TY - GEN
T1 - Membrane sieve using stoichiometric and stress-reduced SiN/SiO/SiN multilayer films and applications to plasma separation
AU - Lee, Dae Sik
AU - Choi, Yo Han
AU - Jun, Mun Yeon
AU - Han, Yong Duk
AU - Yoon, Hyun C.
AU - Shoji, Shuichi
PY - 2012/12/1
Y1 - 2012/12/1
N2 - We have proposed a stoichiometric and stress-reduced silicon nitride/silicon oxide/silicon nitride (N/O/N) triple-layer membrane sieves. The membrane sieves were designed to be ultra flat and thin, mechanically stress-reduced, and stable in their electrical and chemical properties. All insulating materials are deposited stoichiometrically by a low pressure chemical vapor deposition (LPCVD) system. The SiN/SiO/SiN membranes with a thickness of 0.4 mm have pores with diameters of 0.6-2 mm. The device is easily fabricated on a 6' silicon wafer with full compatibility with CMOS processes. To see the separation ability of blood plasma, an agarose gel matrix was attached to the sieves for improving the speed, which can be delayed by clogging. We could separate about 1 mL of plasma from 5 mL of human whole blood. We believes that our device can be applicable for the cell-based biosensors or analysis systems in analytical chemistry and bioseparation system.
AB - We have proposed a stoichiometric and stress-reduced silicon nitride/silicon oxide/silicon nitride (N/O/N) triple-layer membrane sieves. The membrane sieves were designed to be ultra flat and thin, mechanically stress-reduced, and stable in their electrical and chemical properties. All insulating materials are deposited stoichiometrically by a low pressure chemical vapor deposition (LPCVD) system. The SiN/SiO/SiN membranes with a thickness of 0.4 mm have pores with diameters of 0.6-2 mm. The device is easily fabricated on a 6' silicon wafer with full compatibility with CMOS processes. To see the separation ability of blood plasma, an agarose gel matrix was attached to the sieves for improving the speed, which can be delayed by clogging. We could separate about 1 mL of plasma from 5 mL of human whole blood. We believes that our device can be applicable for the cell-based biosensors or analysis systems in analytical chemistry and bioseparation system.
UR - http://www.scopus.com/inward/record.url?scp=84873942430&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84873942430&partnerID=8YFLogxK
U2 - 10.1109/ICSENS.2012.6411404
DO - 10.1109/ICSENS.2012.6411404
M3 - Conference contribution
AN - SCOPUS:84873942430
SN - 9781457717659
T3 - Proceedings of IEEE Sensors
BT - IEEE SENSORS 2012 - Proceedings
T2 - 11th IEEE SENSORS 2012 Conference
Y2 - 28 October 2012 through 31 October 2012
ER -