4.7 Article

Transport of live yeast and zebrafish embryo on a droplet (digital'') microfluidic platform

Journal

LAB ON A CHIP
Volume 9, Issue 16, Pages 2398-2401

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b906257b

Keywords

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Funding

  1. Korean Government (MOEHRD) [KRF-2006-214-D00014]
  2. Institute for Cell Mimetic Space Exploration (CMISE
  3. NASA University Research, Engineering and Technology Institute (URETI) [NCC 2-1364]
  4. NSF [DGE0654431]
  5. National Institutes of Health [RR020070]
  6. NATIONAL CENTER FOR RESEARCH RESOURCES [R01RR020070] Funding Source: NIH RePORTER

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We demonstrate the first programmed transport of live yeast (Saccharomyces cerevisiae) and a zebrafish embryo (Danio rerio) within droplets in a two-plate digital microfluidic device. The yeast remained viable after transport, and the actuated droplets left no yeast behind. A zebrafish embryo transported 2 hours after fertilization developed normally and hatched. Dechorionation was demonstrated by mixing a droplet of digestive reagent droplet with a droplet containing the embryo. These results demonstrate the potential for using a droplet microfluidic device as an alternative to microwell plates for yeast and zebrafish assays.

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