A quantitative framework for animal-to-human extrapolation of inhaled aerosols using species-specific respiratory dosimetry.

IF 10.9 2区 医学 Q1 TOXICOLOGY
Ji-Hun Jang, Seung-Hyun Jeong
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引用次数: 0

Abstract

Quantitative extrapolation of inhalation toxicity data from experimental animals to humans remains challenging because identical external aerosol exposures do not necessarily produce equivalent internal respiratory doses across species. This study aimed to establish a quantitative computational framework for animal-to-human extrapolation by integrating species-specific respiratory dosimetry using the Multiple-Path Particle Dosimetry (MPPD) model. Species-specific respiratory dosimetry models were developed for mice, rats, and adult humans using MPPD v3.04 under identical aerosol exposure conditions. Regional respiratory deposition was compared across species, while the effects of aerosol particle size (mass median aerodynamic diameter, MMAD) and human breathing scenarios were systematically evaluated. Regional deposition outputs were further integrated to derive quantitative dosimetry indices, human equivalent concentrations (HECs), and species correction factors (SCFs) for animal-to-human extrapolation. Marked interspecies differences were observed in regional respiratory deposition despite identical aerosol exposure conditions. Rodents exhibited predominant deposition within the extrathoracic region, whereas humans demonstrated substantially greater pulmonary deposition. Species-specific deposition differences became more pronounced with increasing MMAD, and pulmonary delivery in humans was strongly influenced by breathing scenario. Quantitative dosimetry analysis demonstrated that pulmonary deposition in humans was approximately three-fold greater than in rodents under the reference exposure condition, resulting in substantially different regional respiratory deposition metric despite equivalent external exposures. The proposed HEC and SCF metrics enabled quantitative comparison and translation of animal and human exposure conditions using MPPD-derived regional deposition metrics rather than external aerosol concentration alone. This study presents a species-specific respiratory dosimetry framework for quantitative animal-to-human extrapolation of inhaled aerosols. By integrating regional respiratory deposition with HEC and SCF analyses, the proposed framework provides a mechanistically informed strategy for inhalation dosimetry, human equivalent exposure estimation, and future integration with physiologically based pharmacokinetic modeling and inhalation risk assessment.

使用物种特异性呼吸剂量法对吸入气溶胶进行动物对人类外推的定量框架。
从实验动物到人类的吸入毒性数据的定量外推仍然具有挑战性,因为相同的外部气溶胶暴露不一定会在不同物种之间产生相同的内部呼吸剂量。本研究旨在利用多路径粒子剂量学(Multiple-Path Particle dose, MPPD)模型整合物种特异性呼吸剂量学,建立动物对人类外推的定量计算框架。在相同的气溶胶暴露条件下,使用MPPD v3.04建立了小鼠、大鼠和成年人的物种特异性呼吸剂量学模型。比较了不同物种间的区域呼吸沉积,系统评价了气溶胶粒径(空气动力质量中值直径,MMAD)和人类呼吸情景的影响。进一步整合区域沉积输出,得出定量剂量学指数、人类当量浓度(HECs)和物种校正因子(SCFs),用于动物到人类的外推。尽管相同的气溶胶暴露条件,但在区域呼吸沉积中观察到明显的种间差异。啮齿类动物主要表现为胸外区域的沉积,而人类则表现为肺沉积。随着MMAD的增加,物种特异性沉积差异变得更加明显,人类的肺输送受到呼吸情景的强烈影响。定量剂量学分析表明,在参考暴露条件下,人类的肺部沉积大约是啮齿动物的三倍,导致尽管相同的外部暴露,但区域呼吸沉积度量却存在很大差异。提出的HEC和SCF指标可以使用mppd衍生的区域沉积指标而不是单独的外部气溶胶浓度,对动物和人类的暴露条件进行定量比较和转化。本研究提出了一种物种特异性呼吸剂量学框架,用于定量动物对人类吸入气溶胶的外推。通过将区域呼吸沉积与HEC和SCF分析相结合,所提出的框架为吸入剂量学、人体等效暴露估计以及未来基于生理学的药代动力学建模和吸入风险评估提供了一种机制信息策略。
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来源期刊
Archives of Toxicology
Archives of Toxicology 医学-毒理学
CiteScore
11.60
自引率
4.90%
发文量
218
审稿时长
1.5 months
期刊介绍: Archives of Toxicology provides up-to-date information on the latest advances in toxicology. The journal places particular emphasis on studies relating to defined effects of chemicals and mechanisms of toxicity, including toxic activities at the molecular level, in humans and experimental animals. Coverage includes new insights into analysis and toxicokinetics and into forensic toxicology. Review articles of general interest to toxicologists are an additional important feature of the journal.
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