4.3 Article

Demystifying solid targets: Simple and rapid distribution-scale production of [68Ga]GaCl3 and [68Ga]Ga-PSMA-11

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NUCLEAR MEDICINE AND BIOLOGY
卷 104, 期 -, 页码 -

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2021.10.002

关键词

Ga-68; [Ga-68]Ga-PSMA-11; Solid target system; Automated /automation; Positron emission tomography (PET); Apparent molar activity (AMA)

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The study focused on a fully automated solid target production and purification process with a simplified chemistry execution using a single time-list. High activity productions of [Ga-68]GaCl3 achieved a high purification yield with good radiochemical yields, while [Ga-68]Ga-PSMA-11 productions also showed promising results in terms of yield and purity.
Background: As the demand for Ga-68 continues to grow, there is increasing interest in single-to-multi-Curie production quantities of both [Ga-68]GaCl3 and tracers such as [Ga-68]Ga-PSMA-11. While such quantities are possible with solid targets, this implementation is often challenging as it typically requires significant site expertise for solid target processing and careful operator-dependent synchronization of multiple independent time-sensitive chemistry steps. Herein we focus on a fully automated solid target production and purification process whereby we avoid the need for tongs/tele-pliers, and have simplified the chemistry by implementing a single sequence (i.e. time-list) to execute cassette-based dissolution, purification, and labeling. Methods: Electroplated Zn-68 was irradiated in a PETtrace prototype automated solid target system. Following irradiation, and using a single FASTlab time-list, the Zn-68 was automatically dissolved with HCl/H2O2 and purified as [Ga-68]GaCl3 using a combination of resins (ZRJTK400, A8, TK200: Triskem). For select experiments, [Ga-68]Ga-PSMA-11 was also produced on the same cassette/single time-list (N = 4). or, by kit labeling (N = 1). Efforts focused towards on-cassette production of [Ga-68]GaCl3 strived to maximize activity and quality, whereas efforts focused towards on-cassette production of [Ga-68]Ga-PSMA-11 aimed at limiting the entire production cycle to 1 h including the irradiation time (i.e. start-of-bombardment -> end-of-synthesis [EOS]). Results: For the high activity triplicate [Ga-68]GaCl3 productions (i.e. 80 mu A, 102 min, 216 +/- 10 mg), [Ga-68]GaCl3 was purified (end-of-bombardment -> end-of-purification [EOP]) in similar to 28 min with activity yields of 181 +/- 8 GBq at EOP and average radiochemical yields of 66 +/- 5%. Average AMAs of 2.26 +/- 0.16 TBq/mu mol using DOTA (N = 3) and 12.00 TBq/mu mol using HBED (PSMA-11) (N = 1) at EOP were measured. For the single kit test, (80 mu A, 120 min, 263 mg Zn-68) for which 18 mg ascorbic acid was added to the buffer, 199 GBq of [Ga-68]Ga-PSMA-11 was successfully produced (thin layer chromatography-based radiochemical purity >99% at 6 h EOS). Finally, for efforts focused at expedient [Ga-68]Ga-PSMA-11, up to 42 GBq [Ga-68]Ga-PSMA-11 with a radiochemical yield of 51.2% was produced in 63 min. including beamtime, using 220 mg of Zn-68 as target material. Conclusion: With the goal of simplifying solid target production and purification efforts, automated methods using single-use, cassette-based approaches for rapid, large-scale, single time-list production of [Ga-68]GaCl3 and [Ga-68]Ga-PSMA-11 were developed. These methods were simple to execute and yielded high quality multi-Curie levels of both [Ga-68]GaCl3 and [Ga-68]Ga-PSMA-11. (C) 2021 The Authors. Published by Elsevier Inc.

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