Bulletin of the American Physical Society
71st Annual Meeting of the APS Division of Fluid Dynamics
Volume 63, Number 13
Sunday–Tuesday, November 18–20, 2018; Atlanta, Georgia
Session L20: Biological Fluid Dynamics: Single Cells and Bacteria
4:05 PM–6:41 PM,
Monday, November 19, 2018
Georgia World Congress Center
Room: B308
Chair: Eva Kanso, University of Southern California
Abstract ID: BAPS.2018.DFD.L20.6
Abstract: L20.00006 : ElectroDeformation-Relaxation of Cells in Suspension to Characterize Mechanical Properties
5:10 PM–5:23 PM
Presenter:
Yasir Demiryurek
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Authors:
Yasir Demiryurek
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Seyedsajad Moazzeni
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Miao Yu
(Department of Mechanical and Aerospace Engineering, Rutgers University)
David I. Shreiber
(Department of Biomedical Engineering Rutgers University)
Jeffrey D. Zahn
(Department of Biomedical Engineering Rutgers University)
Ramsey A Foty
(Department of Surgery, Rutgers Robert Wood Johnson Medical School)
Jerry W Shan
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Liping Liu
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Hao Lin
(Department of Mechanical and Aerospace Engineering, Rutgers University)
Mechanical properties of biological cells are closely linked with their physiological and pathological states. To characterize such properties, we have developed a technique based on on-chip electrodeformation-relaxation of cells in suspension. Using an indium-tin-oxide (ITO) coated glass slide, the experimental platform set up parallel electrodes along the edge which were lithographically defined by etching ITO. Cells were exposed to high frequency and amplitude electric pulses. Images of electrodeformation and the subsequent relaxation upon pulse cessation were analyzed to quantify shape evolution during the process. Two distinctive regimes were identified by data analysis. If cells were deformed for shorter than a threshold of approximately tens of milliseconds, the relaxation timescales are independent of the pulse duration, indicating invariant mechanical properties. When deformed for longer than the threshold, the relaxation time scales linearly with the pulse duration, which is typically seen in soft glassy materials. This behavior is found to be coherent across the various cell types examined, providing insights into understanding cellular response to mechanical cues.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2018.DFD.L20.6
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