Hayati Hamideh, Feng Yu, Hinsdale Myron
School of Chemical Engineering, Oklahoma State University, Stillwater, OK, USA.
Department of Physiological Sciences, Oklahoma State University, Stillwater, OK, USA.
J Aerosol Sci. 2021 May;154. doi: 10.1016/j.jaerosci.2021.105761. Epub 2021 Jan 23.
To speculate on human responses from animal studies, scale-up factors (body weight, lung volume, or lung surface area ratios) are currently used to extrapolate aerosol lung deposition from animal to human. However, those existing scale-up methods between animals and humans neglected two important inter-subject variability factors: (1) the effect of anatomical differences in respiratory systems from mouth/nose to peripheral lungs between human and rat, and (2) the effect of spatial distributions and temporal evolutions of temperature and relative humidity (RH) on droplet size change dynamics between the two species. To test the above-mentioned inter-species variability effects on droplet fates in pulmonary routes and generate correlations as a precise scale-up method for lung deposition estimation, this study simulated the transport of pure-water droplets in both human and Sprague-Dawley (SD) rat respiratory systems. Employing an experimentally validated Euler-Lagrange based Computational Fluid-Particle Dynamics (CFPD) model, simulations were performed for droplets with Stk/Fr between 8.36×10 and 1.25×10. Droplets were inhaled through human and rat nostrils with resting breathing conditions. Numerical results indicate that RH becomes uniformly distributed in rat airways sooner than in human airways, which significantly influences droplet size change dynamics and the resultant trajectories in pulmonary paths. Using the Stokes-Froude dimensionless number group (i.e., Stk/Fr) as the independent variable, the regional deposition fractions and evaporation fractions in both rat and human respiratory systems collapsed into unified correlations. The correlations can be used as a new rat-to-human scale-up method, estimating the lung depositions with consideration of anatomical differences. Furthermore, the necessity to employ realistic RH and temperature boundary conditions at airway walls was also confirmed for the accurate prediction of droplet size change using CFPD. Employing idealized boundary conditions leads the droplets to evaporate slower and deposit more than using realistic RH and temperature boundary conditions.
为了从动物研究推测人类反应,目前使用放大因子(体重、肺容积或肺表面积比)将气溶胶在肺部的沉积情况从动物外推至人类。然而,现有的动物与人类之间的放大方法忽略了两个重要的个体间变异性因素:(1)人类和大鼠从口鼻到外周肺的呼吸系统解剖差异的影响,以及(2)温度和相对湿度(RH)的空间分布和时间演变对两种物种间液滴尺寸变化动态的影响。为了测试上述种间变异性对肺部途径中液滴命运的影响,并生成相关性作为精确的放大方法用于肺沉积估计,本研究模拟了纯水液滴在人类和斯普拉格 - 道利(SD)大鼠呼吸系统中的传输。采用经过实验验证的基于欧拉 - 拉格朗日的计算流体 - 颗粒动力学(CFPD)模型,对斯托克斯数与弗劳德数之比(Stk/Fr)在8.36×10至1.25×10之间的液滴进行了模拟。液滴在静息呼吸条件下通过人类和大鼠的鼻孔吸入。数值结果表明,相对湿度在大鼠气道中比在人类气道中更快地均匀分布,这显著影响液滴尺寸变化动态以及在肺部路径中的最终轨迹。以斯托克斯 - 弗劳德无量纲数组(即Stk/Fr)作为自变量,大鼠和人类呼吸系统中的区域沉积分数和蒸发分数都汇聚成统一的相关性。这些相关性可作为一种新的从大鼠到人类的放大方法,在考虑解剖差异的情况下估计肺沉积。此外,还证实了在气道壁处采用实际的相对湿度和温度边界条件对于使用CFPD准确预测液滴尺寸变化的必要性。采用理想化边界条件会使液滴蒸发得比使用实际的相对湿度和温度边界条件时更慢且沉积更多。