Rapid fabrication and dissolution of pressed 58Ni/Mg matrix targets for 55Co production

IF 4.4 Q1 CHEMISTRY, INORGANIC & NUCLEAR EJNMMI Radiopharmacy and Chemistry Pub Date : 2025-01-21 DOI:10.1186/s41181-024-00324-5
Jonathan Siikanen, Stefan Milton, Klas Bratteby, Wilson Lin, Jonathan W. Engle, Emma Jussing, Thuy A. Tran
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Abstract

Background

Beyond the use of conventional short-lived PET radionuclides, there is a growing interest in tracking larger biomolecules and exploring radiotheranostic applications. One promising option for imaging medium-sized molecules and peptides is ⁵⁵Co (T₁/₂ = 17.5 h, β⁺ = 76%), which enables imaging of new and already established tracers with blood circulation of several hours. Additionally, ⁵⁵Co can be paired with the Auger-Meitner emitter 58mCo (T₁/₂ = 9 h, 100% IC) for radiotheranostic applications. Here we report on 55Co production via the 58Ni(p,α)55Co reaction channel using pressed 58Ni and Mg matrix targets.

Results

This set up is capable to produce and isolate 240 ± 20 MBq [55Co]Co+ 2 (80% RCY) with 4 ml 0.25 M HEPES at 35 min post End Of Bombardment for 3 h, 25 µA protons irradiation. The RNP of the eluate is 99.98 ± 0.014% as measured 2 h & 17 h post EOB. AMA was determined to 1.5 ± 0.5 GBq/µmol [55Co]Co-DOTA at EOB. Mg dissolves rapidly in the acid mixture, leaving behind a porous, sponge-like Ni matrix increasing the surface area of the Ni and therefore accelerating the dissolution.

Conclusion

We present a novel, simple, and rapid method to produce ⁵⁵Co with pressed ⁵⁸Ni/Mg matrix targets enabling faster target fabrication and dissolution. By using a simple hydraulic press, mechanically stable target coins useful for solid target irradiation are fabricated within 5 min and can be dissolved in 10 min at room temperature. The foils remain intact after irradiation and can endure irradiation conditions providing sufficient activity (> 200 MBq) for clinical doses. The method presented here using Mg as a support metal for fixation of the actual target material into target coins is applicable for other target combinations as well. Using Mg as a support metal is suitable due to its thermal conductivity, low activation, minimal impact on purification chemistry, softness, ductility, and rapid dissolution in acid.

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用于55Co生产的58Ni/Mg基体靶材的快速制备和溶解
除了使用传统的短寿命PET放射性核素外,人们对追踪较大的生物分子和探索放射治疗应用的兴趣日益浓厚。对中等大小的分子和多肽进行成像的一个很有前途的选择是5 - 5 + Co (T₁/ 2 = 17.5 h, β⁺= 76%),它可以对新的和已经建立的血液循环数小时的示踪剂进行成像。此外,可以与奥格-迈特纳发射器58mCo (T₁/ 2 = 9 h, 100% IC)配对,用于放射治疗应用。在这里,我们报告了58Ni(p,α)55Co反应通道使用压制58Ni和Mg基体靶生产55Co。结果该装置在轰击结束后35 min, 25µA质子照射3 h,用4 ml 0.25 M HEPES可产生并分离240±20 MBq [55Co]Co+ 2 (80% RCY)。2 h时,洗脱液的RNP为99.98±0.014%;EOB后17小时。在EOB时测定AMA为1.5±0.5 GBq/µmol [55Co]Co-DOTA。Mg在酸性混合物中迅速溶解,留下多孔的海绵状镍基体,增加了Ni的表面积,从而加速了溶解。我们提出了一种新颖、简单、快速的方法,利用压制的镍/镁基靶材制备出了更快的靶材。通过使用简单的液压机,在5分钟内制造出可用于固体靶照射的机械稳定靶币,并可在室温下在10分钟内溶解。箔片在照射后保持完整,并能承受照射条件,为临床剂量提供足够的活性(200 MBq)。本文采用Mg作为支撑金属将实际靶材固定到靶币中的方法也适用于其他靶组合。使用镁作为支撑金属是合适的,因为它的导热性,低活化,对净化化学的影响最小,柔软,延展性好,在酸中溶解快。
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来源期刊
CiteScore
7.20
自引率
8.70%
发文量
30
审稿时长
5 weeks
期刊最新文献
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