TY - JOUR
AU - Krapf, Philipp
AU - Wicher, Thomas
AU - Zlatopolskiy, Boris
AU - Ermert, Johannes
AU - Neumaier, Bernd
TI - Fully automated production of (((S)-1-carboxy-5-(6-([18F]fluoro)-2-methoxynicotinamido)pentyl)carbamoyl)-l-glutamic acid ([18F]JKPSMA-7
JO - Pharmaceuticals
VL - 18
IS - 1
SN - 1424-8247
CY - Basel
PB - MDPI
M1 - FZJ-2025-00361
SP - 119 -
PY - 2025
AB - The radiotracer [18F]JK-PSMA-7, a prostate cancer imaging agent for positron emission tomography (PET), was previously synthesized by indirect radiofluorination using an 18F-labeled active ester as a prosthetic group, which had to be isolated and purified before it could be linked to the pharmacologically active Lys-urea-Glu motif. Although this procedure could be automated on two-reactor modules like the GE TRACERLab FX2N (FXN) to afford the tracer in modest radiochemical yields (RCY) of 18–25%, it is unsuitable for cassette-based systems with a single reactor. Methods: To simplify implementation on an automated synthesis module, the radiosynthesis of [18F]JK-PSMA-7 was devised as a one-pot, two-step reaction. The new method is based on direct (“late-stage”) radiofluorination of an appropriate onium triflate precursor and subsequent deprotection with ortho-phosphoric acid. It was successfully established on the cassette-based Trasis AllInOne (AIO) module. Results: Overall, the new protocol enabled the production of [18F]JK-PSMA-7 in activity yields of 39 ± 4%(RCY = 58%) with an overall synthesis time of about 1 h. In a single production run with an initial activity of 36-43 GBq, 13-19 GBq of [18F]JK-PSMA-7 with a radiochemical purity of >99%was obtained. Conclusions: We have established a highly reliable, GMP-compliant process for the automated radiosynthesis of [18F]JK-PSMA-7 on the Trasis AllinOne (AIO) synthesizer, ensuring consistent and efficient production of this radioligand.
LB - PUB:(DE-HGF)16
C6 - 39861180
UR - <Go to ISI:>//WOS:001405742900001
DO - DOI:10.3390/ph18010119
UR - https://juser.fz-juelich.de/record/1035303
ER -