circulating tumor cells
KW - CMOS sensor
KW - Fluorescence
KW - Microcavity array
KW - One shot imaging
KW - Wide-field imaging
UR - http://www.scopus.com/inward/record.url?scp=85016421647&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85016421647&partnerID=8YFLogxK
U2 - 10.1016/j.aca.2017.03.030
DO - 10.1016/j.aca.2017.03.030
M3 - Article
C2 - 28411625
AN - SCOPUS:85016421647
SN - 0003-2670
VL - 969
SP - 1
EP - 7
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
ER -