3.8 Article

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

Journal

EJNMMI RADIOPHARMACY AND CHEMISTRY
Volume 6, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1186/s41181-020-00114-9

Keywords

Gallium-68; Cyclotron; Accelerator; DOTATATE; PSMA-11; Solid target; Targetry

Funding

  1. Department of Nuclear Medicine, Odense University Hospital

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In response to the increasing clinical demand for gallium-68, a high-yield, automated method has been developed for producing multi-Curie levels of [Ga-68]GaCl3 from solid zinc-68 targets. This method led to record-high purified gallium-68 activities and successful labelling of PSMA-11 and DOTATATE, showing promising results for clinical use in terms of quality control.
BackgroundWith increasing clinical demand for gallium-68, commercial germanium-68/gallium-68 ([Ge-68]Ge/[Ga-68]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 [Ga-68]GaCl3 from solid zinc-68 targets and subsequent labelling to produce clinical-grade [Ga-68]Ga-PSMA-11 and [Ga-68]Ga-DOTATATE.ResultsEnriched zinc-68 targets were irradiated at up to 80 mu A with 13 MeV protons for 120 min; repeatedly producing up to 194 GBq (5.24 Ci) of purified gallium-68 in the form of [Ga-68]GaCl3 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 [Ga-68]GaCl3 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 [Ga-68]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.ConclusionsWe have developed a high-yielding, automated method for the production of very high amounts of [Ga-68]GaCl3, 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 [Ga-68]GaCl3 for radiolabelling and [Ga-68]Ga-PSMA-11 are promising for clinical use.

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