A new concept for the production of C-labelled radiotracers.

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-[C]choline, L-S-methyl-[C]methionine and [C]acetate.

Results: The target gas purification of cyclotron produced [C]CO and subsequent conversion to [C]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-[C]choline and L-S-methyl-[C]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 [C]MeI. After 18 min N-methyl-[C]choline was isolated with 52% decay corrected yield and a radiochemical purity of > 99%. For L-S-methyl-[C]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 [C]acetate synthesis. The disposable unit was filled with 1 mL MeMgCl (0.75 M) in tetrahydrofuran (THF) bevore [C]CO was passed through. After complete release of [C]CO 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 [C]CO before dispensing. Under these conditions the total reaction time was 18 ± 2 min and pure [C]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-[C]choline, L-S-methyl-[C]methionine and [C]acetate.