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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6733285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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