4.3 Article

Automated radiosynthesis of 5-[11C]L-glutamine, an important tracer for glutamine utilization

Journal

NUCLEAR MEDICINE AND BIOLOGY
Volume 67, Issue -, Pages 10-14

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2018.09.002

Keywords

Radiopharmaceuticals; [C-11]Glutamine; Automated radiosynthesis; Metabolism; PET; Carbon-11

Funding

  1. Vanderbilt Ingram Cancer Center Support Grant (National Institutes of Health (NIH) National Cancer Institute (NCI)) [P30CA068485]
  2. Kleberg Foundation
  3. Vanderbilt Trans-Institutional Program (TIPS) Award
  4. Vanderbilt Digestive Disease Research Center (NIH National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)) [P30DK058404]
  5. Shared Instrumentation Grant (NIH) [1S100D019963]

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Introduction: The natural amino acid L-Glutamine (Gin) is essential for both cell growth and proliferation. In addition to glucose, cancer cells utilize Gln as a carbon source for ATP production, biosynthesis, and as a defense against reactive oxygen species. The utilization of [C-11]Gln has been previously reported as a biomarker for tissues with an elevated demand for Gln, however, the previous reports for the preparation of [C-11]Gln were found to be lacking several crucial aspects necessary for transition to human production. Namely, the presence of unreacted precursor and the use of non-commercialized, custom built, reaction platforms. Herein, we report the development and utilization of methodology for the automated production of [C-11]Gln that meets institutional criteria for human use. Methods: The preparation of [C-11]Gln was carried out on the GE FX2N platform. Briefly, after trapping of [C-11]HCN with a solution of CsHCO3 in DMF, the [C-11]CsCN was reacted with a commercially available precursor. This intermediate was then purified by HPLC and deprotected/hydrolyzed under acidic conditions. Following pH adjustment, the product was filtered to give the desired [C-11]Gln as a sterile injectable. The resulting product was then analyzed for quality assurance. Results: Automated production by this method reliably provides over 3.7 GBq (100 mCi) of [C-11]Gln. The resulting final drug product was found to have a >99% radiochemical purity, <5% of D-Gln present, no detectable impurities, and the total preparation time was roughly 45 min from the end-of-bombardment. Conclusions: A fast, reliable and efficient automated radiosynthesis was developed using a commercially available module. Purifications used throughout allow for both a radiochemically and chemically pure final product solution of [C-11]Gln. (C) 2018 Elsevier Inc. All rights reserved.

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