Title of article
Droplet-Based Microfluidic Platforms for the Encapsulation and Screening of Mammalian Cells and Multicellular Organisms Original Research Article
Author/Authors
Jenifer Clausell-Tormos، نويسنده , , Diana Lieber، نويسنده , , Jean-Christophe Baret، نويسنده , , Abdeslam El-Harrak، نويسنده , , Oliver J. Miller، نويسنده , , Lucas Frenz، نويسنده , , Joshua Blouwolff، نويسنده , , Katherine J. Humphry، نويسنده , , Sarah K?ster، نويسنده , , Honey Duan، نويسنده , , Christian Holtze، نويسنده , , David A. Weitz، نويسنده , , Andrew D. Griffiths، نويسنده , , Christoph A. Merten، نويسنده ,
Issue Information
ماهنامه با شماره پیاپی سال 2008
Pages
11
From page
427
To page
437
Abstract
High-throughput, cell-based assays require small sample volumes to reduce assay costs and to allow for rapid sample manipulation. However, further miniaturization of conventional microtiter plate technology is problematic due to evaporation and capillary action. To overcome these limitations, we describe droplet-based microfluidic platforms in which cells are grown in aqueous microcompartments separated by an inert perfluorocarbon carrier oil. Synthesis of biocompatible surfactants and identification of gas-permeable storage systems allowed human cells, and even a multicellular organism (C. elegans), to survive and proliferate within the microcompartments for several days. Microcompartments containing single cells could be reinjected into a microfluidic device after incubation to measure expression of a reporter gene. This should open the way for high-throughput, cell-based screening that can use >1000-fold smaller assay volumes and has ∼500× higher throughput than conventional microtiter plate assays.
Journal title
Chemistry and Biology
Serial Year
2008
Journal title
Chemistry and Biology
Record number
1159533
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