Puncher M, Harrison J D
Department of Toxicology, HPA Centre for Radiation, Chemical and Environmental Hazards, Chilton, Didcot OX11 0RQ, UK.
Radiat Prot Dosimetry. 2012 Feb;148(3):284-96. doi: 10.1093/rpd/ncr032. Epub 2011 Apr 14.
Uncertainty analyses have been performed on the biokinetic model for americium currently used by the International Commission on Radiological Protection (ICRP), and the model for plutonium recently derived by Leggett, considering acute intakes by ingestion by adult members of the public. The analyses calculated distributions of doses per unit intake. Those parameters having the greatest impact on prospective doses were identified by sensitivity analysis; the most important were the fraction absorbed from the alimentary tract, f(1), and rates of uptake from blood to bone surfaces. Probability distributions were selected based on the observed distribution of plutonium and americium in human subjects where possible; the distributions for f(1) reflected uncertainty on the average value of this parameter for non-specified plutonium and americium compounds ingested by adult members of the public. The calculated distributions of effective doses for ingested (239)Pu and (241)Am were well described by log-normal distributions, with doses varying by around a factor of 3 above and below the central values; the distributions contain the current ICRP Publication 67 dose coefficients for ingestion of (239)Pu and (241)Am by adult members of the public. Uncertainty on f(1) values had the greatest impact on doses, particularly effective dose. It is concluded that: (1) more precise data on f(1) values would have a greater effect in reducing uncertainties on doses from ingested (239)Pu and (241)Am, than reducing uncertainty on other model parameter values and (2) the results support the dose coefficients (Sv Bq(-1) intake) derived by ICRP for ingestion of (239)Pu and (241)Am by adult members of the public.
针对国际放射防护委员会(ICRP)目前使用的镅生物动力学模型以及最近由莱格特推导的钚模型,开展了不确定性分析,分析考虑了公众成年成员经口急性摄入的情况。这些分析计算了单位摄入量的剂量分布。通过敏感性分析确定了对预期剂量影响最大的那些参数;其中最重要的是从消化道吸收的分数f(1)以及从血液到骨表面的摄取率。在可能的情况下,根据在人体中观察到的钚和镅的分布情况选择概率分布;f(1)的分布反映了公众成年成员摄入未指定的钚和镅化合物时该参数平均值的不确定性。摄入(239)Pu和(241)Am后计算得到的有效剂量分布可用对数正态分布很好地描述,剂量在中心值上下变化约3倍;这些分布包含了ICRP第67号出版物中公众成年成员摄入(239)Pu和(241)Am的当前剂量系数。f(1)值的不确定性对剂量,尤其是有效剂量影响最大。得出以下结论:(1) 关于f(1)值的更精确数据在降低摄入(239)Pu和(241)Am所致剂量的不确定性方面,比降低其他模型参数值的不确定性具有更大的作用;(2) 结果支持ICRP推导的公众成年成员摄入(239)Pu和(241)Am的剂量系数(Sv Bq⁻¹摄入量)。