Department of Physics and School of Engineering and Applied Science, Harvard University, Cambridge, USA.
Lab Chip. 2010 Mar 21;10(6):789-94. doi: 10.1039/b915522h. Epub 2010 Jan 12.
We describe a novel microfluidic cell sorter which operates in continuous flow at high sorting rates. The device is based on a surface acoustic wave cell-sorting scheme and combines many advantages of fluorescence activated cell sorting (FACS) and fluorescence activated droplet sorting (FADS) in microfluidic channels. It is fully integrated on a PDMS device, and allows fast electronic control of cell diversion. We direct cells by acoustic streaming excited by a surface acoustic wave which deflects the fluid independently of the contrast in material properties of deflected objects and the continuous phase; thus the device underlying principle works without additional enhancement of the sorting by prior labelling of the cells with responsive markers such as magnetic or polarizable beads. Single cells are sorted directly from bulk media at rates as fast as several kHz without prior encapsulation into liquid droplet compartments as in traditional FACS. We have successfully directed HaCaT cells (human keratinocytes), fibroblasts from mice and MV3 melanoma cells. The low shear forces of this sorting method ensure that cells survive after sorting.
我们描述了一种新型的微流控细胞分选器,它可以在高速率下连续流动操作。该设备基于表面声波细胞分选方案,结合了荧光激活细胞分选 (FACS) 和荧光激活液滴分选 (FADS) 在微流道中的许多优点。它完全集成在 PDMS 设备上,并允许快速电子控制细胞转向。我们通过表面声波激发的声流来引导细胞,该声流独立于被偏转物体和连续相的材料特性的对比度来偏转流体;因此,该设备的基本原理无需通过用响应性标记物(如磁性或可极化珠)预先标记细胞来增强分选即可工作。单细胞可以直接从批量介质中以高达几千赫兹的速率进行分选,而无需像传统 FACS 那样预先封装到液滴隔室中。我们已经成功地对 HaCaT 细胞(人角质形成细胞)、来自小鼠的成纤维细胞和 MV3 黑色素瘤细胞进行了分选。这种分选方法的低剪切力确保了分选后细胞的存活。