Journal article
Evaluating the role of sex-related structure-function differences on airway aerosol transport and deposition
Journal of applied physiology (1985), Vol.137(5), pp.1285-1300
11/01/2024
DOI: 10.1152/japplphysiol.00898.2023
PMCID: PMC11918303
PMID: 39169840
Abstract
Several experimental studies have found that females have higher deposition of particles in the airways compared with males. This has implications for the delivery of aerosolized therapeutics and for understanding sex differences in respiratory system response to environmental exposures. This study evaluates several factors that potentially contribute to sex differences in particle deposition, using scale-specific structure-function models of 1D ventilation distribution, particle transport, and deposition. The impact of gravity, inhalation flow rate, and dead space are evaluated in 12 structure-based models (seven female; five male). Females were found to have significantly higher total, bronchial, and alveolar deposition than males across a particle size range from 0.01 to 10 . Results suggest that higher deposition fraction in females is due to higher alveolar deposition for smaller particle sizes, and higher bronchial deposition for larger particles. Females had higher alveolar deposition in the lower lobes, and slightly lower particle concentration in the left upper lobe. Males were found to be more sensitive to changes due to gravity, showing greater reduction in bronchial deposition fraction. Males were also more sensitive to change in inhalation flow rate, and to scaling of dead space due to the larger male baseline airway size. Predictions of sex differences in particle deposition - that are consistent with the literature - suggest that sex-based characteristics of lung and airway size interacting with particle size gives rise to differences in regional deposition.Several experimental studies have found that females have higher deposition of particles in the airways compared with males. This has implications for the delivery of aerosolized therapeutics and for understanding sex differences in respiratory system response to environmental exposures. This study evaluates several factors that potentially contribute to sex differences in particle deposition, using scale-specific structure-function models of 1D ventilation distribution, particle transport, and deposition. The impact of gravity, inhalation flow rate, and dead space are evaluated in 12 structure-based models (seven female; five male). Females were found to have significantly higher total, bronchial, and alveolar deposition than males across a particle size range from 0.01 to 10 . Results suggest that higher deposition fraction in females is due to higher alveolar deposition for smaller particle sizes, and higher bronchial deposition for larger particles. Females had higher alveolar deposition in the lower lobes, and slightly lower particle concentration in the left upper lobe. Males were found to be more sensitive to changes due to gravity, showing greater reduction in bronchial deposition fraction. Males were also more sensitive to change in inhalation flow rate, and to scaling of dead space due to the larger male baseline airway size. Predictions of sex differences in particle deposition - that are consistent with the literature - suggest that sex-based characteristics of lung and airway size interacting with particle size gives rise to differences in regional deposition.
Details
- Title: Subtitle
- Evaluating the role of sex-related structure-function differences on airway aerosol transport and deposition
- Creators
- Ge Jin - University of AucklandHaribalan Kumar - University of AucklandAlys R ClarkKelly S Burrowes - University of AucklandEric A Hoffman - University of Iowa, RadiologyMerryn H Tawhai - University of Auckland
- Resource Type
- Journal article
- Publication Details
- Journal of applied physiology (1985), Vol.137(5), pp.1285-1300
- DOI
- 10.1152/japplphysiol.00898.2023
- PMID
- 39169840
- PMCID
- PMC11918303
- NLM abbreviation
- J Appl Physiol (1985)
- ISSN
- 1522-1601
- eISSN
- 1522-1601
- Publisher
- American Physiological Society; Rockville
- Grant note
- Dines Family TrustRoyal Society of New Zealand TeAparangi Marsden Fund: 3721976
This research was funded by a philanthropic grant (student support for G.J.) awarded to M.H.T. by the Dines Family Trust. K.S.B. was supported by a Royal Society of New Zealand TeAparangi Marsden Fund, project number 3721976
- Language
- English
- Electronic publication date
- 08/22/2024
- Date published
- 11/01/2024
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Radiology; Internal Medicine
- Record Identifier
- 9984701158602771
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