Experimental study of diffusion-based extraction from a cell suspension |
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Authors: | Clara Mata Ellen K. Longmire David H. McKenna Katie K. Glass Allison Hubel |
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Affiliation: | (1) Department of Aerospace Engineering and Mechanics, University of Minnesota, Minneapolis, MN, USA;(2) Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA;(3) Department of Mechanical Engineering, University of Minnesota, 1100 Mechanical Engineering, 111 Church St. S.E, Minneapolis, MN 55455, USA |
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Abstract: | A recently proposed application of microfluidics is the post-thaw processing of biological cells. Numerical simulations suggest that diffusion-based extraction of the cryoprotective agent dimethyl sulfoxide (DMSO) from blood cells is viable and more efficient than centrifugation, the conventional method of DMSO removal. In order to validate the theoretical model used in these simulations, a prototype was built and the flow of two parallel streams, a suspension of Jurkat cells containing DMSO and a wash stream that contained neither cells nor DMSO, was characterized experimentally. DMSO transport in a rectangular channel (depth 500 μm, width 25 mm and overall length 125 mm) was studied as a function of three dimensionless parameters: depth ratio of the streams, cell volume fraction in the cell solution, and the Peclet number (Pe) based on channel depth, average flow rate and the diffusion coefficient for DMSO in water. In our studies, values of Pe ranged from O(103) to O(104). Laminar flow was ensured by keeping the Reynolds number between O(1) and O(10). Experimental results based on visual and quantitative data demonstrate conclusively that a microfluidic device can effectively remove DMSO from liquid and cell laden streams without compromising cell recovery. Also, flow conditions in the microfluidic device appear to have no adverse effect on cell viability at the outlet. Further, the results demonstrate that we can predict the amount of DMSO removed from a given device with the theoretical model mentioned previously. |
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Keywords: | Diffusion DMSO-extraction Cell suspension Microfluidics Channel flow |
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