A new concept for the production of 11C-labelled radiotracers
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Open Access
- 28 March 2022
- journal article
- research article
- Published by Springer Nature in EJNMMI Radiopharmacy and Chemistry
- Vol. 7 (1) , 1-14
Abstract
Background: The GMP-compliant production of radiopharmaceuticals has been performed using disposable units (cassettes) with a dedicated synthesis module. To expand this “plug ‘n’ synthesize” principle to a broader scope of modules we developed a pressure controlled setup that offers an alternative to the usual stepper motor controlled rotary valves. The new concept was successfully applied to the synthesis of N-methyl-[11C]choline, L-S-methyl-[11C]methionine and [11C]acetate. Results: The target gas purification of cyclotron produced [11C]CO2 and subsequent conversion to [11C]MeI was carried out on a TRACERlab Fx C Pro module. The labelling reactions were controlled with a TRACERlab Fx FE module. With the presented modular principle we were able to produce N-methyl-[11C]choline and L-S-methyl-[11C]methionine by loading a reaction loop with neat N,N'-dimethylaminoethanol (DMAE) or an ethanol/water mixture of NaOH and L-homocysteine (L-HC), respectively and a subsequent reaction with [11C]MeI. After 18 min N-methyl-[11C]choline was isolated with 52% decay corrected yield and a radiochemical purity of > 99%. For L-S-methyl-[11C]methionine the total reaction time was 19 min reaction, yielding 25% of pure product (> 97%). The reactor design was used as an exemplary model for the technically challenging [11C]acetate synthesis. The disposable unit was filled with 1 mL MeMgCl (0.75 M) in tetrahydrofuran (THF) bevore [11C]CO2 was passed through. After complete release of [11C]CO2 the reaction mixture was quenched with water and guided through a series of ion exchangers (H+, Ag+ and OH−). The product was retained on a strong anion exchanger, washed with water and finally extracted with saline. The product mixture was acidified and degassed to separate excess [11C]CO2 before dispensing. Under these conditions the total reaction time was 18 ± 2 min and pure [11C]acetate (n = 10) was isolated with a decay corrected yield of 51 ± 5%. Conclusion: Herein, we described a novel single use unit for the synthesis of carbon-11 labelled tracers for preclinical and clinical applications of N-methyl-[11C]choline, L-S-methyl-[11C]methionine and [11C]acetate.Keywords
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Funding Information
- Universitätsklinikum Würzburg
This publication has 38 references indexed in Scilit:
- 2039 IMPACT OF 11C-CHOLINE PET/CT SCAN ON DETECTION OF RECURRENT PROSTATE CANCER IN MEN WITH BIOCHEMICAL RECURRENCE FOLLOWING FAILED INITIAL TREATMENTJournal of Urology, 2012
- [11C]Choline PET/CT for Targeted Salvage Lymph Node Dissection in Patients with Biochemical Recurrence after Primary Curative Therapy for Prostate CancerUrologia Internationalis, 2008
- Reliability and reproducibility of N-[11C]methyl-choline and L-(S-methyl-[11C])methionine solid-phase synthesis: a useful and suitable method in clinical practiceNuclear Medicine Communications, 2008
- Detection of Lymph-Node Metastases with Integrated [11C]Choline PET/CT in Patients with PSA Failure after Radical Retropubic Prostatectomy: Results Confirmed by Open Pelvic-Retroperitoneal LymphadenectomyEuropean Urology, 2007
- Captive solvent [11C]acetate synthesis in GMP conditionsApplied Radiation and Isotopes, 2006
- New aspects on the preparation of [11C]acetate—a simple and fast approach via distillationApplied Radiation and Isotopes, 2004
- Synthesis of [11C]iodomethane by iodination of [11C]methaneApplied Radiation and Isotopes, 1997
- [11C]acetate and [11C]methionine: Improved syntheses and quality controlApplied Radiation and Isotopes, 1995
- A simple synthesis of [11C]methyl triflateInternational Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1992
- Further Experiments with Artificially Produced Radioactive SubstancesPhysical Review B, 1934