Single-layer planar on-chip flow cytometer using microfluidic drifting based three-dimensional (3D) hydrodynamic focusing
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作者:
Mao, Xiaole
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Penn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Penn State Univ, Dept Bioengn, University Pk, PA 16802 USAPenn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Mao, Xiaole
[1
,2
]
Lin, Sz-Chin Steven
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Penn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USAPenn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Lin, Sz-Chin Steven
[1
]
Dong, Cheng
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Penn State Univ, Dept Bioengn, University Pk, PA 16802 USAPenn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Dong, Cheng
[2
]
Huang, Tony Jun
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Penn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Penn State Univ, Dept Bioengn, University Pk, PA 16802 USAPenn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
Huang, Tony Jun
[1
,2
]
机构:
[1] Penn State Univ, Dept Engn Sci & Mech, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Bioengn, University Pk, PA 16802 USA
In this work, we demonstrate an on-chip microfluidic flow cytometry system based on a three-dimensional (3D) hydrodynamic focusing technique, microfluidic drifting. By inducing Dean flow in a curved microfluidic channel, microfluidic drifting can be used to hydrodynamically focus cells or particles in the vertical direction and enables the 3D hydrodynamic focusing in a single-layer planar microfluidic device. Through theoretical calculation, numerical simulation, and experimental characterization, we found that the microfluidic drifting technique can be effectively applied to three-dimensionally focus microparticles with density and size equivalent to those of human CD4+ T lymphocytes. In addition, we developed a flow cytometry platform by integrating the 3D focusing device with a laser-induced fluorescence (LIF) detection system. The system was shown to provide effective high-throughput flow cytometry measurements at a rate of greater than 1700 cells s(-1).