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CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis

BACKGROUND AND OBJECTIVE: Pulmonary fibrosis (PF) is a chronic progressive disease with an extremely high mortality rate and is a complication of COVID-19. Inhalable microspheres have been increasingly used in the treatment of lung diseases such as PF in recent years. Compared to the direct inhalati...

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Autores principales: Qin, Zhilong, Shi, Yanbin, Qiao, Jinwei, Lin, Guimei, Tang, Bingtao, Li, Xuelin, Zhang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436827/
https://www.ncbi.nlm.nih.gov/pubmed/36087437
http://dx.doi.org/10.1016/j.cmpb.2022.107094
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author Qin, Zhilong
Shi, Yanbin
Qiao, Jinwei
Lin, Guimei
Tang, Bingtao
Li, Xuelin
Zhang, Jing
author_facet Qin, Zhilong
Shi, Yanbin
Qiao, Jinwei
Lin, Guimei
Tang, Bingtao
Li, Xuelin
Zhang, Jing
author_sort Qin, Zhilong
collection PubMed
description BACKGROUND AND OBJECTIVE: Pulmonary fibrosis (PF) is a chronic progressive disease with an extremely high mortality rate and is a complication of COVID-19. Inhalable microspheres have been increasingly used in the treatment of lung diseases such as PF in recent years. Compared to the direct inhalation of drugs, a larger particle size is required to ensure the sustained release of microspheres. However, the clinical symptoms of PF may lead to the easier deposition of microspheres in the upper respiratory tract. Therefore, it is necessary to understand the effects of PF on the deposition of microspheres in the respiratory tract. METHODS: In this study, airway models with different degrees of PF in humans and mice were established, and the transport and deposition of microspheres in the airway were simulated using computational fluid dynamics. RESULTS: The simulation results showed that PF increases microsphere deposition in the upper respiratory tract and decreases bronchial deposition in both humans and mice. Porous microspheres with low density can ensure deposition in the lower respiratory tract and larger particle size. In healthy and PF humans, porous microspheres of 10 µm with densities of 700 and 400 kg/m³ were deposited most in the bronchi. Unlike in humans, microspheres larger than 4 µm are completely deposited in the upper respiratory tract of mice owing to their high inhalation velocity. For healthy and PF mice, microspheres of 6 µm with densities of and 100 kg/m³ are recommended. CONCLUSIONS: The results showed that with the exacerbation of PF, it is more difficult for microsphere particles to deposit in the subsequent airway. In addition, there were significant differences in the deposition patterns among the different species. Therefore, it is necessary to process specific microspheres from different individuals. Our study can guide the processing of microspheres and achieve differentiated drug delivery in different subjects to maximize therapeutic effects.
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spelling pubmed-94368272022-09-02 CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis Qin, Zhilong Shi, Yanbin Qiao, Jinwei Lin, Guimei Tang, Bingtao Li, Xuelin Zhang, Jing Comput Methods Programs Biomed Article BACKGROUND AND OBJECTIVE: Pulmonary fibrosis (PF) is a chronic progressive disease with an extremely high mortality rate and is a complication of COVID-19. Inhalable microspheres have been increasingly used in the treatment of lung diseases such as PF in recent years. Compared to the direct inhalation of drugs, a larger particle size is required to ensure the sustained release of microspheres. However, the clinical symptoms of PF may lead to the easier deposition of microspheres in the upper respiratory tract. Therefore, it is necessary to understand the effects of PF on the deposition of microspheres in the respiratory tract. METHODS: In this study, airway models with different degrees of PF in humans and mice were established, and the transport and deposition of microspheres in the airway were simulated using computational fluid dynamics. RESULTS: The simulation results showed that PF increases microsphere deposition in the upper respiratory tract and decreases bronchial deposition in both humans and mice. Porous microspheres with low density can ensure deposition in the lower respiratory tract and larger particle size. In healthy and PF humans, porous microspheres of 10 µm with densities of 700 and 400 kg/m³ were deposited most in the bronchi. Unlike in humans, microspheres larger than 4 µm are completely deposited in the upper respiratory tract of mice owing to their high inhalation velocity. For healthy and PF mice, microspheres of 6 µm with densities of and 100 kg/m³ are recommended. CONCLUSIONS: The results showed that with the exacerbation of PF, it is more difficult for microsphere particles to deposit in the subsequent airway. In addition, there were significant differences in the deposition patterns among the different species. Therefore, it is necessary to process specific microspheres from different individuals. Our study can guide the processing of microspheres and achieve differentiated drug delivery in different subjects to maximize therapeutic effects. Elsevier B.V. 2022-10 2022-09-02 /pmc/articles/PMC9436827/ /pubmed/36087437 http://dx.doi.org/10.1016/j.cmpb.2022.107094 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Qin, Zhilong
Shi, Yanbin
Qiao, Jinwei
Lin, Guimei
Tang, Bingtao
Li, Xuelin
Zhang, Jing
CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title_full CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title_fullStr CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title_full_unstemmed CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title_short CFD simulation of porous microsphere particles in the airways of pulmonary fibrosis
title_sort cfd simulation of porous microsphere particles in the airways of pulmonary fibrosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436827/
https://www.ncbi.nlm.nih.gov/pubmed/36087437
http://dx.doi.org/10.1016/j.cmpb.2022.107094
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