首页|基于ICRP生物动力学模型的镅急性吸入后在主要源器官中滞留份额计算

基于ICRP生物动力学模型的镅急性吸入后在主要源器官中滞留份额计算

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目的 为了避免超铀核素镅大量吸入造成对关键靶器官的伤害,并为事故后促排或其他辐射防护措施提供依据.方法 本研究依据IAEA通用安全导则No.GSG-2的内照射事故应急准备与响应通用准则、ICRP当前最新的生物动力学模型及参数,以工作人员急性吸入241 Am[粒径AMAD 5 μm(σ=2.5)]为例建立计算程序,确定关键靶器官为肺部AI区和红骨髓,并确定造成关键靶器官短期吸收剂量的主要源器官为肺部AI区、血液、小梁骨骨表.结果 计算出241Am吸入后主要源器官中滞留份额随时间的变化.结论 镅吸收入血后从血液中快速转移,不同吸收类别镅在血液中早期滞留份额变化趋势相似,S、M、F类镅在血液中滞留份额峰值出现在0.03 d左右,到约1.7 d时衰减到峰值的一半;镅吸入后在肺部AI区、小梁骨中的早期滞留份额随时间的变化趋势有所不同:S、M类镅在肺部AI区滞留份额随时间变化较小,F类镅从肺部快速被吸收入血;小梁骨中镅,S类在前7 d快速增加,M类主要在前2周逐渐增加,F类在前2d较快速度增加.
Calculation of retention fractions in main source organs following acute americium inhalation based on ICRP biokinetic models
Objective To provide a reference for avoiding the harm to critical target organs following considerable inhala-tion exposure to the transuranium element americium(Am)as well as post-accident decorporation or other radiation protec-tion measures.Methods We established calculation programs based on the generic criteria for internal radiation emer-gency preparedness and response in the IAEA Safety Guide No.GSG-2 and current new ICRP biokinetic models and para-meters,taking an inhalation of241 Am(activity mean aerodynamic diameter of 5 μm,σ=2.5)by an adult worker as an ex-ample;and determined that the critical target organs were the lung AI region,red bone marrow,and the main source organs leading to acute doses to the critical target organs were the lung AI region,blood,and trabecular bone surface.Results The retention fractions in the main source organs over time after241 Am inhalation were calculated.Conclusion After being ab-sorbed into blood,Am moves quickly to other parts,and Am of different absorption types shows similar early changes in re-tention fractions in blood:the retention fractions of Am of S,M,and F types in blood peak around 0.03 d,and then halve around 1.7 d.Inhaled Am shows different changes over time in retention fractions in the lung AI region and trabecular bone surface in the early stage:the retention fractions of S-and M-type Am in the lung AI region change little with time,while F-type Am transfers quickly from the lung to blood;In trabecular bone surface,S-type Am increases quickly in the first 7 d,M-type Am gradually increases mainly in the first 2 weeks,and F-type Am increases quickly in the first 2 d.

ICRPBiokinetic modelCritical target organMain source organAmericiumRetention

陈倩兰、骆志平、刘森林

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中国原子能科学研究院,北京 102413

ICRP 生物动力学模型 关键靶器官 主要源器官 滞留

2024

中国辐射卫生
中华预防医学会 山东省医科院放射医学研究所

中国辐射卫生

CSTPCD
影响因子:0.35
ISSN:1004-714X
年,卷(期):2024.33(1)
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