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Rapid Viscoelastic Characterization of Airway Mucus Using a Benchtop Rheometer
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Mucus structure and properties in cystic fibrosis

Bruce K Rubin1

  • 1Pediatrics and Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1081, USA. brubin@wfubmc.edu <brubin@wfubmc.edu>

Paediatric Respiratory Reviews
|April 11, 2007
PubMed
Summary

Airway mucus properties are key for lung health. In cystic fibrosis (CF), altered secretions, rich in DNA and F-actin instead of mucins, impair airway clearance.

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