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Published on: November 11, 2020
Spatial aerosol deposition correlated to anatomic feature development in 6-year-old upper airway computational models
Emily L Kolewe1, Saurav Padhye1, Ian R Woodward1
1Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, USA.
Insights
Children's upper airways change around age 6, affecting how inhaled medicines are delivered. Anatomical differences impact aerosol deposition, suggesting personalized metrics are crucial for developing pediatric therapeutics.
Area of Science:
- Pediatric respiratory system development
- Computational fluid dynamics
- Aerosol science
Background:
- Childhood upper airway anatomy differs from adults, impacting airflow and drug delivery.
- Developmental changes around age 6 influence airway geometry, such as cricoid ring shape and epiglottis angle.
- These anatomical variations can alter fluid dynamics and aerosol deposition patterns in the upper airways.
Purpose of the Study:
- To quantify pediatric-like and adult-like geometric and fluid dynamic features in 6-year-old upper airway models.
- To compare aerosol deposition in CT-scan derived models versus an idealized adult model.
- To investigate the influence of anatomical development on aerosol delivery for inhaled therapeutics.
Main Methods:
- Utilized computed tomography (CT)-scan derived models of 6-year-old upper airways.
- Employed computational fluid-particle dynamics (CFPD) to simulate airflow and particle deposition.
- Compared two subject-specific models (A and B) with varying degrees of pediatric/adult features to an idealized adult model.
Main Results:
- Distinct local fluid profiles and altered aerosol deposition were observed between models with different anatomical features.
- Subject B exhibited more pediatric-like features than Subject A.
- The idealized adult model better predicted deposition characteristics for the more adult-like Subject A model.
Conclusions:
- Anatomical development significantly influences aerosol deposition in pediatric airways.
- Personalized metrics correlating anatomy and deposition are essential for pediatric inhaled therapeutics.
- Quantifying these developmental changes can inform the design of effective pediatric aerosol delivery systems.
Abstract:
The upper airways of children undergo developmental changes around age 6, yielding differences between adult and pediatric anatomies. These differences include the cricoid ring area shape, the location of narrowest constriction, and the angle of the epiglottis, all of which are expected to alter local fluid dynamic profiles and subsequent upper airway deposition and downstream aerosol delivery of inhaled therapeutics. In this work, we quantify "pediatric"-like and "adult"-like geometric and fluid dynamic features of two computed tomography (CT)-scan derived models of 6-year-old upper airways in healthy subjects and compare to an idealized model. The two CT-scan models had a mixture of "adult"- and "pediatric"-like anatomic features, with Subject B exhibiting more "pediatric"-like features than Subject A, while the idealized model exhibited entirely "adult"-like features. By computational fluid-particle dynamics, these differences in anatomical features yielded distinct local fluid profiles with altered aerosol deposition between models. Notably, the idealized model better predicted deposition characteristics of Subject A, the more "adult"-like model, including the relationship between the impaction parameter, dp2Q and the fraction of deposition across a range of flow rates and particle diameters, as well as deposition of an approximate pharmaceutical particle size distribution model. Our results with even this limited dataset suggest that there are key personalized metrics that are influenced by anatomical development, which should be considered when developing pediatric inhalable therapeutics. Quantifying anatomical development and correlating to aerosol deposition has the potential for high-throughput developmental characterization and informing desired aerosol characteristics for pediatric applications.
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