| Literature DB >> 29922784 |
Amin Hassanzadeh-Barforoushi1, Andrew M K Law, Abbas Hejri, Mohsen Asadnia, Christopher J Ormandy, David Gallego-Ortega, Majid Ebrahimi Warkiani.
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.Entities:
Mesh:
Year: 2018 PMID: 29922784 DOI: 10.1039/c8lc00403j
Source DB: PubMed Journal: Lab Chip ISSN: 1473-0189 Impact factor: 6.799