Abstract

The early retention and distribution of 239Pu in the beagle were compared following intravenous administration of 239Pu(IV) as the transferrin complex (Pu-Tf), as a plutonium complex in citrate buffer (Pu-Cit) of pH 3.5 and as a particulate Pu(IV) in colloidal form (Pu-P). The early distribution and retention of Pu(IV) at 14 days after injection of Pu-citrate and pu-transferrin were indistinguishable. There was a difference in urinary excretion patterns. Deposition, microdistribution and retention after administration of a suspension of particulate Pu(IV) differed greatly from those seen in dogs injected with true solutions of plutonium. After injection of Pu-Tf or Pu-Cit, the nuclide was cleared from circulation at a slow rate. Approximately 30% was deposited in the liver, ∼50% in the skeleton and ∼2% in other soft tissues. Pu-P left the circulation at a very fast rate, ∼70% was deposited in the liver, with only 2% in the bone and ∼24% in other soft tissue. Only an insignificant fraction of the injected Pu-P was excreted. In the liver, the microdistribution after injection of Pu-Tf and Pu-Cit was uniform and Pu(IV) was associated first with soluble protein and later transferred to subcellular liver particles. After injection of Pu-P the microdistribution was heterogeneous; most of the Pu(IV) was located in R. E. cells and little was associated with soluble proteins. After injection of Pu-Cit and Pu-Tf, Pu(IV) was found on bone surfaces, whereas after injection of Pu-P, the small amount of Pu(IV) present was located exclusively in macrophages of the bone marrow.

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