Microfluidic capture of endothelial progenitor cells in human blood samples

• Published in: Microelectronic engineering 2013-11, Vol.111, p.262-266
• Main Authors: Li, J.J., Broqueres-You, D., Han, Z.T., He, W.T., Li, S.S., Jiang, L.M., Levy, B.I., Shi, J., Chen, Y.
• Format: Article
• Language: English
• Subjects: Blood; Buffer solutions; Channels; Circulating; Devices; Endothelial progenitor cells; Human; Microdevices; Microfluidics; Rare cell trapping; Umbilical cords
• ISSN: 0167-9317; 1873-5568
• DOI: 10.1016/j.mee.2012.11.008

Schematic of a microfluidic device for high efficient rare cell trapping. [Display omitted] ► A microfluidic device was designed for high efficiency capture of endothelial progenitor cells. ► The device was fabricated by conventional photolithography and soft lithography techniques. ► The concept was proved both numerically and experimentally using EPCs spiked in solution or blood. ► The capture rate of EPCs could be more than 50% for a cell traveling length of only 1cm. We present a method to efficiently trap circulating endothelial progenitor cells (EPCs) in human blood samples by using a microfluidic device with a short cell traveling length. This device consists of a wide channel separated into three parallel parts by two linear arrays of micro-columns. Flow-derivation microstructures are patterned on both up- and down-side walls of the center part of the channel, forcing the cells to encounter the narrowly spaced micro-columns and then be trapped with the help of specified immunological interaction. Both theoretical and experimental data confirmed the reliability of this concept. By using human umbilical cord blood-derived EPCs spiked into a buffer solution or a blood sample, we demonstrate a capture rate of more than 50% for a traveling length of only 1cm, which is clearly advantageous in terms of cell trapping efficiency and image processing speed.