• 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