Comparative Numerical Modeling of Inhaled Nanoparticle Deposition in Human and Rat Nasal Cavities

被引:31
|
作者
Dong, Jingliang [1 ]
Shang, Yidan [1 ]
Inthavong, Kiao [1 ]
Tu, Jiyuan [1 ]
Chen, Rui [2 ]
Bai, Ru [2 ]
Wang, Dongliang [2 ]
Chen, Chunying [2 ]
机构
[1] RMIT Univ, Sch Engn, POB 71, Bundoora, Vic 3083, Australia
[2] Natl Ctr Nanosci & Technol China, Beijing Key Lab Ambient Particles Hlth Effects &, CAS Ctr Excellence Nanosci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100090, Peoples R China
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
nanoparticle deposition; nasal cavity; CFD; deposition intensity; rat-human extrapolation; PARTICLE DEPOSITION; ULTRAFINE PARTICLES; AIR-FLOW; TIO2; NANOPARTICLES; LESION DISTRIBUTION; RESPIRATORY-TRACT; IN-VITRO; BRAIN; DOSIMETRY; TOXICITY;
D O I
10.1093/toxsci/kfw087
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
To gain a better understanding of nanoparticle exposure in human nasal cavities, laboratory animals (e.g. rat) are used for in vivo studies. However, due to anatomical differences between human and rodent nasal cavities, direct particle deposition comparisons between species are difficult. This paper presents a comparative nanoparticle (1 nm, 10 nm, and 100 nm) deposition study using anatomically realistic models of a human and rat nasal cavity. The particle deposition fraction was highest consistently in the main nasal passage, for all nanoparticles tested, in the human model; whereas this was only the case for 10 nm, and 100 nm particles for the rodent model, where greater deposition was found in the anterior nose for 1 nm particles. A deposition intensity (DI) term was introduced to represent the accumulated deposition fraction on cross-sectional slices. A common and preferential deposition site in the human model was found for all nanoparticles occurring at a distance of 3.5 cm inside the nasal passage. For the rodent model maximum DI occurred in the vestibule region at a distance of 0.3 cm, indicating that the rodent vestibule produces exceptionally high particle filtration capability. We also introduced a deposition flux which was a ratio of the regional deposition fraction relative to the region's surface area fraction. This value allowed direct comparison of deposition flux between species, and a regional extrapolation scaling factor was found (e.g. 1/10 scale for vestibule region for rat to human comparison). This study bridges the in vitro exposure experiments and in vivo nanomaterials toxicity studies, and can contribute towards improving inter-species exposure extrapolation studies in the future.
引用
收藏
页码:284 / 296
页数:13
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