Objective: To calculate depth-weighted doses for 223 Ra, 212 Pb and 225 Ac for the skin sites of trunk, arms/legs, face, wrist, back of hand, fingertip, back and side of fingers using VARSKIN+v1.2.
Methods: Published depth distribution histograms of the basal cells were used with dose averaging in VARSKIN+v1.2. A density correction factor was applied for the 1 g/cc within VARSKIN. Results were compared to the regulatory 70 µm depth and to average depth values for the skin sites.
Results: 223 Ra has no alpha component at the regulatory 70 µm. This dose is exceeded by the depth-weighted dose rates for all sites (except the fingertip) with factors ×74 (back of finger) to x3600 (trunk). 212 Pb and 225 Ac have alpha contributions at 70 µm. . For 212 Pb, this dose value is greater by over ×2 than the depth-weighted dose rate for the wrist, back of hand, and finger sites, and underestimates dose rates for the other sites. For 225 Ac, the 70µm dose rate is exceeded by the depth-weighted dose rates for the trunk, face, arms/legs by factors of ×4-10. Using fixed depth values, the depth-weighted dose rates are larger for all sites except the fingertip. The skin dose is also calculated for biological half-lives of 1, 3 and 6 h. Using the depth-weighted dose rates and a 3 h biological half-life, the activity for 500 mSv is in the range 9-177 Bq for the trunk, face, arms/legs, wrist and hand for all three radionuclides.
Conclusion: For alpha-emitting radionuclides a depth-weighted calculation gives more representative dose values. The very low activity values for 500 mSv skin dose to be exceeded have implications for appropriate staff PPE and training.
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http://dx.doi.org/10.1097/MNM.0000000000001808 | DOI Listing |
Nucl Med Commun
March 2024
Department of Physics and Nuclear Medicine, City Hospital, Sandwell and W Birmingham Hospitals NHS Trust, Birmingham, UK.
Objective: To calculate depth-weighted doses for 223 Ra, 212 Pb and 225 Ac for the skin sites of trunk, arms/legs, face, wrist, back of hand, fingertip, back and side of fingers using VARSKIN+v1.2.
Methods: Published depth distribution histograms of the basal cells were used with dose averaging in VARSKIN+v1.
Med Phys
February 2017
J Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, 32611-6131, USA.
Purpose: The hematopoietically active (or red) bone marrow is the target tissue assigned in skeletal dosimetry models for assessment of stochastic effects (leukemia induction) as well as tissue reactions (marrow toxicity). Active marrow, however, is in reality a surrogate tissue region for specific cell populations, namely the hematopoietic stem and progenitor cells. Present models of active marrow dosimetry implicitly assume that these cells are uniformly localized throughout the marrow spaces of trabecular spongiosa.
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