Wickstrøm Torild, Clarke Alan, Gausemel Ingvil, Horn Eric, Jørgensen Karina, Khan Imtiaz, Mantzilas Dimitrios, Rajanayagam Thanushan, in 't Veld Dirk-Jan, Trigg William
GE Healthcare, Oslo, Norway.
J Labelled Comp Radiopharm. 2014 Jan;57(1):42-8. doi: 10.1002/jlcr.3112. Epub 2013 Sep 23.
The level of the translocator protein (TSPO) increases dramatically in microglial cells when the cells are activated in response to neuronal injury and insult. The radiotracer [(18) F]GE-180 binds selectively and with high affinity to TSPO and can therefore be used to measure neuroinflammation in a variety of disease states. An optimized, automated synthesis of [(18) F]GE-180 has been developed for the GE FASTlab™ synthesizer. The entire process takes place on the single-use cassette. The radiolabelling is performed by nucleophilic fluorination of the S- enantiomer mesylate precursor. The crude product is purified post-radiolabelling using two solid-phase extraction cartridges integrated on the cassette. Experimental design and multivariate data analysis were used to assess the robustness, and critical steps were optimized with respect to efficacy and quality. The average radiochemical yield is 48% (RSD 6%, non-decay corrected), and the synthesis time including purification is approximately 43 min. The radiochemical purity is ≥95% for radioactive concentration ≤1100 MBq/mL. The total amount of precursor-related chemical impurities is 1-2 µg/mL. The use of solid-phase extraction purification results in a robust GMP compliant process with a product of high chemical and radiochemical purity and consistent performance across positron emission tomography (PET) centers.
当小胶质细胞因神经元损伤和刺激而被激活时,转位蛋白(TSPO)水平会显著升高。放射性示踪剂[(18)F]GE-180能选择性且高亲和力地与TSPO结合,因此可用于测量多种疾病状态下的神经炎症。已为GE FASTlab™合成仪开发了一种优化的[(18)F]GE-180自动化合成方法。整个过程在一次性试剂盒上进行。放射性标记通过S-对映体甲磺酸盐前体的亲核氟化反应进行。粗产物在放射性标记后使用试剂盒上集成的两个固相萃取柱进行纯化。采用实验设计和多变量数据分析来评估稳健性,并针对效率和质量对关键步骤进行了优化。平均放射化学产率为48%(相对标准偏差6%,未进行衰变校正),包括纯化在内的合成时间约为43分钟。对于放射性浓度≤1100 MBq/mL,放射化学纯度≥95%。前体相关化学杂质的总量为1 - 2 μg/mL。使用固相萃取纯化可实现符合GMP的稳健过程,得到化学纯度和放射化学纯度高且在正电子发射断层扫描(PET)中心性能一致的产品。