Microdosimetry for leukaemogenic target cells for bone-incorporated alpha-emitting radionuclides

A. L. Austin*, B. I. Lord, Michele Ellender, Jacqueline Haines, John Harrison

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

Neutron-induced autoradiographs of femoral bone shafts taken from mice injected with 40 kBq.kg-1 239Pu, 241Am or 233U, 1, 28 or 224 days previously, were analysed morphometrically in order to present a comparison of the changing radionuclide distribution patterns. Microdosimetric methods were used to calculate localised dose rates throughout the bone marrow, and hence to those cells thought to be target cells for leukaemia induction. Initially all three radionuclides were found to be primarily deposited on the endosteal and periosteal surfaces of the bone. 241Am was additionally deposited on the surfaces of the vascular canals. 239Pu subsequently became either buried in the bone matrix or resorbed into macrophages, which by 224 days were seen to have migrated towards the central venous sinus. 241Am deposits were also present in macrophages, but to a lesser extent. In contrast uranium was not taken up into macrophages. Mean dose rates to the axial region of marrow, believed to contain the leukaemogenic target cells, were calculated for plutonium as 0.11, 0.07 and 16.78 mGy.d-1 and for americium as 0.23, 5.19 and 2.28 mGy.d-1 at 1, 28 and 224 days respectively. For uranium a dose rate of zero was calculated at all time points.

Original languageEnglish
Pages (from-to)391-394
Number of pages4
JournalRadiation Protection Dosimetry
Volume79
Issue number1-4
DOIs
Publication statusPublished - 1998

Fingerprint

Dive into the research topics of 'Microdosimetry for leukaemogenic target cells for bone-incorporated alpha-emitting radionuclides'. Together they form a unique fingerprint.

Cite this