Biomicrofluidics. 2012 Jun;6(2):24120-2412010. doi: 10.1063/1.4718719. Epub 2012 May 16.
This study presents a method for density-based separation of monodisperse encapsulated cells using a standing surface acoustic wave (SSAW) in a microchannel. Even though monodisperse polymer beads can be generated by the state-of-the-art technology in microfluidics, the quantity of encapsulated cells cannot be controlled precisely. In the present study, mono-disperse alginate beads in a laminar flow can be separated based on their density using acoustophoresis. A mixture of beads of equal sizes but dissimilar densities was hydrodynamically focused at the entrance and then actively driven toward the sidewalls by a SSAW. The lateral displacement of a bead is proportional to the density of the bead, i.e., the number of encapsulated cells in an alginate bead. Under optimized conditions, the recovery rate of a target bead group (large-cell-quantity alginate beads) reached up to 97% at a rate of 2300 beads per minute. A cell viability test also confirmed that the encapsulated cells were hardly damaged by the acoustic force. Moreover, cell-encapsulating beads that were cultured for 1 day were separated in a similar manner. In conclusion, this study demonstrated that a SSAW can successfully separate monodisperse particles by their density. With the present technique for separating cell-encapsulating beads, the current cell engineering technology can be significantly advanced.
本研究提出了一种使用微通道中的驻波表面声波(SSAW)对单分散包封细胞进行密度分离的方法。尽管通过微流控技术可以生成单分散的聚合物珠,但无法精确控制包封细胞的数量。在本研究中,可以基于声泳作用通过密度对层流中的单分散藻酸盐珠进行分离。具有相等尺寸但不同密度的珠的混合物在入口处被水动力聚焦,然后通过 SSAW 主动驱动到侧壁。珠的横向位移与珠的密度成正比,即藻酸盐珠中包封的细胞数量。在优化条件下,目标珠组(含大量细胞的藻酸盐珠)的回收率高达 97%,每分钟可回收 2300 个珠。细胞活力测试也证实,声力几乎不会对包封的细胞造成损伤。此外,培养 1 天后的细胞包封珠也以类似的方式进行了分离。总之,本研究表明 SSAW 可以成功地根据密度分离单分散颗粒。使用这种分离细胞包封珠的技术,可以显著推进当前的细胞工程技术。