A barrier in scaling laboratory processes into automated microfluidic
devices has been the transfer of lab based assays: where engineering
meets biological protocol. One basic requirement is to reliably and
accurately know the distribution and number of biological cells being
dispensed. In this study, a novel optical counting technique to
efficiently quantify the number of cells flowing into a microtube is
presented. REH, B-lymphoid precursor leukaemia, are stained with a
fluorescent dye and frames of moving cells are recorded using a CCD
camera. The basic principle is to calculate the total fluorescence
intensity of the image and to divide it by the average intensity of a
single cell. This method allows counting the number of cells with an
uncertainty +/- 5%, which compares favourably to the standard
biological methodology, based on the manual Trypan Blue assay,
which is destructive to the cells and presents an uncertainty in the
order of 20%. The use of a microdevice for vertical hydrodynamic
focusing, which can reduce the background noise of out of focus cells
by concentrating the cells in a thin layer, has further improved the
technique. CFD simulation and Confocal Laser Scanning Microscopy
images have shown an 82% reduction in the vertical displacement of
the cells. For the flow rates imposed during this study, a throughput of
100-200 cells/sec is achieved.
History
Publication
Biomicrofluidics;4(2), 024110
Publisher
American Institute of Physics
Note
peer-reviewed
Other Funding information
European Commission under the Marie Curie Early Stage Training
Fellowship, Mid-Western Cancer Foundation
Rights
Copyright 2010 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, 2010, 4(2), 024110 and may be found at http://dx.doi.org/10.1063/1.3380598