Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK
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 structure of Polig’s skeleton model is characterized by an <strong>in</strong>itial deposition on<br />
both surface and volume bone compartments and not only on cortical surface as assumed <strong>in</strong><br />
ICRP 67 model. Furthermore a transfer of activity from volume to surface compartments<br />
(dashed arrows <strong>in</strong> Figure 3.1.9) is theoretically <strong>in</strong>troduced to achieve maximum generality <strong>in</strong><br />
skeleton modell<strong>in</strong>g by consider<strong>in</strong>g a possible local recirculation too. As presently there is no<br />
experimental evidence of such process, it was not longer considered <strong>in</strong> this skeleton model.<br />
The two models differ <strong>in</strong> the transfer rates values too, as given <strong>in</strong> Table 3.1.6.<br />
Table 3.1.6 Transfer rates of the skeletal models <strong>in</strong> ICRP 67 and Polig [157].<br />
Parameter<br />
99<br />
Value [d -1 ].<br />
ICRP 67 Polig<br />
Blood compartment to Trabecular surface 0.1941 0.226<br />
Blood compartment to Trabecular volume N.A. 0.0716<br />
Blood compartment to Cortical surface 0.1294 0.0952<br />
Blood compartment to Cortical volume N.A. 0.00448<br />
Trabecular surface to marrow 0.000493 0.00159<br />
Trabecular volume to marrow 0.000493 0.00159<br />
Trabecular surface to volume 0.000247 N.A.<br />
Cortical surface to marrow 0.0000821 0.000156<br />
Cortical volume to marrow 0.0000821 0.0000822<br />
Cortical surface to volume 0.0000411 N.A.<br />
Trabecular/Cortical marrow to blood compartment 0.0076 0.0076<br />
By compar<strong>in</strong>g the transfer rates for the two skeletal models it can be po<strong>in</strong>ted out that<br />
Polig’s model is characterized by a higher transfer of activity to the trabecular bone (+53%)<br />
and slightly smaller (-23%) to the cortical bone. The f<strong>in</strong>al effect is a generally higher activity<br />
transfer to the whole skeleton. Furthermore the skeletal transfer rates of Polig’s model are<br />
generally higher then those ones of ICRP 67 model. On the basis of such prelim<strong>in</strong>ary<br />
considerations two aspects will characterize Polig’s model <strong>in</strong> comparison to ICRP 67 one:<br />
• <strong>in</strong>itial higher deposition <strong>in</strong>to the skeleton;<br />
• a lower retention <strong>in</strong> the skeleton at long time with a higher transfer of activity to the blood<br />
compartment.<br />
These considerations are confirmed by analyz<strong>in</strong>g the biok<strong>in</strong>etics of <strong>Plutonium</strong> <strong>in</strong> a<br />
study compartmental model composed by just a transfer (blood) compartment connected to<br />
the skeletal model (Polig or ICRP67). The activity retention <strong>in</strong> skeleton and blood<br />
compartments was calculated and is presented <strong>in</strong> Figure 3.1.10 for both skeletal models. As<br />
prelim<strong>in</strong>arily argued on the basis of the transfer rates <strong>in</strong> Table 3.1.6, the <strong>in</strong>itial amount<br />
reta<strong>in</strong>ed <strong>in</strong> the skeleton is slightly higher if Polig’s model is adopted. More significantly at<br />
<strong>in</strong>termediate and long time Polig’s skeletal model predicts a lower <strong>Plutonium</strong> retention than<br />
ICRP 67 and, consequently, the blood compartment conta<strong>in</strong>s a higher amount of activity. For<br />
example at 1,000 days post <strong>in</strong>take the use of Polig’s skeletal model yields skeleton and blood