实验动物和人的上呼吸道表面积和体积:剂量学模型的考虑。

M G Ménache, L M Hanna, E A Gross, S R Lou, S J Zinreich, D A Leopold, A M Jarabek, F J Miller
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引用次数: 70

摘要

为了促进实验动物与人类区域呼吸道剂量学比较的发展,本文对已发表的上呼吸道表面积(SA)和体积(VOL)数据进行了综述。文献综述发现:(1)不同的研究采用不同的技术制备标本和测量,(2)不同的上呼吸道面积测量,(3)上呼吸道表面积和体积在一个物种内的个体数量有限,但在相对广泛的物种范围内。已发表的数据汇总在本文的表格中。在F344大鼠和女性人类受试者中进行的新测量也被提出。尽管实验方案存在差异,但可以将异速缩放方程拟合到数据中:in (SA, cm2) = -0.34 + 0.52 in(体重,g)和in (VOL, cm3) = 1.70 + 0.78 in(体重,g)。还单独拟合了大鼠的缩放方程。为了说明这些比例方程在定量人类健康风险评估中的应用,计算了丙烯醛和环氧氯丙烷在实验动物和人类中预测上呼吸道吸收的两个剂量指标(上呼吸道SA的分数吸收/cm2和分数吸收/g体重)。用动物与人的比例表示,上呼吸道SA的95%置信区间可以将预测的剂量比改变2倍。需要进一步的研究来定量地描述整个上颌上颚(从颈部到喉部),减少比例方程预测的可变性,并开发其他物种特异性的比例方程。三维成像技术提供了一种非侵入性的方法来获得人类和大型实验动物的上呼吸道表面积和体积。作为本研究的一部分,磁共振成像(MRI)和计算机断层扫描(CT)扫描的比较表明,CT图像中粘膜-空气界面的清晰度越高,为解剖特征的研究提供了更好的分辨率。然而,由于MRI成像没有与辐射暴露相关,因此在对受试者进行重复测量以阐明与正常鼻腔循环或其他生理变化相关的上呼吸道几何变化时,它比CT扫描更安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Upper respiratory tract surface areas and volumes of laboratory animals and humans: considerations for dosimetry models.

To facilitate the development of regional respiratory tract dosimetry comparisons between laboratory animal species and humans, published surface area (SA) and volume (VOL) data for the upper respiratory tract (URT) were reviewed. The review of the literature revealed that (1) different studies used different techniques to prepare specimens and make measurements, (2) different areas of the URT were measured, and (3) URT surface areas and volumes have been reported for a limited number of individual subjects within a species but for a relatively wide range of species. The published data are summarized in tables in this article. New measurements made in an F344 rat and in a female human subject are also presented. Despite the differences in experimental protocols, it was possible to fit allometric scaling equations to the data: In(SA, cm2) = -0.34 + 0.52 In(body weight, g) and In(VOL, cm3) = 1.70 + 0.78 In(body weight, g). Separate scaling equations were also fitted for rats alone. To illustrate the use of these scaling equations in quantitative human health risk assessment, two dose metrics (fractional absorption/cm2 URT SA and fractional absorption/g body weight) for predicted URT uptake in laboratory animals and humans were calculated for acrolein and epichlorohydrin. Expressed as an animal-to-human ratio, the 95% confidence interval for URT SA could change the predicted dose ratio by up to a factor of 2. Additional studies are needed to describe the entire URT (from the nares through the larynx) quantitatively and to decrease variability in scaling equation predictions as well as to develop additional species-specific scaling equations. Three-dimensional imaging techniques provide a noninvasive method to obtain URT surface areas and volumes in humans and the larger laboratory animals. Comparisons of magnetic resonance image (MRI) and computed tomography (CT) scans made as part of this study suggest that the greater clarity of the mucosal-air interface in the CT image provides better resolution for the study of anatomic features. Because there is no radiation exposure associated with MRI imaging, however, it is more safely used than CT scans in making repeated measurements in a subject to elucidate changes in URT geometry associated with normal nasal cycling or other physiological changes.

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