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Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK

Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK

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The expression (equation 2.1.1) for the ur<strong>in</strong>ary excretion through 138 days was then<br />

adjusted by <strong>in</strong>clud<strong>in</strong>g data collected <strong>in</strong> the frame of the monitor<strong>in</strong>g control of occupational<br />

exposure <strong>in</strong> Los Alamos Laboratory. Three subjects were considered. They accumulated<br />

significant amounts of <strong>Plutonium</strong> dur<strong>in</strong>g wartime operations and <strong>Plutonium</strong> measurements <strong>in</strong><br />

ur<strong>in</strong>e were available up to about five years (1750 days) after their last possible exposure. This<br />

last set of data is not analogous to the previous data from volunteers because the <strong>in</strong>dividuals<br />

received unknown amounts of <strong>Plutonium</strong> over an <strong>in</strong>def<strong>in</strong>ite time period and via likely<br />

<strong>in</strong>halation route. However Langham and co-workers made an attempt to use these data: they<br />

approximated a chronic variable <strong>in</strong>take <strong>in</strong> term of an effective s<strong>in</strong>gle <strong>in</strong>take occurred at a<br />

certa<strong>in</strong> effective time between the probable limits of exposure. This was carried out us<strong>in</strong>g the<br />

aforementioned ur<strong>in</strong>ary excretion function on the short time ur<strong>in</strong>ary excretion data. Then the<br />

experimental ur<strong>in</strong>ary excretion curve was fitted aga<strong>in</strong> extend<strong>in</strong>g it to 1750 days. The result<strong>in</strong>g<br />

expression for the percentage ur<strong>in</strong>ary excretion was:<br />

35<br />

equation 2.1.3<br />

Two subjects of Langham’s study, a male and a female patient (HP-3 and HP-6),<br />

survived to their illness. Therefore further data on <strong>Plutonium</strong> biok<strong>in</strong>etics at long time after<br />

<strong>in</strong>jection became available. Samples of ur<strong>in</strong>e, feces and blood were collected at about 10,000<br />

days (around 27 years) after the <strong>in</strong>jection [88, 89, 90, 91, 92,]. A review of the orig<strong>in</strong>al<br />

<strong>in</strong>jection experimental records was later carried out and additional data were found [93]. In<br />

this work it was evident that the data reported by Langham’s group were not corrected for<br />

chemical recovery losses. Start<strong>in</strong>g from this observation all the orig<strong>in</strong>al data for the ur<strong>in</strong>ary<br />

excretion rate of <strong>Plutonium</strong> from Langham’s study (Chi-3 and from HP-1 to HP12) were<br />

reviewed [94]. Through a literary research recovery correction factors of 90% for samples<br />

collected at 0-526 days post <strong>in</strong>jection and of 67.4% at 1610-1648 days were adopted. No<br />

correction factors were necessary for samples collected at later time.<br />

2.1.1.2 Further experimental <strong>in</strong>vestigations<br />

eu = 0.20t −0.74<br />

In the last decade further studies were carried out <strong>in</strong> order to <strong>in</strong>vestigate <strong>Plutonium</strong><br />

biok<strong>in</strong>etics <strong>in</strong> humans. New experiments based on <strong>in</strong>travenous <strong>in</strong>jection of <strong>Plutonium</strong> isotopes<br />

<strong>in</strong>to healthy volunteers were designed. Yet, 239 Pu, the most important isotope <strong>in</strong> the radiation<br />

protection practice from <strong>Plutonium</strong> exposure, would have delivered a prohibitive radiation<br />

dose if <strong>in</strong>jected <strong>in</strong>to healthy subjects <strong>in</strong> the amount required for such studies. Therefore the<br />

use of other <strong>Plutonium</strong> isotopes was considered. 237 Pu resulted as one of the best candidates.<br />

Studies <strong>in</strong> rats and beagles showed 237 Pu can be a suitable metabolic tracer for other<br />

<strong>Plutonium</strong> isotopes with longer half time [95, 96]. 237 Pu, with 45.3 d half life and radioactive<br />

decay ma<strong>in</strong>ly due to electron capture (>99.99 %), delivers an effective dose significantly<br />

smaller than 239 Pu, limit<strong>in</strong>g the radiotoxicological effects for the same adm<strong>in</strong>istered amounts.<br />

For <strong>in</strong>stance <strong>in</strong> case of <strong>in</strong>gestion of 237 Pu with any f 1 values the effective dose per unit of<br />

<strong>in</strong>take is from 90 up to 2500 times smaller then 239 Pu [97]. Moreover the x rays emitted dur<strong>in</strong>g<br />

its decays would allow to study the patterns of organ uptake with direct measurement<br />

techniques. Even though all these characteristics, mak<strong>in</strong>g 237 Pu a suitable tracer for biok<strong>in</strong>etics<br />

studies, were known s<strong>in</strong>ce long time, it was not previously used because of difficulties <strong>in</strong><br />

produc<strong>in</strong>g it sufficiently free of other <strong>Plutonium</strong> isotopes potentially deliver<strong>in</strong>g much larger<br />

effective doses.

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