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Evaluating Regional Pulmonary Deposition using Patient-Specific 3D Printed Lung Models
Published on: November 11, 2020
Quantifying Olfactory and Alveolar Deposition of Ultrafine Particles Using Multiscale Modeling: Implications for
Karine Sartelet1, Lya Lugon1, Soo-Jin Park1
1CEREA, ENPC, Institut Polytechnique de Paris, EDF R&D, IPSL, 77 455 Marne la Vallée, France.
Ultrafine particles (UFPs) disproportionately impact lung and brain exposure via surface area, not mass. Children face higher deposition doses, highlighting the need for particle size-specific health risk assessments.
Area of Science:
- Environmental Health
- Atmospheric Science
- Toxicology
Background:
- Current atmospheric particle exposure metrics (e.g., PM2.5 mass) underestimate health risks by neglecting particle surface area and direct brain pathways.
- Ultrafine particles (UFPs), though low in mass, significantly contribute to deposited surface area in the lungs and olfactory region.
Purpose of the Study:
- To quantify particle deposition using lung-deposited surface area (LDSA) and olfactory deposition, considering hygroscopic growth.
- To evaluate the role of UFPs and particle size in deposition and potential brain translocation.
- To investigate disparities in particle deposition doses across populations and sources.
Main Methods:
- Multiscale atmospheric modeling (continental to street level) validated with NO2, PM mass, composition, and size-resolved particle data.
- Calculation of lung-deposited surface area (LDSA) and olfactory deposition, incorporating particle hygroscopic growth.
- Source apportionment and population-specific dose estimations.
Main Results:
- UFPs constitute over one-third of alveolar deposition in urban areas; particles <400 nm dominate lung deposition despite low PM2.5 mass contribution.
- A persistent decoupling exists between PM2.5 mass and deposited surface area across various settings and populations.
- Children experience ~3-fold higher alveolar doses than adults; residential wood heating impacts winter deposition, while traffic influences particle number and olfactory deposition.
Conclusions:
- Particle surface area, particularly from UFPs, is a critical metric for assessing respiratory and direct brain exposure, surpassing mass-based measures.
- Olfactory deposition of UFPs may be a dominant pathway for brain particle delivery, exceeding blood-borne translocation.
- Source-specific and population-specific analyses are crucial for understanding and mitigating particle-related health risks, especially for vulnerable groups like children.
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