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一种用于毒理学和药物研究的非人灵长类动物气溶胶沉积模型。

A nonhuman primate aerosol deposition model for toxicological and pharmaceutical studies.

作者信息

Martonen T B, Katz I M, Musante C J

机构信息

Mail Drop 74, National Health and Environmental Effects Research Laboratory, U.S. EPA, Research Triangle Park, NC 27711, USA.

出版信息

Inhal Toxicol. 2001 Apr;13(4):307-24. doi: 10.1080/08958370117552.

DOI:10.1080/08958370117552
PMID:11295864
Abstract

Nonhuman primates may be used as human surrogates in inhalation exposure studies to assess either the (1) adverse health effects of airborne particulate matter or (2) therapeutic effects of aerosolized drugs and proteins. Mathematical models describing the behavior and fate of inhaled aerosols may be used to complement such laboratory investigations. For example, the optimal conditions, in terms of ventilatory parameters (e.g., breathing frequency and tidal volume) and aerosol characteristics (e.g., geometric size and density), necessary to target drug delivery to specific sites within the respiratory tract may be estimated a priori with models. In this work a mathematical description of the rhesus monkey (Macaca mulatta) lung is presented for use with an aerosol deposition model. Deposition patterns of 0.01- to 5-microm-diameter monodisperse aerosols within lungs were calculated for 3 monkey lung models (using different descriptions of alveolated regions) and compared to human lung results obtained using a previously validated mathematical model of deposition physics. Our findings suggest that there are significant differences between deposition patterns in monkeys and humans. The nonhuman primates had greater exposures to inhaled substances, particularly on the basis of deposition per unit airway surface area. However, the different alveolar volumes in the rhesus monkey models had only minor effects on aerosol dosimetry within those lungs. By being aware of such quantitative differences, investigators can employ the respective primate models (human and nonhuman) to more effectively design and interpret the results of future inhalation exposure experiments.

摘要

在吸入暴露研究中,非人类灵长类动物可用作人类替代物,以评估(1)空气中颗粒物对健康的不良影响或(2)雾化药物和蛋白质的治疗效果。描述吸入气溶胶行为和归宿的数学模型可用于补充此类实验室研究。例如,利用模型可以预先估计将药物输送到呼吸道特定部位所需的最佳条件,这些条件涉及通气参数(如呼吸频率和潮气量)和气溶胶特性(如几何尺寸和密度)。在这项工作中,我们给出了恒河猴(猕猴)肺的数学描述,用于气溶胶沉积模型。针对3种猴肺模型(使用不同的肺泡区域描述)计算了直径为0.01至5微米的单分散气溶胶在肺内的沉积模式,并与使用先前验证的沉积物理数学模型获得的人肺结果进行了比较。我们的研究结果表明,猴与人的沉积模式存在显著差异。非人类灵长类动物吸入物质的暴露量更大,特别是以单位气道表面积的沉积量为基础。然而,恒河猴模型中不同的肺泡体积对这些肺内的气溶胶剂量测定只有轻微影响。通过了解这些定量差异,研究人员可以利用各自的灵长类模型(人类和非人类)更有效地设计和解释未来吸入暴露实验的结果。

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