Development of 225Ac/213Bi generator based on α-ZrP-PAN composite for targeted alpha therapy

IF 3.6 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Lukáš Ondrák , Kateřina Ondrák Fialová , Michal Sakmár , Martin Vlk , Frank Bruchertseifer , Alfred Morgenstern , Ján Kozempel
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Abstract

Background

Radioligand therapy using alpha emitters has gained more and more prominence in the last decade. Despite continued efforts to identify new appropriate radionuclides, the combination of 225Ac/213Bi remains among the most promising. Bismuth-213 has been employed in clinical trials in combination with appropriate vectors to treat patients with various forms of cancer, such as leukaemia, bladder cancer, neuroendocrine tumours, melanomas, gliomas, or lymphomas. However, the half-life of 213Bi (T½ = 46 min) implies that its availability for clinical use is limited to hospitals possessing a 225Ac/213Bi radionuclide generator, which is still predominantly scarce. We investigated a new Ac/Bi generator system based on using the composite sorbent α-ZrP-PAN (zirconium(IV) phosphate as active component and polyacrylonitrile as matrix). The developed 225Ac/213Bi generator was subjected to long-term testing after its development. The elution profile was determined and the elution yield, the contamination of the eluate with the parent 225Ac and the contamination of the eluate with the column material were monitored over time.

Results

The high activity (75 MBq of parent 225Ac) generator with a length of 75 mm and a diameter of 4 mm containing the composite sorbent α-ZrP-PAN with a particle size of 0.8 to 1.0 mm as the stationary phase, eluted with a mixture of 10 mM DTPA in 5 mM nitric acid, provided 213Bi with yields ranging from 77 % to 96 % in 2.8 mL of eluate, with parent 225Ac contamination in the order of 10−3 %, up to twenty days of use.

Conclusion

All the results of the monitored parameters indicate that the composite sorbent α-ZrP-PAN based separation system for the elution of 213Bi is a very promising and functional solution.

Abstract Image

开发基于 α-ZrP-PAN 复合材料的 225Ac/213Bi 发生器,用于α靶向治疗
背景使用α发射体的放射性配体疗法在过去十年中越来越受到重视。尽管人们一直在努力寻找新的合适放射性核素,但 225Ac/213Bi 的组合仍然是最有前途的。在临床试验中,铋-213 已与适当的载体结合,用于治疗各种癌症患者,如白血病、膀胱癌、神经内分泌肿瘤、黑色素瘤、胶质瘤或淋巴瘤。然而,213Bi 的半衰期(T½ = 46 分钟)意味着其临床应用仅限于拥有 225Ac/213Bi 放射性核素发生器的医院,而这种放射性核素发生器仍然非常稀缺。我们研究了一种新的 Ac/Bi 发生器系统,其基础是使用复合吸附剂 α-ZrP-PAN(以磷酸锆(IV)为活性成分,聚丙烯腈为基质)。所开发的 225Ac/213Bi 发生器在开发后进行了长期测试。结果高活性(75 MBq 母体 225Ac)发生器长度为 75 毫米,直径为 4 毫米,含有粒径为 0.8 至 1.0 毫米的复合吸附剂 α-ZrP-PAN。结论 所有监测参数的结果表明,基于复合吸附剂 α-ZrP-PAN 的 213Bi 洗脱分离系统是一种非常有前途的功能性解决方案。
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来源期刊
Nuclear medicine and biology
Nuclear medicine and biology 医学-核医学
CiteScore
6.00
自引率
9.70%
发文量
479
审稿时长
51 days
期刊介绍: Nuclear Medicine and Biology publishes original research addressing all aspects of radiopharmaceutical science: synthesis, in vitro and ex vivo studies, in vivo biodistribution by dissection or imaging, radiopharmacology, radiopharmacy, and translational clinical studies of new targeted radiotracers. The importance of the target to an unmet clinical need should be the first consideration. If the synthesis of a new radiopharmaceutical is submitted without in vitro or in vivo data, then the uniqueness of the chemistry must be emphasized. These multidisciplinary studies should validate the mechanism of localization whether the probe is based on binding to a receptor, enzyme, tumor antigen, or another well-defined target. The studies should be aimed at evaluating how the chemical and radiopharmaceutical properties affect pharmacokinetics, pharmacodynamics, or therapeutic efficacy. Ideally, the study would address the sensitivity of the probe to changes in disease or treatment, although studies validating mechanism alone are acceptable. Radiopharmacy practice, addressing the issues of preparation, automation, quality control, dispensing, and regulations applicable to qualification and administration of radiopharmaceuticals to humans, is an important aspect of the developmental process, but only if the study has a significant impact on the field. Contributions on the subject of therapeutic radiopharmaceuticals also are appropriate provided that the specificity of labeled compound localization and therapeutic effect have been addressed.
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