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Inhalation Toxicology
International Forum for Respiratory Research
Volume 26, 2014 - Issue 14
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Research Article

Computational modeling of nanoscale and microscale particle deposition, retention and dosimetry in the mouse respiratory tract

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Pages 829-842 | Received 17 Jan 2014, Accepted 07 Jun 2014, Published online: 06 Nov 2014
 

Abstract

Comparing effects of inhaled particles across rodent test systems and between rodent test systems and humans is a key obstacle to the interpretation of common toxicological test systems for human risk assessment. These comparisons, correlation with effects and prediction of effects, are best conducted using measures of tissue dose in the respiratory tract. Differences in lung geometry, physiology and the characteristics of ventilation can give rise to differences in the regional deposition of particles in the lung in these species. Differences in regional lung tissue doses cannot currently be measured experimentally. Regional lung tissue dosimetry can however be predicted using models developed for rats, monkeys, and humans. A computational model of particle respiratory tract deposition and clearance was developed for BALB/c and B6C3F1 mice, creating a cross-species suite of available models for particle dosimetry in the lung. Airflow and particle transport equations were solved throughout the respiratory tract of these mice strains to obtain temporal and spatial concentration of inhaled particles from which deposition fractions were determined. Particle inhalability (Inhalable fraction, IF) and upper respiratory tract (URT) deposition were directly related to particle diffusive and inertial properties. Measurements of the retained mass at several post-exposure times following exposure to iron oxide nanoparticles, micro- and nanoscale C60 fullerene, and nanoscale silver particles were used to calibrate and verify model predictions of total lung dose. Interstrain (mice) and interspecies (mouse, rat and human) differences in particle inhalability, fractional deposition and tissue dosimetry are described for ultrafine, fine and coarse particles.

Acknowledgements

The authors would like to thank Nigel Walker of the National Institute of Environmental Health Sciences and the National Toxicology Program for providing the deposition and clearance data for C60, and to the Battelle Multiscale Toxicology Initiative for providing the iron oxide particle deposition and clearance data.

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