a Santa Fe, New Mexico.
b Radiation Protection Division, Los Alamos National Laboratory, Los Alamos, New Mexico.
Radiat Res. 2018 Jan;189(1):64-67. doi: 10.1667/RR14852.1. Epub 2017 Nov 15.
In 2008, Serandour et al. reported on their in vitro experiment involving rat plasma samples obtained after an intravenous intake of plutonium citrate. Different amounts of DTPA were added to the plasma samples and the percentage of low-molecular-weight plutonium measured. Only when the DTPA dosage was three orders of magnitude greater than the recommended 30 μmol/kg was 100% of the plutonium apparently in the form of chelate. These data were modeled assuming three competing chemical reactions with other molecules that bind with plutonium. Here, time-dependent second-order kinetics of these reactions are calculated, intended eventually to become part of a complete biokinetic model of DTPA action on actinides in laboratory animals or humans. The probability distribution of the ratio of stability constants for the reactants was calculated using Markov Chain Monte Carlo. These calculations substantiate that the inclusion of more reactions is needed in order to be in agreement with known stability constants.
2008 年,Serandour 等人报告了他们的一项体外实验,该实验涉及静脉摄入柠檬酸钚后获得的大鼠血浆样本。向血浆样本中加入不同量的 DTPA,并测量低分子量钚的百分比。只有当 DTPA 剂量比推荐的 30 μmol/kg 高出三个数量级时,钚才明显以螯合物的形式存在。这些数据是在假设与与钚结合的其他分子发生三种竞争化学反应的情况下建模的。在这里,计算了这些反应的时变二级动力学,旨在最终成为实验室动物或人体内 DTPA 对锕系元素作用的完整生物动力学模型的一部分。使用马尔可夫链蒙特卡罗法计算了反应物稳定性常数比的概率分布。这些计算证实,需要包括更多的反应,才能与已知的稳定性常数一致。