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静态液滴阵列用于在隔离的化学微环境中培养单个活贴壁细胞。

Static droplet array for culturing single live adherent cells in an isolated chemical microenvironment.

机构信息

School of Mechanical and Manufacturing Engineering, University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Lab Chip. 2018 Jul 24;18(15):2156-2166. doi: 10.1039/c8lc00403j.

Abstract

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.

摘要

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。

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