Colby Sean M, Kabilan Senthil, Jacob Richard E, Kuprat Andrew P, Einstein Daniel R, Corley Richard A
Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Inhal Toxicol. 2016;28(4):192-202. doi: 10.3109/08958378.2016.1150367.
Computational fluid dynamics (CFD) simulations of airflows coupled with physiologically based pharmacokinetic (PBPK) modeling of respiratory tissue doses of airborne materials have traditionally used either steady-state inhalation or a sinusoidal approximation of the breathing cycle for airflow simulations despite their differences from normal breathing patterns.
Evaluate the impact of realistic breathing patterns, including sniffing, on predicted nasal tissue concentrations of a reactive vapor that targets the nose in rats as a case study.
Whole-body plethysmography measurements from a free-breathing rat were used to produce profiles of normal breathing, sniffing and combinations of both as flow inputs to CFD/PBPK simulations of acetaldehyde exposure.
For the normal measured ventilation profile, modest reductions in time- and tissue depth-dependent areas under the curve (AUC) acetaldehyde concentrations were predicted in the wet squamous, respiratory and transitional epithelium along the main airflow path, while corresponding increases were predicted in the olfactory epithelium, especially the most distal regions of the ethmoid turbinates, versus the idealized profile. The higher amplitude/frequency sniffing profile produced greater AUC increases over the idealized profile in the olfactory epithelium, especially in the posterior region.
The differences in tissue AUCs at known lesion-forming regions for acetaldehyde between normal and idealized profiles were minimal, suggesting that sinusoidal profiles may be used for this chemical and exposure concentration. However, depending upon the chemical, exposure system and concentration and the time spent sniffing, the use of realistic breathing profiles, including sniffing, could become an important modulator for local tissue dose predictions.
传统上,气流的计算流体动力学(CFD)模拟与空气传播物质的呼吸组织剂量的基于生理的药代动力学(PBPK)建模相结合时,尽管与正常呼吸模式存在差异,但在气流模拟中要么使用稳态吸入,要么使用呼吸周期的正弦近似。
以大鼠为案例研究,评估包括嗅吸在内的实际呼吸模式对靶向鼻子的反应性蒸气预测鼻腔组织浓度的影响。
使用自由呼吸大鼠的全身体积描记法测量结果,生成正常呼吸、嗅吸以及两者组合的曲线,作为CFD/PBPK模拟乙醛暴露的流量输入。
对于正常测量的通气曲线,沿主要气流路径的湿鳞状上皮、呼吸上皮和过渡上皮中,预测乙醛浓度的曲线下面积(AUC)在时间和组织深度方面有适度降低,而与理想化曲线相比,嗅上皮尤其是筛鼻甲最远端区域的相应AUC则预测会增加。与理想化曲线相比,较高幅度/频率的嗅吸曲线在嗅上皮尤其是后部区域产生了更大的AUC增加。
正常曲线和理想化曲线之间,已知乙醛形成损伤区域的组织AUC差异很小,这表明正弦曲线可用于这种化学物质和暴露浓度。然而,根据化学物质、暴露系统和浓度以及嗅吸时间的不同,包括嗅吸在内的实际呼吸曲线的使用可能成为局部组织剂量预测的重要调节因素。