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Internal dose assessment of 210Po using biokinetic modeling and urinary excretion measurement

机译:生物动力学模型和尿排泄量评估210 Po的内部剂量

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摘要

The mysterious death of Mr. Alexander Litvinenko who was most possibly poisoned by Polonium-210 (210Po) in November 2006 in London attracted the attention of the public to the kinetics, dosimetry and the risk of this high radiotoxic isotope in the human body. In the present paper, the urinary excretion of seven persons who were possibly exposed to traces of 210Po was monitored. The values measured in the GSF Radioanalytical Laboratory are in the range of natural background concentration. To assess the effective dose received by those persons, the time-dependence of the organ equivalent dose and the effective dose after acute ingestion and inhalation of 210Po were calculated using the biokinetic model for polonium (Po) recommended by the International Commission on Radiological Protection (ICRP) and the one recently published by Leggett and Eckerman (L&E). The daily urinary excretion to effective dose conversion factors for ingestion and inhalation were evaluated based on the ICRP and L&E models for members of the public. The ingestion (inhalation) effective dose per unit intake integrated over one day is 1.7 × 10?8 (1.4 × 10?7) Sv Bq?1, 2.0 × 10?7 (9.6 × 10?7) Sv Bq?1 over 10 days, 5.2 × 10?7 (2.0 × 10?6) Sv Bq?1 over 30 days and 1.0 × 10?6 (3.0 × 10?6) Sv Bq?1 over 100 days. The daily urinary excretions after acute ingestion (inhalation) of 1 Bq of 210Po are 1.1 × 10?3 (1.0 × 10?4) on day 1, 2.0 × 10?3 (1.9 × 10?4) on day 10, 1.3 × 10?3 (1.7 × 10?4) on day 30 and 3.6 × 10?4 (8.3 × 10?5) Bq d?1 on day 100, respectively. The resulting committed effective doses range from 2.1 × 10?3 to 1.7 × 10?2 mSv by an assumption of ingestion and from 5.5 × 10?2 to 4.5 × 10?1 mSv by inhalation. For the case of Mr. Litvinenko, the mean organ absorbed dose as a function of time was calculated using both the above stated models. The red bone marrow, the kidneys and the liver were considered as the critical organs. Assuming a value of lethal absorbed dose of 5 Gy to the bone marrow, 6 Gy to the kidneys and 8 Gy to the liver, the amount of 210Po which Mr. Litvinenko might have ingested is therefore estimated to range from 27 to 1,408 MBq, i.e 0.2–8.5 μg, depending on the modality of intake and on different assumptions about blood absorption.
机译:2006年11月,亚历山大·利特维年科先生(Alexander Litvinenko)先生的神秘死亡极有可能是在伦敦被Pol 210(210 Po)毒死的,引起了公众对动力学,剂量学以及这种高放射性同位素的风险的关注。人类的身体。在本文中,监测了可能暴露于210 Po痕迹的7个人的尿排泄。在GSF放射分析实验室中测得的值在自然本底浓度范围内。为了评估这些人接受的有效剂量,使用国际推荐的po生物动力学模型计算了器官当量剂量和急性摄入和吸入210 Po后的有效剂量的时间依赖性。放射防护委员会(ICRP),以及莱格特和埃克曼(L&E)最近发布的委员会。根据公众的ICRP和L&E模型,评估了摄入和吸入有效剂量转换因子的每日尿排泄量。一天中每单位摄入量的摄入(吸入)有效剂量为1.7×10?8 (1.4×10?7 )Sv Bq?1 ,2.0×10?7 < / sup>(9.6×10?7 )Sv Bq?1 超过10天,5.2×10?7 (2.0×10?6 )Sv Bq?1 超过30天,而1.0×10?6 (3.0×10?6 )Sv Bq?1 超过100天。在第1天,急性摄入(吸入)1 Bq的210 Po后的每日尿排泄量为1.1×10?3 (1.0×10?4 ),为2.0×10?3 (1.9×10?4 )在第10天,1.3×10?3 (1.7×10?4 )在第30天和3.6×10?4 (8.3×10?5 )Bq d?1 。假设摄入后产生的有效有效剂量范围从2.1×10?3 到1.7×10?2 mSv,从5.5×10?2 到4.5×10?1 < / sup>吸入mSv。对于利特维年科先生,使用上述两个模型计算了平均器官吸收剂量随时间的变化。红色的骨髓,肾脏和肝脏被认为是关键器官。假设对骨髓的致死吸收剂量为5 Gy,对肾脏为6 Gy,对肝脏为8 Gy,那么李特维年科先生可能摄入的210 Po的量估计为27至1,408 MBq,即0.2–8.5μg,这取决于摄入方式和对血液吸收的不同假设。

著录项

  • 来源
    《Radiation and Environmental Biophysics》 |2008年第1期|101-110|共10页
  • 作者单位

    GSF-National Research Center for Environment and Health Institute of Radiation Protection 85764 Neuherberg Germany;

    GSF-National Research Center for Environment and Health Institute of Radiation Protection 85764 Neuherberg Germany;

    GSF-National Research Center for Environment and Health Institute of Radiation Protection 85764 Neuherberg Germany;

    GSF-National Research Center for Environment and Health Institute of Radiation Protection 85764 Neuherberg Germany;

    GSF-National Research Center for Environment and Health Institute of Radiation Protection 85764 Neuherberg Germany;

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