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Modular microfluidic system as a model of cystic fibrosis airways

  • M. Skolimowski
  • , M. Weiss Nielsen
  • , F. Abeille
  • , P. Skafte-Pedersen
  • , D. Sabourin
  • , A. Fercher
  • , D. Papkovsky
  • , S. Molin
  • , R. Taboryski
  • , C. Sternberg
  • , M. Dufva
  • , O. Geschke
  • , J. Emnéus
  • Technical University of Denmark
  • Agilent Technologies

Research output: Contribution to journalArticlepeer-review

Abstract

A modular microfluidic airways model system that can simulate the changes in oxygen tension in different compartments of the cystic fibrosis (CF) airways was designed, developed, and tested. The fully reconfigurable system composed of modules with different functionalities: multichannel peristaltic pumps, bubble traps, gas exchange chip, and cell culture chambers. We have successfully applied this system for studying the antibiotic therapy of Pseudomonas aeruginosa, the bacteria mainly responsible for morbidity and mortality in cystic fibrosis, in different oxygen environments. Furthermore, we have mimicked the bacterial reinoculation of the aerobic compartments (lower respiratory tract) from the anaerobic compartments (cystic fibrosis sinuses) following an antibiotic treatment. This effect is hypothesised as the one on the main reasons for recurrent lung infections in cystic fibrosis patients.

Original languageEnglish
Article number034109
JournalBiomicrofluidics
Volume6
Issue number3
DOIs
Publication statusPublished - 18 Jul 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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