TY - GEN
T1 - Integrated PDMS/CMOS microsystem for autonomous incubation and imaging in cell culture studies
AU - Blain Christen, Jennifer M.
AU - Andreou, Andreas G.
PY - 2006
Y1 - 2006
N2 - We discuss the design, fabrication and testing of a hybrid microsystem for stand-alone cell culture, incubation and imaging. The micro-incubator is engineered through the integration of two CMOS dies. The first for the heater and temperature sensor, and a second die for imaging. A multilayer PDMS (polydimethylsiloxane) structures is used to create not only the fluidic structures but to encapsulate the CMOS dies. The microfluidic features include fluidic channels, a 4mm diameter, 30μL, culture well and a 25 micron thick PDMS membrane that covers the top of the culture well, acting as barrier to contaminants while allowing the cells to exchange gases with the ambient environment. The micro-incubator interface includes with a flexible polyimide ribbon cable and four fluidic ports. The complete structure has a size of (2.5×2.5×0.6cm3). We have employed the device to successfully culture BHK-21 cells autonomously over a sixty hour period in ambient environment.
AB - We discuss the design, fabrication and testing of a hybrid microsystem for stand-alone cell culture, incubation and imaging. The micro-incubator is engineered through the integration of two CMOS dies. The first for the heater and temperature sensor, and a second die for imaging. A multilayer PDMS (polydimethylsiloxane) structures is used to create not only the fluidic structures but to encapsulate the CMOS dies. The microfluidic features include fluidic channels, a 4mm diameter, 30μL, culture well and a 25 micron thick PDMS membrane that covers the top of the culture well, acting as barrier to contaminants while allowing the cells to exchange gases with the ambient environment. The micro-incubator interface includes with a flexible polyimide ribbon cable and four fluidic ports. The complete structure has a size of (2.5×2.5×0.6cm3). We have employed the device to successfully culture BHK-21 cells autonomously over a sixty hour period in ambient environment.
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U2 - 10.1109/LSSA.2006.250430
DO - 10.1109/LSSA.2006.250430
M3 - Conference contribution
AN - SCOPUS:37649026755
SN - 1424402786
SN - 9781424402786
T3 - 2006 IEEE/NLM Life Science Systems and Applications Workshop, LiSA 2006
BT - 2006 IEEE/NLM Life Science Systems and Applications Workshop, LiSA 2006
T2 - 2006 IEEE/NLM Life Science Systems and Applications Workshop, LiSA 2006
Y2 - 13 July 2006 through 14 July 2006
ER -