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Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler

A biophysical lung model was designed to predict inhaled drug deposition in patients with obstructive airway disease, and quantitatively investigate sources of deposition variability. Different mouth-throat anatomies at varying simulated inhalation flows were used to calculate the lung dose of indac...

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Autores principales: Dolovich, Myrna B., Kuttler, Andreas, Dimke, Thomas J., Usmani, Omar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733285/
https://www.ncbi.nlm.nih.gov/pubmed/31517283
http://dx.doi.org/10.1016/j.ijpx.2019.100018
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author Dolovich, Myrna B.
Kuttler, Andreas
Dimke, Thomas J.
Usmani, Omar S.
author_facet Dolovich, Myrna B.
Kuttler, Andreas
Dimke, Thomas J.
Usmani, Omar S.
author_sort Dolovich, Myrna B.
collection PubMed
description A biophysical lung model was designed to predict inhaled drug deposition in patients with obstructive airway disease, and quantitatively investigate sources of deposition variability. Different mouth-throat anatomies at varying simulated inhalation flows were used to calculate the lung dose of indacaterol/glycopyrronium [IND/GLY] 110/50 µg (QVA149) from the dry-powder inhaler Breezhaler(®). Sources of variability in lung dose were studied using computational fluid dynamics, supported by aerosol particle sizing measurements, particle image velocimetry and computed tomography. Anatomical differences in mouth-throat geometries were identified as a major source of inter-subject variability in lung deposition. Lung dose was similar across inhalation flows of 30–120 L/min with a slight drop in calculated delivery at high inspiratory flows. Delivery was relatively unaffected by inhaler inclination angle. The delivered lung dose of the fixed-dose combination IND/GLY matched well with corresponding monotherapy doses. This biophysical model indicates low extra-thoracic drug loss and consistent lung delivery of IND/GLY, independent of inhalation flows. This is an important finding for patients across various ages and lung disease severities. The model provides a quantitative, mechanistic simulation of inhaled therapies that could provide a test system for estimating drug delivery to the lung and complement traditional clinical studies.
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spelling pubmed-67332852019-09-12 Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler Dolovich, Myrna B. Kuttler, Andreas Dimke, Thomas J. Usmani, Omar S. Int J Pharm X Article A biophysical lung model was designed to predict inhaled drug deposition in patients with obstructive airway disease, and quantitatively investigate sources of deposition variability. Different mouth-throat anatomies at varying simulated inhalation flows were used to calculate the lung dose of indacaterol/glycopyrronium [IND/GLY] 110/50 µg (QVA149) from the dry-powder inhaler Breezhaler(®). Sources of variability in lung dose were studied using computational fluid dynamics, supported by aerosol particle sizing measurements, particle image velocimetry and computed tomography. Anatomical differences in mouth-throat geometries were identified as a major source of inter-subject variability in lung deposition. Lung dose was similar across inhalation flows of 30–120 L/min with a slight drop in calculated delivery at high inspiratory flows. Delivery was relatively unaffected by inhaler inclination angle. The delivered lung dose of the fixed-dose combination IND/GLY matched well with corresponding monotherapy doses. This biophysical model indicates low extra-thoracic drug loss and consistent lung delivery of IND/GLY, independent of inhalation flows. This is an important finding for patients across various ages and lung disease severities. The model provides a quantitative, mechanistic simulation of inhaled therapies that could provide a test system for estimating drug delivery to the lung and complement traditional clinical studies. Elsevier 2019-05-30 /pmc/articles/PMC6733285/ /pubmed/31517283 http://dx.doi.org/10.1016/j.ijpx.2019.100018 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Dolovich, Myrna B.
Kuttler, Andreas
Dimke, Thomas J.
Usmani, Omar S.
Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title_full Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title_fullStr Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title_full_unstemmed Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title_short Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
title_sort biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733285/
https://www.ncbi.nlm.nih.gov/pubmed/31517283
http://dx.doi.org/10.1016/j.ijpx.2019.100018
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