Ménache M G, Miller F J, Raabe O G
Center for Extrapolation Modeling, Duke University Medical Center, Durham, NC 27710, USA.
Ann Occup Hyg. 1995 Jun;39(3):317-28.
Several inhalability curves for nose breathing in humans have been developed. No studies have been designed specifically to develop inhalability functions for animals, although it has been shown that pulmonary deposition of large particles (> 4-5 microns) via inhalation is minimal in laboratory animals [Raabe et al., Inhaled Particles VI, pp. 53-63. Pergamon Press, Oxford (1988)]. The logistic function was fitted to these animal deposition data of Raabe et al. (1988) to estimate an inhalability curve for laboratory animals. The logistic function was also fitted to the human data of Breysse and Swift [Aerosol Sci. Technol. 13, 459-464 (1990)] for comparison. The results suggest that ambient concentration is a good predictor (inhalability > 95%) of inhaled concentration for humans for particles < 11 microns dae. In small laboratory animals, however, the inhalable portion of the ambient concentration is predicted to be 95% for 0.7 microns dae particles but declines to 45% for 10 microns dae particles. It is, therefore, important to consider the effects of inhalability when estimating dose delivered to the target tissue in animals. In comparing delivered doses between animals and humans, adjusting for inhalability may change not only the magnitude of the difference but also which species is predicted to receive a greater delivered dose.
已经得出了人类经鼻呼吸的几条可吸入性曲线。虽然已经表明,在实验动物中,通过吸入方式沉积在肺部的大颗粒(>4-5微米)极少[拉贝等人,《吸入颗粒VI》,第53-63页。帕加马出版社,牛津(1988年)],但尚未专门设计研究来得出动物的可吸入性函数。将逻辑函数拟合到拉贝等人(1988年)的这些动物沉积数据上,以估计实验动物的可吸入性曲线。为了进行比较,还将逻辑函数拟合到布雷斯和斯威夫特的人体数据上[《气溶胶科学与技术》13,459-464(1990年)]。结果表明,对于粒径<11微米空气动力学当量直径(dae)的颗粒,环境浓度是人类吸入浓度的良好预测指标(可吸入性>95%)。然而,在小型实验动物中,对于0.7微米dae的颗粒,环境浓度的可吸入部分预计为95%,但对于10微米dae的颗粒则降至45%。因此,在估计给予动物靶组织的剂量时,考虑可吸入性的影响很重要。在比较动物和人类的给予剂量时,对可吸入性进行调整可能不仅会改变差异的大小,还会改变预计接受更大给予剂量的物种。