MOE Laboratory for Earth Surface Process, College of Urban and Environmental Sciences, Peking University, Beijing, 100871, China.
School of Space and Environment, Beihang University, Beijing, 100191, China.
Chemosphere. 2019 May;222:541-548. doi: 10.1016/j.chemosphere.2019.01.168. Epub 2019 Jan 31.
Constant elimination half-life is usually used in first-order one-compartment pharmacokinetic models to assess human exposure to dioxin-like polychlorinated biphenyls (PCBs). However, hepatic clearance rates are usually lower for elders than for young people. In this study, levels of 12 dioxin-like PCBs were determined in blood samples collected in 2012 from 305 individuals from the general population. We estimated the historical daily intake of dioxin-like PCBs for individuals with a validated annual exponential decay function. Based on the blood levels and historical daily intake levels, and using the maximum likelihood estimation by running the first-order one-compartment pharmacokinetic model, elimination rates were optimized as exponential functions of age for PCB118, PCB157, PCB189 and PCB126; linear functions of age for PCB114, PCB123, PCB167 and PCB169; and constant functions of age for PCB105 and PCB156. With the exception of PCB105 and PCB156, half-lives generally increased with age for individuals from 24 to 50 years old: from 0.805 to 1.95 years for PCB189, 2.08-4.54 years for PCB157, 3.32-5.58 years for PCB126, 3.52-6.81 years for PCB123, 5.24-12.29 years for PCB169, 6.60-14.40 years for PCB114, 7.50-14.01 years for PCB118, and 9.97-21.97 years for PCB167. The half-lives of PCB105 (5.79 years) and PCB156 (15.1 years) were independent of age. Our research for the first time clarified the effects of age on the elimination rate of dioxin-like PCBs in individuals from the general population, thus reducing uncertainty in future health risk assessments.
恒消除半衰期通常用于一阶单室药代动力学模型来评估人类接触二恶英类多氯联苯(PCBs)的情况。然而,老年人的肝清除率通常低于年轻人。在这项研究中,我们测定了 2012 年从一般人群中抽取的 305 个人的血液样本中二恶英类 PCB 的 12 种水平。我们利用验证的年度指数衰减函数,估计了个体的历史每日摄入量。基于血液水平和历史每日摄入量,并使用运行一阶单室药代动力学模型的最大似然估计,我们将 PCB118、PCB157、PCB189 和 PCB126 的消除率优化为年龄的指数函数;将 PCB114、PCB123、PCB167 和 PCB169 的消除率优化为年龄的线性函数;将 PCB105 和 PCB156 的消除率优化为年龄的常数函数。除了 PCB105 和 PCB156 之外,24 至 50 岁个体的半衰期通常随着年龄的增长而增加:PCB189 从 0.805 年增加到 1.95 年,PCB157 从 2.08 年增加到 4.54 年,PCB126 从 3.32 年增加到 5.58 年,PCB123 从 3.52 年增加到 6.81 年,PCB169 从 5.24 年增加到 12.29 年,PCB114 从 6.60 年增加到 14.40 年,PCB118 从 7.50 年增加到 14.01 年,PCB167 从 9.97 年增加到 21.97 年。PCB105(5.79 年)和 PCB156(15.1 年)的半衰期与年龄无关。我们的研究首次阐明了年龄对一般人群中二恶英类 PCBs 消除率的影响,从而降低了未来健康风险评估的不确定性。