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<sup>232</sup>Th-Spallation-Produced <sup>225</sup>Ac with Reduced <sup>227</sup>Ac Content

78

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44

References

2020

Year

Abstract

Recent clinical results have demonstrated remarkable treatment responses of late-stage cancer patients when treated with alpha-emitting radionuclides such as actinium-225 (<sup>225</sup>Ac). The resulting intense global effort to produce greater quantities of <sup>225</sup>Ac has triggered a number of emerging technologies to produce this rare, yet important, radionuclide. Accelerator-based methods for increasing global <sup>225</sup>Ac production capacity have focused on the high energy (>100 MeV) proton irradiation of thorium, despite the coproduction of the undesirable <sup>227</sup>Ac byproduct at 0.1-0.3% of the <sup>225</sup>Ac activity. We at TRIUMF have developed a process for the production of a <sup>225</sup>Ra/<sup>225</sup>Ac generator from irradiated thorium that results in an <sup>225</sup>Ac product with reduced <sup>227</sup>Ac content. <sup>225</sup>Ac was separated from irradiated thorium and coproduced radioactive spallation and fission products using a thorium peroxide precipitation method followed by cation exchange and extraction chromatography. Stable and radioactive tracer studies demonstrated the ability of this method to separate Ac from most other elements, providing a directly produced Ac product with measured <sup>227</sup>Ac content of (0.15 ± 0.04)%. A second, indirectly produced Ac product with <sup>227</sup>Ac content of <7.5 × 10<sup>-5</sup>% is obtained by repeating the final extraction chromatography step with the <sup>225</sup>Ra-containing fraction. The <sup>225</sup>Ra-derived <sup>225</sup>Ac showed similar or improved quality compared to the initial, directly produced <sup>225</sup>Ac product in terms of chemical purity and radiolabeling capability, the latter of which was comparable with other <sup>225</sup>Ac sources reported in the literature.

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