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  4. Trapping of bioparticles via microvortices in a microfluidic device for bioassay applications
 
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Trapping of bioparticles via microvortices in a microfluidic device for bioassay applications

Journal
Analytical Chemistry
Journal Volume
80
Journal Issue
23
Pages
8937-8945
Date Issued
2008
Author(s)
Cheng, M.L.
Yu, S.L.
Hsin, P.L.
Chang, Y.C.
ANDREW WO  
DOI
10.1021/ac800972t
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/485876
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-57449101858&doi=10.1021%2fac800972t&partnerID=40&md5=f3d6e819929da944e59daea90ed94dd3
Abstract
This paper presents hydrodynamic trapping of bioparticles in a microfluidic device. An in-plane oscillatory microplate, driven via Lorentz law, generates two counter-rotating microvortices, trapping the bioparticles within the confines of the microvortices. The force required to trap bioparticles is quantified by tuning the background flow and the microplate's excitation voltage. Trapping and releasing of 10-microm polystyrene beads, human embryonic kidney (HEK) cells, red blood cells (RBCs), and IgG antibodies were demonstrated. Results show the microvortices rotates at 0-6 Hz corresponding to 2-9 Vpp (peak-to-peak) excitation. At a particular rate of rotation (2-7 Vpp tested), a bioparticle is trapped until the background flow exceeds a limit. This flow limit increases with the rate of rotation, which defines the trap/release force boundary over the range of operation. This boundary is 12 +/- 2.0 pN for cell-size bioparticles and 160 +/- 50 fN for antibodies. Trapping of RBCs demonstrated microvortices' ability for nonspherical cells. Cell viability was studied via HEK cells that were trapped for 30 min and shown to be viable. This hydrodynamically controlled approach to trap a wide range of bioparticles should be useful as a microfluidic device for cellular and subcellular bioassay applications.
Type
journal article

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