Occupational Intakes of Radionuclides Part 1 - ICRP
Occupational Intakes of Radionuclides Part 1 - ICRP
Occupational Intakes of Radionuclides Part 1 - ICRP
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
1185<br />
1186<br />
1187<br />
1188<br />
1189<br />
1190<br />
1191<br />
1192<br />
1193<br />
1194<br />
1195<br />
1196<br />
1197<br />
1198<br />
1199<br />
1200<br />
1201<br />
1202<br />
1203<br />
1204<br />
1205<br />
1206<br />
1207<br />
1208<br />
1209<br />
1210<br />
1211<br />
1212<br />
1213<br />
1214<br />
1215<br />
1216<br />
1217<br />
1218<br />
1219<br />
1220<br />
1221<br />
1222<br />
1223<br />
1224<br />
1225<br />
1226<br />
1227<br />
1228<br />
1229<br />
DRAFT REPORT FOR CONSULTATION<br />
1.6.2 Adult Reference Computational Phantoms, Publication 110 (<strong>ICRP</strong>,<br />
2009)<br />
(39) Traditionally, stylised computational phantoms <strong>of</strong> human anatomy have been<br />
utilised for assembling dose coefficients for both external and internal radiation<br />
protection. These phantoms are constructed using mathematical surface equations to<br />
describe internal organ anatomy and exterior body surfaces <strong>of</strong> reference individuals<br />
(Cristy, 1980; Cristy and Eckerman, 1987), and as such, are limited in their ability to<br />
capture true anatomic realism completely. As an alternative format for radiation<br />
transport simulation, voxel phantoms are based on segmented tomographic data <strong>of</strong><br />
real individuals obtained from computed tomography or magnetic resonance imaging<br />
(Zankl et al, 2002, 2003, 2007). As outlined above, the 2007 Recommendations<br />
adopted the use <strong>of</strong> realistic anatomical models for the revision <strong>of</strong> dose coefficients for<br />
both internal and external radiation sources. Publication 110 (<strong>ICRP</strong>, 2009) describes<br />
the development and intended use <strong>of</strong> the computational phantoms <strong>of</strong> the <strong>ICRP</strong> adult<br />
Reference Male and Reference Female. The reference phantoms were constructed<br />
after modifying the voxel models <strong>of</strong> two individuals whose body height and mass<br />
closely matched reference values. Organ volumes <strong>of</strong> both models were adjusted to<br />
yield organ masses consistent with <strong>ICRP</strong> reference data given in Publication 89<br />
(<strong>ICRP</strong>, 2002a) without compromising their anatomic realism regarding organ shape,<br />
depth, and position in the body. The report describes the methods used for this<br />
process and the anatomical and computational characteristics <strong>of</strong> the resulting<br />
phantoms.<br />
(40) The computational phantoms <strong>of</strong> adult Reference Male and Female may be<br />
used, together with codes that simulate radiation transport and energy deposition, for<br />
the assessment <strong>of</strong> the mean absorbed dose, DT, in an organ or tissue T, from which<br />
equivalent doses and the effective dose may be successively calculated.<br />
1.6.3 Advances in skeletal dosimetry<br />
(41) In this report, the skeletal dosimetry models <strong>of</strong> Publication 30 (<strong>ICRP</strong>, 1979)<br />
have been substantially updated for all radiations emitted from internalised<br />
radionuclides – alpha particles, electrons, beta particles, photons, and neutrons (e.g.<br />
from spontaneous fission). Improvements over the Publication 30 model include a<br />
more refined treatment <strong>of</strong> the dependence <strong>of</strong> the absorbed fraction on particle energy,<br />
marrow cellularity, and bone-specific spongiosa micro-architecture. Two reference<br />
sets <strong>of</strong> skeletal images were established for radiation transport simulation. The first<br />
included 1-mm ex vivo CT images <strong>of</strong> some 38 skeletal sites harvested from a 40-year<br />
male cadaver (Hough et al, 2011). These images were used to establish fractional<br />
volumes <strong>of</strong> cortical bone, trabecular spongiosa, and medullary cavities by skeletal<br />
site, and to serve as the macroscopic geometric model for particle transport. The<br />
second included 30-µm microCT images <strong>of</strong> cored samples <strong>of</strong> trabecular spongiosa to<br />
establish fractional volumes <strong>of</strong> trabecular bone and marrow tissues, and to serve as<br />
the microscopic geometric model for particle transport. Both image sets were then<br />
combined during paired-image radiation transport (PIRT) <strong>of</strong> internally emitted<br />
electrons (Shah et al, 2005). Source tissues were: bone marrow (active and inactive),<br />
35