3.8 Article

Cyclotron production and radiochemical purification of terbium-155 for SPECT imaging

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SPRINGERNATURE
DOI: 10.1186/s41181-021-00153-w

关键词

Terbium-155; Matched pairs; Radiolanthanides; Theragnostics; Radionuclide production; Proton irradiation; Cyclotron; Radiochemical purification; SPECT/CT imaging

资金

  1. Swiss National Science Foundation (SNSF) [200021_188495, CRSII5_180352]
  2. European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie Grant [701647]
  3. Swiss Cancer Research Foundation [KFS-4678-02-2019-R]
  4. Swiss National Science Foundation (SNF) [200021_188495] Funding Source: Swiss National Science Foundation (SNF)

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This study demonstrated two possible production routes for high activities of terbium-155 using a cyclotron, indicating that the radionuclide is more accessible than the exclusive mass-separated method previously demonstrated. The developed radiochemical purification of terbium-155 from the target material yielded [Tb-155]TbCl3 in high chemical purity. As a result, initial cell uptake investigations, as well as SPECT/CT in vivo studies with [Tb-155]Tb-DOTATOC, were successfully performed, indicating that the chemical separation produced a product with suitable quality for preclinical studies.
Background: Terbium-155 [T-1/2 = 5.32 d, E gamma = 87 keV (32%) 105 keV (25%)] is an interesting radionuclide suitable for single photon emission computed tomography (SPECT) imaging with potential application in the diagnosis of oncological disease. It shows similar decay characteristics to the clinically established indium-111 and would be a useful substitute for the diagnosis and prospective dosimetry with biomolecules that are afterwards labeled with therapeutic radiolanthanides and pseudo-radiolanthanides, such as lutetium-177 and yttrium-90. Moreover, terbium-155 could form part of the perfect matched pair with the therapeutic radionuclide terbium-161, making the concept of true radiotheragnostics a reality. The aim of this study was the investigation of the production of terbium-155 via the Gd-155(p,n)Tb-155 and Gd-156(p,2n)Tb-155 nuclear reactions and its subsequent purification, in order to obtain a final product in quantity and quality sufficient for preclinical application. The Gd-156(p,2n)Tb-155 nuclear reaction was performed with 72 MeV protons (degraded to similar to 23 MeV), while the Gd-155(p,n)Tb-155 reaction was degraded further to similar to 10 MeV, as well as performed at an 18 MeV medical cyclotron, to demonstrate its feasibility of production. Result: The Gd-156(p,2n)Tb-155 nuclear reaction demonstrated higher production yields of up to 1.7 GBq, however, lower radionuclidic purity when compared to the final product (similar to 200 MBq) of the Gd-155(p,n)Tb-155 nuclear reaction. In particular, other radioisotopes of terbium were produced as side products. The radiochemical purification of terbium-155 from the target material was developed to provide up to 1.0 GBq product in a small volume (similar to 1 mL 0.05 M HCl), suitable for radiolabeling purposes. The high chemical purity of terbium-155 was proven by radiolabeling experiments at molar activities up to 100 MBq/nmol. SPECT/CT experiments were performed in tumor-bearing mice using [Tb-155]Tb-DOTATOC. Conclusion: This study demonstrated two possible production routes for high activities of terbium-155 using a cyclotron, indicating that the radionuclide is more accessible than the exclusive mass-separated method previously demonstrated. The developed radiochemical purification of terbium-155 from the target material yielded [Tb-155]TbCl3 in high chemical purity. As a result, initial cell uptake investigations, as well as SPECT/CT in vivo studies with [Tb-155]Tb-DOTATOC, were successfully performed, indicating that the chemical separation produced a product with suitable quality for preclinical studies.

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