TY - GEN
T1 - Post-CMOS packaging methods for integrated biosensors
AU - Dandin, Marc
AU - Jung, Im Deok
AU - Piyasena, Menake
AU - Gallagher, James
AU - Nelson, Nicole
AU - Urdaneta, Mario
AU - Artis, Chantelle
AU - Abshire, Pamela
AU - Smela, Elisabeth
PY - 2009
Y1 - 2009
N2 - We report on several techniques that have been pursued in our laboratories for packaging complementary metal-oxide semiconductor (CMOS) sensors for use in biological environments, such as cell medium. These techniques are suited for single CMOS die ranging from 1.5 x 1.5 mm2 to 3 x 3 mm2 in area. The first method consisted of creating high aspect ratio structures from negative-tone photocurable resins to simultaneously encapsulate wirebonds from the chip to a ceramic package and create a cell culture well. The second technique used a photolithographically defined barrier on the die to allow the use of non-photocurable resins as encapsulants. The third method consisted of re-routing the die padframe using photolithographically defined, planar leads to a much larger padframe; this will allow the chip to be integrated with microfluidic networks. Finally, we show a method in which the encapsulant was also used as an optical filter and as a base for integrating more complex structures.
AB - We report on several techniques that have been pursued in our laboratories for packaging complementary metal-oxide semiconductor (CMOS) sensors for use in biological environments, such as cell medium. These techniques are suited for single CMOS die ranging from 1.5 x 1.5 mm2 to 3 x 3 mm2 in area. The first method consisted of creating high aspect ratio structures from negative-tone photocurable resins to simultaneously encapsulate wirebonds from the chip to a ceramic package and create a cell culture well. The second technique used a photolithographically defined barrier on the die to allow the use of non-photocurable resins as encapsulants. The third method consisted of re-routing the die padframe using photolithographically defined, planar leads to a much larger padframe; this will allow the chip to be integrated with microfluidic networks. Finally, we show a method in which the encapsulant was also used as an optical filter and as a base for integrating more complex structures.
UR - https://www.scopus.com/pages/publications/77951117738
U2 - 10.1109/ICSENS.2009.5398540
DO - 10.1109/ICSENS.2009.5398540
M3 - Conference contribution
AN - SCOPUS:77951117738
SN - 9781424445486
T3 - Proceedings of IEEE Sensors
SP - 795
EP - 798
BT - IEEE Sensors 2009 Conference - SENSORS 2009
T2 - IEEE Sensors 2009 Conference - SENSORS 2009
Y2 - 25 October 2009 through 28 October 2009
ER -