Abstract
Purpose: This manuscript compares the behavior of monomeric 239Pu4+-citrate injected intravenously in rats and dogs with a comparison of available humans’ data.
Material and methods: The experimental design for these two studies consisted of eight groups sacrificed at predetermined time-points post exposure. All organs and tissues as well as daily urinary and fecal excretion were analyzed.
Results: Liver and skeleton were the organs with the highest 239Pu uptake in both species; 76% in dogs and 70% in rats at 24 hours (h) post IV administration. By the end of the study (28 days, d), the activity in skeleton and liver was 85% in dogs and 65% in rats. The urinary excretion function seems to be similar for rats, dogs and humans but the daily fecal to urinary excretion ratio differs between species.
Conclusion: A rapid clearance from the liver of rats was observed compared to dogs. Skeleton-to-liver ratios are variable between species. Urinary and fecal excretion patterns for dogs are consistent with human data, indicating that dogs seem to represent better the 239Pu behavior in humans. The data confirm that the better animal model to evaluate the efficacy of 239Pu chelating compounds is the canine model.
Acknowledgements
The work described here is being supported by the U. S. National Institute of Allergy and Infectious Diseases, NIH, under contract HHSN272201000046C, through a subcontract with the University of Maryland Center Against Radiological Threats (MCART).
Declaration of interest
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.