An optical counting technique with vertical hydrodynamic focusing for biological cells

被引:12
作者
Chiavaroli, Stefano [1 ]
Newport, David [1 ]
Woulfe, Bernie [2 ]
机构
[1] Univ Limerick, Stokes Inst, M&AE, Limerick, Ireland
[2] Midwestern Reg Hosp, Midwestern Canc Ctr, Limerick, Ireland
关键词
FLOW CYTOMETERS; COULTER-COUNTER; TRACKING; CHIP;
D O I
10.1063/1.3380598
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A barrier in scaling laboratory processes into automated microfluidic devices has been the transfer of laboratory 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 leukemia, are stained with a fluorescent dye and frames of moving cells are recorded using a charge coupled device (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 favorably 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. Computational fluid dynamics (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/s is achieved. (C) 2010 American Institute of Physics. [doi:10.1063/1.3380598]
引用
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页数:10
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