Fine-tuning of the automated [18F]PSMA-1007 radiosynthesis

被引:8
|
作者
Shamni, Ofer [1 ]
Nebeling, Bruno [2 ]
Grievink, Hilbert [1 ]
Mishani, Eyal [1 ]
机构
[1] Hadassah Hebrew Univ Hosp, Hadassah Med Org, Cyclotron Radiochem MicroPET Unit, IL-91120 Jerusalem, Israel
[2] Synthra GmbH, Hamburg, Germany
关键词
F-18]PSMA-1007; fluorine-18; PET; prostate cancer; PSMA; PROSTATE-CANCER; PRECLINICAL EVALUATION; RADIATION-DOSIMETRY; MEMBRANE ANTIGEN; BIODISTRIBUTION; F-18-PSMA-1007; PET/CT; F-18-DCFPYL; LIGAND;
D O I
10.1002/jlcr.3732
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Radiolabeled prostate-specific membrane antigen (PSMA) targeting PET-tracers have become desirable radiopharmaceuticals for the imaging of prostate cancer (PC). Recently, the PET radiotracer [F-18]PSMA-1007 was introduced as an alternative to [Ga-68]Ga-PSMA-11, for staging and diagnosing biochemically recurrent PC. We incorporated a one-step procedure for [F-18]PSMA-1007 radiosynthesis, using both Synthra RNplus and GE TRACERlab FxFN automated modules, in accordance with the recently described radiolabeling procedure. Although the adapted [F-18]PSMA-1007 synthesis resulted in repeatable radiochemical yields (55 +/- 5%, NDC), suboptimal radiochemical purities of 87 +/- 8% were obtained using both modules. As described here, modifications made to the radiolabeling and the solid-phase extraction purification steps reduced synthesis time to 32 minutes and improved radiochemical purity to 96.10%, using both modules, without shearing the radiochemical yield.
引用
收藏
页码:252 / 258
页数:7
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