TY - GEN
T1 - Floating microfluidic gradients
AU - Qasaimeh, M. A.
AU - Juncker, D.
PY - 2010
Y1 - 2010
N2 - We propose a concept for rapid generation of tunable, shear-free, mobile gradients in open space which we define as floating gradient. A microfluidic probe with 4 apertures arranged at the corners of a virtual square, two for injecting fluids and two for aspiration. The simultaneous injection from two apertures results to a head-to-head flow at the center of the MFP, and the formation of a stagnation point, while aspiration by the two other apertures results in hydrodynam-ic confinement of the injected streams, forming a quadrupole-like microfluidic field. The two injected streams are the source and sink, respectively, and a gradient is formed across the shear-free, stagnation point. We show that the gradient is formed rapidly, can be tuned by changing the aspiration flow rate, and can be moved either hydrodynamically by changing the flow ratio between the two aspiration apertures and/or two injection apertures, or can be moved by physically displacing the microfluidic probe. We expect the floating gradient concept to be useful for surface patterning and cell studies.
AB - We propose a concept for rapid generation of tunable, shear-free, mobile gradients in open space which we define as floating gradient. A microfluidic probe with 4 apertures arranged at the corners of a virtual square, two for injecting fluids and two for aspiration. The simultaneous injection from two apertures results to a head-to-head flow at the center of the MFP, and the formation of a stagnation point, while aspiration by the two other apertures results in hydrodynam-ic confinement of the injected streams, forming a quadrupole-like microfluidic field. The two injected streams are the source and sink, respectively, and a gradient is formed across the shear-free, stagnation point. We show that the gradient is formed rapidly, can be tuned by changing the aspiration flow rate, and can be moved either hydrodynamically by changing the flow ratio between the two aspiration apertures and/or two injection apertures, or can be moved by physically displacing the microfluidic probe. We expect the floating gradient concept to be useful for surface patterning and cell studies.
KW - Concentration gradients
KW - Microfluidic probe
KW - Stagnation point
UR - http://www.scopus.com/inward/record.url?scp=84884313674&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84884313674&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:84884313674
SN - 9781618390622
T3 - 14th International Conference on Miniaturized Systems for Chemistry and Life Sciences 2010, MicroTAS 2010
SP - 1844
EP - 1846
BT - 14th International Conference on Miniaturized Systems for Chemistry and Life Sciences 2010, MicroTAS 2010
T2 - 14th International Conference on Miniaturized Systems for Chemistry and Life Sciences 2010, MicroTAS 2010
Y2 - 3 October 2010 through 7 October 2010
ER -