Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease

In patients with fibrotic pulmonary disease such as idiopathic pulmonary fibrosis (IPF), inhaled aerosols deposit mostly in the less affected region of the lungs, resulting in suboptimal pharmacokinetics of airway-delivered treatments. Refinement of aerosol delivery technique requires new models to...

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Bibliographic Details
Published in:Frontiers in bioengineering and biotechnology Vol. 8; p. 1022
Main Authors: Le Guellec, Sandrine, Allimonnier, Laurine, Heuzé-Vourc'h, Nathalie, Cabrera, Maria, Ossant, Frédéric, Pourchez, Jérémie, Vecellio, Laurent, Plantier, Laurent
Format: Journal Article
Language:English
Published: Switzerland Frontiers 28-08-2020
Frontiers Media S.A
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Summary:In patients with fibrotic pulmonary disease such as idiopathic pulmonary fibrosis (IPF), inhaled aerosols deposit mostly in the less affected region of the lungs, resulting in suboptimal pharmacokinetics of airway-delivered treatments. Refinement of aerosol delivery technique requires new models to simulate the major alterations of lung physiology associated with IPF, i.e., heterogeneously reduced lung compliance and increased airway caliber. A novel physical model of the respiratory system was constructed to simulate aerosol drug delivery in spontaneously breathing (negative pressure ventilation) IPF patients. The model comprises upper (Alberta ideal throat) and lower airway (plastic tubing) models and branches into two compartments (Michigan lung models) which differ in compliance and caliber of conducting airway. The model was able to reproduce the heterogeneous, compliance-dependent reduction in ventilation and aerosol penetration (using NaF as a model aerosol) seen in fibrotic lung regions in IPF. Of note, intrapulmonary percussive ventilation induced a 2-3-fold increase in aerosol penetration in the low-compliance/high airway caliber compartment of the model, demonstrating the responsiveness of the model to therapeutic intervention.
Bibliography:This article was submitted to Biomaterials, a section of the journal Frontiers in Bioengineering and Biotechnology
Reviewed by: Ira Katz, Air Liquide, France; James B. Fink, Texas State University System, United States
Edited by: Josue Sznitman, Technion – Israel Institute of Technology, Israel
ISSN:2296-4185
2296-4185
DOI:10.3389/fbioe.2020.01022