School of Mechanical and Manufacturing Engineering, University of New South Wales, Sydney, NSW 2052, Australia.
Lab Chip. 2018 Jul 24;18(15):2156-2166. doi: 10.1039/c8lc00403j.
We present here a new method to easily and reliably generate an array of hundreds of dispersed nanoliter-volume semi-droplets for single-cells culture and analysis. The liquid segmentation step occurs directly in indexed traps by a tweezer-like mechanism and is stabilized by spatial confinement. Unlike common droplet-based techniques, the semi-droplet wets its surrounding trap walls thus supporting the culturing of both adherent and non-adherent cells. To eliminate cross-droplet cell migration and chemical cross-talk each semi-droplet is separated from a nearby trap by an ∼80 pL air plug. The overall setup and injection procedure takes less than 10 minutes, is insensitive to fabrication defects and supports cell recovery for downstream analysis. The method offers a new approach to easily capture, image and culture single cells in a chemically isolated microenvironment as a preliminary step towards high-throughput single-cell assays.
我们在这里提出了一种新方法,可以轻松、可靠地生成数百个分散的纳升级半液滴阵列,用于单细胞培养和分析。液滴分割步骤通过类似镊子的机制直接在索引式微阱中发生,并通过空间限制来稳定。与常见的基于液滴的技术不同,半液滴润湿其周围的微阱壁,因此可以支持贴壁和非贴壁细胞的培养。为了消除液滴间的细胞迁移和化学串扰,每个半液滴通过一个约 80 pL 的空气塞与附近的微阱隔开。整个设置和注射过程不到 10 分钟,对制造缺陷不敏感,并且支持细胞回收以进行下游分析。该方法提供了一种在化学隔离的微环境中轻松捕获、成像和培养单细胞的新方法,作为高通量单细胞分析的初步步骤。