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Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery

Pulmonary drug delivery aims to deliver particles deep into the lungs, bypassing the mouth–throat airway geometry. However, micron particles under high flow rates are susceptible to inertial impaction on anatomical sites that serve as a defense system to filter and prevent foreign particles from ent...

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Autores principales: Vara Almirall, Brenda, Inthavong, Kiao, Bradshaw, Kimberley, Singh, Narinder, Johnson, Aaron, Storey, Pippa, Salati, Hana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612176/
https://www.ncbi.nlm.nih.gov/pubmed/36297371
http://dx.doi.org/10.3390/ph15101259
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author Vara Almirall, Brenda
Inthavong, Kiao
Bradshaw, Kimberley
Singh, Narinder
Johnson, Aaron
Storey, Pippa
Salati, Hana
author_facet Vara Almirall, Brenda
Inthavong, Kiao
Bradshaw, Kimberley
Singh, Narinder
Johnson, Aaron
Storey, Pippa
Salati, Hana
author_sort Vara Almirall, Brenda
collection PubMed
description Pulmonary drug delivery aims to deliver particles deep into the lungs, bypassing the mouth–throat airway geometry. However, micron particles under high flow rates are susceptible to inertial impaction on anatomical sites that serve as a defense system to filter and prevent foreign particles from entering the lungs. The aim of this study was to understand particle aerodynamics and its possible deposition in the mouth–throat airway that inhibits pulmonary drug delivery. In this study, we present an analysis of the aerodynamics of inhaled particles inside a patient-specific mouth–throat model generated from MRI scans. Computational Fluid Dynamics with a Discrete Phase Model for tracking particles was used to characterize the airflow patterns for a constant inhalation flow rate of 30 L/min. Monodisperse particles with diameters of 7 [Formula: see text] m to 26 [Formula: see text] m were introduced to the domain within a 3 cm-diameter sphere in front of the oral cavity. The main outcomes of this study showed that the time taken for particle deposition to occur was 0.5 s; a narrow stream of particles (medially and superiorly) were transported by the flow field; larger particles > 20 [Formula: see text] m deposited onto the oropharnyx, while smaller particles < 12 [Formula: see text] m were more disperse throughout the oral cavity and navigated the curved geometry and laryngeal jet to escape through the tracheal outlet. It was concluded that at a flow rate of 30 L/min the particle diameters depositing on the larynx and trachea in this specific patient model are likely to be in the range of 7 [Formula: see text] m to 16 [Formula: see text] m. Particles larger than 16 [Formula: see text] m primarily deposited on the oropharynx.
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spelling pubmed-96121762022-10-28 Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery Vara Almirall, Brenda Inthavong, Kiao Bradshaw, Kimberley Singh, Narinder Johnson, Aaron Storey, Pippa Salati, Hana Pharmaceuticals (Basel) Article Pulmonary drug delivery aims to deliver particles deep into the lungs, bypassing the mouth–throat airway geometry. However, micron particles under high flow rates are susceptible to inertial impaction on anatomical sites that serve as a defense system to filter and prevent foreign particles from entering the lungs. The aim of this study was to understand particle aerodynamics and its possible deposition in the mouth–throat airway that inhibits pulmonary drug delivery. In this study, we present an analysis of the aerodynamics of inhaled particles inside a patient-specific mouth–throat model generated from MRI scans. Computational Fluid Dynamics with a Discrete Phase Model for tracking particles was used to characterize the airflow patterns for a constant inhalation flow rate of 30 L/min. Monodisperse particles with diameters of 7 [Formula: see text] m to 26 [Formula: see text] m were introduced to the domain within a 3 cm-diameter sphere in front of the oral cavity. The main outcomes of this study showed that the time taken for particle deposition to occur was 0.5 s; a narrow stream of particles (medially and superiorly) were transported by the flow field; larger particles > 20 [Formula: see text] m deposited onto the oropharnyx, while smaller particles < 12 [Formula: see text] m were more disperse throughout the oral cavity and navigated the curved geometry and laryngeal jet to escape through the tracheal outlet. It was concluded that at a flow rate of 30 L/min the particle diameters depositing on the larynx and trachea in this specific patient model are likely to be in the range of 7 [Formula: see text] m to 16 [Formula: see text] m. Particles larger than 16 [Formula: see text] m primarily deposited on the oropharynx. MDPI 2022-10-13 /pmc/articles/PMC9612176/ /pubmed/36297371 http://dx.doi.org/10.3390/ph15101259 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vara Almirall, Brenda
Inthavong, Kiao
Bradshaw, Kimberley
Singh, Narinder
Johnson, Aaron
Storey, Pippa
Salati, Hana
Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title_full Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title_fullStr Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title_full_unstemmed Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title_short Flow Patterns and Particle Residence Times in the Oral Cavity during Inhaled Drug Delivery
title_sort flow patterns and particle residence times in the oral cavity during inhaled drug delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612176/
https://www.ncbi.nlm.nih.gov/pubmed/36297371
http://dx.doi.org/10.3390/ph15101259
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