Johnson Jake D, Bernerd Cyril, Bruchertseifer Frank, Cocolios Thomas E, Deseyn Marie, Duchemin Charlotte, Heines Michael, Keppens Max, Lambert Laura, Meurrens Nathan, Rossel Ralf E, Stora Thierry, Bergh Viktor Van den
KU Leuven, IKS, Leuven, Belgium.
CERN, Geneva, Switzerland.
Sci Rep. 2025 Jul 2;15(1):23563. doi: 10.1038/s41598-025-02277-4.
Ac is a promising candidate medical radionuclide for targeted alpha therapy of advanced stage cancers. One of the main production pathways is the high-energy proton spallation of thorium-based targets, that requires an efficient, nuclide-selective separation method to recover Ac from hundreds of co-produced spallation and fission products. The main radioactive contaminant of concern is Ac (T = 21.8 years), that could preclude extensive medical use if not significantly suppressed. In this work, Ac samples were produced by mass separation of radioactive ion beams extracted from proton-irradiated thorium-based targets. The activity of Ac and other possible contaminants of the samples were measured using complementary gamma- and alpha-decay spectrometry methods, while Ac activity was calculated by performing alpha-decay spectrometry of recoiled progeny from the sample. Using this novel method, accurate measurement of trace Ac activity in Ac samples was performed much faster than with conventional spectrometry techniques, thanks to its 10,000-fold increase in relative sensitivity. The end of collection activity ratio of Ac to Ac in two samples from irradiated targets were determined to be [Formula: see text] and [Formula: see text] respectively, three orders of magnitude below the Ac activity in Ac products obtained through radiochemical separation. The high separation factor of Ac over Ac suggests the suitability of mass-separated accelerator-based Ac for medical use.
锕是晚期癌症靶向α治疗中一种很有前景的候选医用放射性核素。其主要生产途径之一是基于钍靶的高能质子散裂,这需要一种高效、核素选择性的分离方法,以便从数百种共同产生的散裂和裂变产物中回收锕。主要关注的放射性污染物是锕-227(半衰期T = 21.8年),如果不能显著抑制,可能会妨碍其广泛的医学应用。在这项工作中,通过对从质子辐照钍基靶中提取的放射性离子束进行质量分离来制备锕样品。使用互补的γ衰变和α衰变光谱法测量样品中锕和其他可能污染物的活度,同时通过对样品反冲子代进行α衰变光谱法来计算锕的活度。使用这种新方法,由于其相对灵敏度提高了10000倍,对锕样品中痕量锕活度的准确测量比传统光谱技术快得多。确定了来自辐照靶的两个样品中锕-225与锕-227的收集活度终比分别为[公式:见原文]和[公式:见原文],比通过放射化学分离获得的锕-225产品中的锕-227活度低三个数量级。锕-225相对于锕-227的高分离因子表明基于加速器质量分离的锕-225适用于医学用途。