Andersen M E, Sarangapani R
Department of Environmental Health, CETT/Foothills Campus, Colorado State University, Ft. Collins, CO 80523, USA.
Inhal Toxicol. 2001 May;13(5):397-414. doi: 10.1080/08958370151126284.
Airstream clearance (with units of volume/time) is the volumetric flow from which chemical would have to be completely removed to account for the net loss in the nose. Extraction is the proportion of airflow from which the chemical is completely removed. Over the past several years we have developed physiologically based clearance-extraction (PBCE) models for the nose to assess the physiological, biochemical, and anatomical factors that control airstream clearance. A generic clearance equation was derived for single airway/tissue compartments that had a separate air region and either one, two, or three underlying tissue regions. For all of these structures, airstream clearance (Cl(sys)) has a common form-Equation (1)-related to tissue clearance (Cltot), gas-phase diffusional clearance (PAgas), airflow (Q), and the mucus air partition coefficient (Hmuc:a). Clsys = CltotHm:aPAgasQ/CltotHm:a(Q + PAgas) + PAgasQ. A physiologically based clearance-extraction (PBCE) model for the whole nose combined three separate nasal tissue regions, each with a four-compartment tissue stack (air, mucus, epithelial tissue, and submucosal region). A steady-state solution of the PBCE model successfully described literature results on the steady-state extraction of methyl methacrylate (MMA) and several other metabolized vapors. Model-derived tissue dosimetry estimates, that is, the amount of MMA metabolized in the target epithelial compartment of the olfactory region, for rats and humans provide dosimetric adjustment factors (DAFs) required in calculating a human reference concentration (RfC) from rodent studies. Depending on the assignment of esterase activities to sustentacular and submucosal regions, the DAFs from the PBCE model varied between 1.6 and 8.0, compared to the default value of 0.145. From the experience with MMA, a minimal data set could be defined for building the PBCE model. It consists of mucus:air and blood:air partition coefficients, metabolic constants for enzymatic hydrolysis in nasal tissues from rat and human tissues, immunohistochemistry of the distribution of these activities in rats and human olfactory tissues, and extraction studies in anesthetized rats to assess the total nasal metabolism of the test compound.
气流清除率(单位为体积/时间)是指为解释鼻腔内的净损失而必须完全清除化学物质的体积流量。提取率是指化学物质被完全清除的气流比例。在过去几年中,我们开发了基于生理学的鼻腔清除-提取(PBCE)模型,以评估控制气流清除的生理、生化和解剖学因素。针对具有单独空气区域以及一个、两个或三个下层组织区域的单个气道/组织隔室,推导了一个通用的清除方程。对于所有这些结构,气流清除率(Cl(sys))具有与组织清除率(Cltot)、气相扩散清除率(PAgas)、气流(Q)以及黏液-空气分配系数(Hmuc:a)相关的通用形式——方程(1)。Clsys = CltotHm:aPAgasQ/CltotHm:a(Q + PAgas) + PAgasQ。整个鼻腔的基于生理学的清除-提取(PBCE)模型将三个单独的鼻腔组织区域组合在一起,每个区域都有一个四隔室组织堆栈(空气、黏液、上皮组织和黏膜下层区域)。PBCE模型的稳态解成功描述了关于甲基丙烯酸甲酯(MMA)和其他几种代谢蒸气稳态提取的文献结果。模型得出的组织剂量学估计值,即嗅觉区域目标上皮隔室内代谢的MMA量,对于大鼠和人类而言,提供了在从啮齿动物研究计算人类参考浓度(RfC)时所需的剂量学调整因子(DAFs)。根据将酯酶活性分配到支持细胞和黏膜下层区域的情况,PBCE模型得出的DAFs在1.6至8.0之间,而默认值为0.145。根据对MMA的经验,可以定义一个用于构建PBCE模型的最小数据集。它包括黏液:空气和血液:空气分配系数、大鼠和人类组织中鼻腔组织酶促水解的代谢常数、这些活性在大鼠和人类嗅觉组织中分布的免疫组织化学,以及在麻醉大鼠中进行的提取研究,以评估受试化合物的全鼻代谢情况。