A Microfluidic Platform for the Study of Cell Deformability
ORAL
Abstract
Reduced deformability of red blood cells (RBCs) can affect the hemodynamics in the microcirculation and reduce the oxygen transport efficiency. To this end, we developed a high-fidelity computational model of RBCs in confined microchannels to inform design decisions and fabricate a microfluidic device to measure RBC deformability. We applied our computational simulation platform to determine the appropriate deformability figure(s) of merit to quantify RBC stiffness based on an experimentally measured, steady cell shape. In particular, we determined a shape parameter based on the moment of area that is sensitive to the changes in the membrane stiffness and size. We conducted experiments and developed automatic image processing codes to track the velocity and morphology of individual RBCs within microchannels. For this purpose, we fabricated PDMS microchannels with square cross-sections (7x7 $\mu $m$^{\mathrm{2}})$ and applied a small (order 10 kPa) gauge pressure at the inlet to induce cell movement (order 10~mm s$^{\mathrm{-1}})$. Our experimental setup can record 200 cells per second, and achieve image exposure times on the order of 10~$\mu $s. This microfluidic device and supporting computational tools are intended to diagnose blood cell disorders in chronic fatigue syndrome (CFS) patients relative to the healthy controls.
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Authors
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Amir Saadat
Stanford University
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Diego A. Huyke
Stanford University
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Ingrid H. Ovreeide
Stanford University
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Diego I. Oyarzun
Stanford University
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Paulina V. Escobar
Pontificia Universidad Católica de Chile
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Juan G. Santiago
Stanford University
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Eric S. G. Shaqfeh
Stanford University