TY - GEN
T1 - Integrated microfluidic probes for cell manipulation and analysis
AU - Brimmo, Ayoola
AU - Glia, Ayoub
AU - Sukumar, Pavithra
AU - Alnemari, Roaa
AU - Menachery, Anoop
AU - Deliorman, Muhammedin
AU - Qasaimeh, Mohammad A.
N1 - Publisher Copyright:
© COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.
PY - 2019
Y1 - 2019
N2 - The microfluidic probe (MFP) is a non-contact technology that applies the concept of hydrodynamic flow confinement within a small gap to eliminate the need for closed conduits, and thus overcomes the conventional microfluidic "closed system" limitations. It is an open-space microfluidic concept, where the fluidic delivery mechanism is physically decoupled from the target surface to be processed such as tissue slices or cell culture in Petri dishes. Typically, MFPs are manufactured using complex photolithography-based microfabrication procedures that limits innovation in MFPs' design and integration. Recently, we showed that 3D printing can be utilized for rapid microfabrication of MFPs, where MFPs can be manufactured with built-in components such as reservoirs, fluidic connectors, and interfaces to the XYZ probe holder. 3D printing brings flexibility in MFP design, where different configurations and aperture arrangements can be considered. Currently, we are developing advanced MFPs that are integrated with other technologies and targeting applications in dielectrophoretic-based cell separation, immuno-based cell capture for isolating circulating tumor cells from blood samples, and efficient and selective single cell electroporation. In this invited paper, we highlight several MFP technologies we are developing.
AB - The microfluidic probe (MFP) is a non-contact technology that applies the concept of hydrodynamic flow confinement within a small gap to eliminate the need for closed conduits, and thus overcomes the conventional microfluidic "closed system" limitations. It is an open-space microfluidic concept, where the fluidic delivery mechanism is physically decoupled from the target surface to be processed such as tissue slices or cell culture in Petri dishes. Typically, MFPs are manufactured using complex photolithography-based microfabrication procedures that limits innovation in MFPs' design and integration. Recently, we showed that 3D printing can be utilized for rapid microfabrication of MFPs, where MFPs can be manufactured with built-in components such as reservoirs, fluidic connectors, and interfaces to the XYZ probe holder. 3D printing brings flexibility in MFP design, where different configurations and aperture arrangements can be considered. Currently, we are developing advanced MFPs that are integrated with other technologies and targeting applications in dielectrophoretic-based cell separation, immuno-based cell capture for isolating circulating tumor cells from blood samples, and efficient and selective single cell electroporation. In this invited paper, we highlight several MFP technologies we are developing.
KW - 3D printing
KW - Concentration gradient
KW - Dielectrophoresis
KW - Electroporation
KW - Herringbone micro-mixers
KW - Micro electrodes
KW - Microfluidic probe
KW - Microfluidic quadrupole
UR - http://www.scopus.com/inward/record.url?scp=85066631600&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85066631600&partnerID=8YFLogxK
U2 - 10.1117/12.2515270
DO - 10.1117/12.2515270
M3 - Conference contribution
AN - SCOPUS:85066631600
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Microfluidics, BioMEMS, and Medical Microsystems XVII
A2 - Gray, Bonnie L.
A2 - Becker, Holger
PB - SPIE
T2 - Microfluidics, BioMEMS, and Medical Microsystems XVII 2019
Y2 - 2 February 2019 through 4 February 2019
ER -