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Multi-curie production of gallium-68 on a biomedical cyclotron and automated radiolabelling of PSMA-11 and DOTATATE

BACKGROUND: With increasing clinical demand for gallium-68, commercial germanium-68/gallium-68 ([(68)Ge]Ge/[(68)Ga]Ga) generators are incapable of supplying sufficient amounts of the short-lived daughter isotope. In this study, we demonstrate a high-yield, automated method for producing multi-Curie...

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Detalles Bibliográficos
Autores principales: Thisgaard, Helge, Kumlin, Joel, Langkjær, Niels, Chua, Jansen, Hook, Brian, Jensen, Mikael, Kassaian, Amir, Zeisler, Stefan, Borjian, Sogol, Cross, Michael, Schaffer, Paul, Dam, Johan Hygum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790954/
https://www.ncbi.nlm.nih.gov/pubmed/33411034
http://dx.doi.org/10.1186/s41181-020-00114-9
Descripción
Sumario:BACKGROUND: With increasing clinical demand for gallium-68, commercial germanium-68/gallium-68 ([(68)Ge]Ge/[(68)Ga]Ga) generators are incapable of supplying sufficient amounts of the short-lived daughter isotope. In this study, we demonstrate a high-yield, automated method for producing multi-Curie levels of [(68)Ga]GaCl(3) from solid zinc-68 targets and subsequent labelling to produce clinical-grade [(68)Ga]Ga-PSMA-11 and [(68)Ga]Ga-DOTATATE. RESULTS: Enriched zinc-68 targets were irradiated at up to 80 µA with 13 MeV protons for 120 min; repeatedly producing up to 194 GBq (5.24 Ci) of purified gallium-68 in the form of [(68)Ga]GaCl(3) at the end of purification (EOP) from an expected > 370 GBq (> 10 Ci) at end of bombardment. A fully automated dissolution/separation process was completed in 35 min. Isolated product was analysed according to the Ph. Eur. monograph for accelerator produced [(68)Ga]GaCl(3) and found to comply with all specifications. In every instance, the radiochemical purity exceeded 99.9% and importantly, the radionuclidic purity was sufficient to allow for a shelf-life of up to 7 h based on this metric alone. Fully automated production of up to 72.2 GBq [(68)Ga]Ga-PSMA-11 was performed, providing a product with high radiochemical purity (> 98.2%) and very high apparent molar activities of up to 722 MBq/nmol. Further, manual radiolabelling of up to 3.2 GBq DOTATATE was performed in high yields (> 95%) and with apparent molar activities (9–25 MBq/nmol) sufficient for clinical use. CONCLUSIONS: We have developed a high-yielding, automated method for the production of very high amounts of [(68)Ga]GaCl(3), sufficient to supply proximal radiopharmacies. The reported method led to record-high purified gallium-68 activities (194 GBq at end of purification) and subsequent labelling of PSMA-11 and DOTATATE. The process was highly automated from irradiation through to formulation of the product, and as such comprised a high level of radiation protection. The quality control results obtained for both [(68)Ga]GaCl(3) for radiolabelling and [(68)Ga]Ga-PSMA-11 are promising for clinical use.