4.8 Article

Efficient discrimination of transplutonium actinides by in vivo models

Journal

CHEMICAL SCIENCE
Volume 12, Issue 14, Pages 5295-5301

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc06610a

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This study investigated the biodistribution and excretion profiles of four transplutonium actinides in a small animal model, as well as the effects of two therapeutic chelators on these elements. The results showed element-dependent organ deposition patterns, with lower atomic number radionuclides exhibiting higher accumulation ratios in certain organs. Furthermore, treatment with the therapeutic agent significantly decreased the metal content in multiple organs. The systematic comparison of radionuclide biodistributions may offer insights for the design of new bio-inspired chelating systems with improved sequestration and separation performance.
Transplutonium actinides are among the heaviest elements whose macroscale chemical properties can be experimentally tested. Being scarce and hazardous, their chemistry is rather unexplored, and they have traditionally been considered a rather homogeneous group, with most of their characteristics extrapolated from lanthanide surrogates. Newly emerged applications for these elements, combined with their persistent presence in nuclear waste, however, call for a better understanding of their behavior in complex living systems. In this work, we explored the biodistribution and excretion profiles of four transplutonium actinides (Cm-248, Bk-249, Cf-249 and Es-253) in a small animal model, and evaluated their in vivo sequestration and decorporation by two therapeutic chelators, diethylenetriamine pentaacetic acid and 3,4,3-LI(1,2-HOPO). Notably, the organ deposition patterns of those transplutonium actinides were element-dependent, particularly in the liver and skeleton, where lower atomic number radionuclides showed up to 7-fold larger liver/skeleton accumulation ratios. Nevertheless, the metal content in multiple organs was significantly decreased for all tested actinides, particularly in the liver, after administering the therapeutic agent 3,4,3-LI(1,2-HOPO) post-contamination. Lastly, the systematic comparison of the radionuclide biodistributions showed discernibly element-dependent organ depositions, which may provide insights into design rules for new bio-inspired chelating systems with high sequestration and separation performance.

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