Inertial Focusing in Triangular Microchannels for Flow Cytometry
Ian Papautsky, Professor of Bioengineering, Co-Director, NSF Center for Advanced Design & Manufacturing of Integrated Microfluidics, University of Illinois at Chicago
In the past two decades, microfluidics has become of great value in
precisely aligning cells or microparticles within fluids. Microfluidic
techniques use either external forces or sheath flow to focus
particulate samples, and face the challenges of complex instrumentation
design and limited throughput. The burgeoning field of inertial
microfluidics brings single-position focusing functionality at
throughput orders of magnitude higher than previously available.
However, most inertial microfluidic focusers rely on cross-sectional
flow-induced drag force to achieve single-position focusing, which
inevitably complicates the device design and operation. This work
presents a microfluidic device that takes advantage of asymmetric
velocity profile in a low aspect ratio triangular microchannel to focus
cells and microbeads into a single position with high efficiency, and
without the need for secondary flow, sheath flow or external forces.
The device was further integrated with a laser counting system to form a
sheathless flow cytometer, and demonstrated to count at ~1,000/s
throughput and <10% variability. Cells can be completely recovered
and remain viable. This approach offers a number of benefits, including
simplicity in fundamental principle and geometry, convenience in
design, modification and integration, flexibility in focusing of
different samples, high compatibility with real-world cellular samples
as well as high-precision and high-throughput single-position focusing.
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