Sterner Teresa R, Covington Tammie R, Mattie David R
Henry M. Jackson Foundation for the Advancement of Military Medicine, Wright-Patterson Air Force Base, Dayton, OH 45433, USA.
Air Force Research Laboratory, 711HPW/RHBAF, Wright-Patterson Air Force Base, Dayton, OH 45433, USA.
Toxics. 2023 Feb 17;11(2):187. doi: 10.3390/toxics11020187.
An array physiologically-based pharmacokinetic (PBPK) model represents a streamlined method to simultaneously quantify dosimetry of multiple compounds. To predict internal dosimetry of jet fuel components simultaneously, an array PBPK model was coded to simulate inhalation exposures to one or more selected compounds: toluene, ethylbenzene, xylenes, n-nonane, n-decane, and naphthalene. The model structure accounts for metabolism of compounds in the lung and liver, as well as kinetics of each compound in multiple tissues, including the cochlea and brain regions associated with auditory signaling (brainstem and temporal lobe). The model can accommodate either diffusion-limited or flow-limited kinetics (or a combination), allowing the same structure to be utilized for compounds with different characteristics. The resulting model satisfactorily simulated blood concentration and tissue dosimetry data from multiple published single chemical rat studies. The model was then utilized to predict tissue kinetics for the jet fuel hearing loss study (JTEH A, 25:1-14). The model was also used to predict rat kinetic comparisons between hypothetical exposures to JP-8 or a Virent Synthesized Aromatic Kerosene (SAK):JP-8 50:50 blend at the occupational exposure limit (200 mg/m). The array model has proven useful for comparing potential tissue burdens resulting from complex mixture exposures.
基于生理学的药代动力学(PBPK)阵列模型是一种可同时对多种化合物剂量进行量化的简化方法。为了同时预测喷气燃料成分的体内剂量,编码了一个PBPK阵列模型,以模拟对一种或多种选定化合物(甲苯、乙苯、二甲苯、正壬烷、正癸烷和萘)的吸入暴露。该模型结构考虑了化合物在肺和肝脏中的代谢,以及每种化合物在多个组织中的动力学,包括与听觉信号相关的耳蜗和脑区(脑干和颞叶)。该模型可以采用扩散限制或血流限制动力学(或两者结合),允许对具有不同特性的化合物使用相同的结构。所得模型令人满意地模拟了多项已发表的单一化学物质大鼠研究中的血药浓度和组织剂量数据。然后,该模型被用于预测喷气燃料听力损失研究(JTEH A,25:1 - 14)中的组织动力学。该模型还被用于预测大鼠在职业接触限值(200 mg/m)下假设暴露于JP - 8或Virent合成芳烃煤油(SAK)与JP - 8 50:50混合物之间的动力学比较。该阵列模型已被证明可用于比较复杂混合物暴露导致的潜在组织负荷。