68th Annual Meeting of the APS Division of Fluid Dynamics
Volume 60, Number 21
Sunday–Tuesday, November 22–24, 2015;
Boston, Massachusetts
Session R9: Microscale Flows: Microfluidic Devices II
12:50 PM–3:26 PM,
Tuesday, November 24, 2015
Room: 109
Chair: Matthew Hancock, Veryst Engineering
Abstract ID: BAPS.2015.DFD.R9.8
Abstract: R9.00008 : 3D flow focusing for microfluidic flow cytometry with ultrasonics
2:21 PM–2:34 PM
Authors:
Vaskar Gnyawali
(Department of Mechanical and Industrial Engineering, Ryerson University, Toronto, Canada)
Eric M. Strohm
(Department of Physics, Ryerson University, Toronto, Canada)
Yasaman Daghighi
(Department of Physics, Ryerson University, Toronto, Canada)
Mia Van de Vondervoort
(Department of Physics, Ryerson University, Toronto, Canada)
Michael C. Kolios
(Department of Physics, Ryerson University, Toronto, Canada)
Scott S.H. Tsai
(Department of Mechanical and Industrial Engineering, Ryerson University, Toronto, Canada)
We are developing a flow cytometer that detects unique acoustic signature
waves generated from single cells due to interactions between the cells and
ultrasound waves. The generated acoustic waves depend on the size and
biomechanical properties of the cells and are sufficient for identifying
cells in the medium. A microfluidic system capable of focusing cells through a
10 x 10 $\mu$m ultrasound beam cross section was developed to facilitate
acoustic measurements of single cells. The cells are streamlined in a
hydro-dynamically 3D focused flow in a 300 x 300 $\mu$m channel made
using PDMS. 3D focusing is realized by lateral sheath flows
and an inlet needle (inner diameter 100
$\mu$m). The accuracy of the 3D flow focusing is measured using a dye and
detecting its localization using confocal microscopy. Each flowing cell
would be probed by an ultrasound pulse, which has a center frequency of 375
MHz and bandwidth of 250 MHz. The same probe would also be used for
recording the scattered waves from the cells, which would be processed to
distinguish the physical and biomechanical characteristics of the cells,
eventually identifying them. This technique has potential applications in
detecting circulating tumor cells, blood cells and blood-related diseases.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2015.DFD.R9.8