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Occupational Intakes of Radionuclides Part 1 - ICRP

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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 />

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