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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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Autores principales: Le Guellec, Sandrine, Allimonnier, Laurine, Heuzé-Vourc’h, Nathalie, Cabrera, Maria, Ossant, Frédéric, Pourchez, Jérémie, Vecellio, Laurent, Plantier, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483496/
https://www.ncbi.nlm.nih.gov/pubmed/32984287
http://dx.doi.org/10.3389/fbioe.2020.01022
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author Le Guellec, Sandrine
Allimonnier, Laurine
Heuzé-Vourc’h, Nathalie
Cabrera, Maria
Ossant, Frédéric
Pourchez, Jérémie
Vecellio, Laurent
Plantier, Laurent
author_facet Le Guellec, Sandrine
Allimonnier, Laurine
Heuzé-Vourc’h, Nathalie
Cabrera, Maria
Ossant, Frédéric
Pourchez, Jérémie
Vecellio, Laurent
Plantier, Laurent
author_sort Le Guellec, Sandrine
collection PubMed
description 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.
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spelling pubmed-74834962020-09-26 Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease Le Guellec, Sandrine Allimonnier, Laurine Heuzé-Vourc’h, Nathalie Cabrera, Maria Ossant, Frédéric Pourchez, Jérémie Vecellio, Laurent Plantier, Laurent Front Bioeng Biotechnol Bioengineering and Biotechnology 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. Frontiers Media S.A. 2020-08-28 /pmc/articles/PMC7483496/ /pubmed/32984287 http://dx.doi.org/10.3389/fbioe.2020.01022 Text en Copyright © 2020 Le Guellec, Allimonnier, Heuzé-Vourc’h, Cabrera, Ossant, Pourchez, Vecellio and Plantier. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Le Guellec, Sandrine
Allimonnier, Laurine
Heuzé-Vourc’h, Nathalie
Cabrera, Maria
Ossant, Frédéric
Pourchez, Jérémie
Vecellio, Laurent
Plantier, Laurent
Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title_full Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title_fullStr Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title_full_unstemmed Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title_short Low-Frequency Intrapulmonary Percussive Ventilation Increases Aerosol Penetration in a 2-Compartment Physical Model of Fibrotic Lung Disease
title_sort low-frequency intrapulmonary percussive ventilation increases aerosol penetration in a 2-compartment physical model of fibrotic lung disease
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483496/
https://www.ncbi.nlm.nih.gov/pubmed/32984287
http://dx.doi.org/10.3389/fbioe.2020.01022
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