Hydrodynamic mobility of confined polymeric particles, vesicles, and cancer cells in a square microchannel
File(s)1711.02187v2.pdf (2.44 MB)
Accepted version
Author(s)
Ahmmed, Shamim M
Suteria, Naureen S
Garbin, Valeria
Vanapalli, Siva A
Type
Journal Article
Abstract
The transport of deformable objects, including polymer particles, vesicles, and cells, has been a subject of interest for several decades where the majority of experimental and theoretical studies have been focused on circular tubes. Due to advances in microfluidics, there is a need to study the transport of individual deformable particles in rectangular microchannels where corner flows can be important. In this study, we report measurements of hydrodynamic mobility of confined polymeric particles, vesicles, and cancer cells in a linear microchannel with a square cross-section. Our operating conditions are such that the mobility is measured as a function of geometric confinement over the range 0.3 < λ < 1.5 and at specified particle Reynolds numbers that are within 0.1 < Rep < 2.5. The experimental mobility data of each of these systems is compared with the circular-tube theory of Hestroni, Haber, and Wacholder [J. Fluid Mech. 41, 689–705 (1970)] with modifications made for a square cross-section. For polymeric particles, we find that the mobility data agrees well over a large confinement range with the theory but under predicts for vesicles. The mobility of vesicles is higher in a square channel than in a circular tube, and does not depend significantly on membrane mechanical properties. The mobility of cancer cells is in good agreement with the theory up to λ ≈ 0.8, after which it deviates. Comparison of the mobility data of the three systems reveals that cancer cells have higher mobility than rigid particles but lower than vesicles, suggesting that the cell membrane frictional properties are in between a solid-like interface and a fluid bilayer. We explain further the differences in the mobility of the three systems by considering their shape deformation and surface flow on the interface. The results of this study may find potential applications in drug delivery and biomedical diagnostics.
Date Issued
2018-02-14
Date Acceptance
2018-02-02
Citation
Biomicrofluidics, 2018, 12 (1)
ISSN
1932-1058
Publisher
AIP Publishing
Journal / Book Title
Biomicrofluidics
Volume
12
Issue
1
Copyright Statement
© 2018 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in Biomicrofluidics, Vol. 12, Iss. 1, 014114 (2018) and may be found at https://dx.doi.org/10.1063/1.5018620
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000427001300018&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Physical Sciences
Biochemical Research Methods
Biophysics
Nanoscience & Nanotechnology
Physics, Fluids & Plasmas
Biochemistry & Molecular Biology
Science & Technology - Other Topics
Physics
RED-BLOOD-CELLS
LIQUID-DROPS
CREEPING MOTION
MICROPIPETTE ASPIRATION
COMPARABLE DIAMETER
NARROW CAPILLARIES
SHAPE TRANSITIONS
CYLINDRICAL TUBE
POISEUILLE FLOW
CIRCULAR TUBE
Publication Status
Published
Article Number
014114
Date Publish Online
2018-02-14