Atanasova Lazareva Marija, Chochevska Maja, Kolevska Katerina, Velickovska Maja, Jolevski Filip, Apostolova Paulina, Ugrinska Ana, Janevik-Ivanovska Emilija
University Institute of Positron Emission Tomography, Skopje, Republic of North Macedonia.
Faculty of Medical Sciences, Goce Delcev University, Stip, Republic of North Macedonia.
EJNMMI Radiopharm Chem. 2025 Feb 4;10(1):8. doi: 10.1186/s41181-025-00329-8.
Sodium F-fluoride for injection can be easily cyclotron-produced and purified, as a simple inorganic salt, by adsorption/desorption onto an anion-exchange cartridge and then dispensed for clinical use. Since the clinical demand for this radiopharmaceutical is constantly increasing, this study aimed to design and develop a simple, fully automated method for the in-house, rapid, and efficient processing and dispensing of injectable solutions of Sodium F-fluoride without the need of a synthesis module and disposable kit, but using only the dispensing unit.
A new simple method for the efficient routine production of injectable solutions of [F]NaF was developed through a straightforward modification of the commercial dispenser Clio (Comecer S.p.A., Italy) and without the need of a synthesis module. The full production, processing and dispensing of [F]NaF were entirely carried out on the same batch using only the dispensing module. Process validation was carried according to GMP guidelines to ensure consistency of [F]NaF quality with international standards. The final radiopharmaceutical met all quality criteria specified by Ph. Eur. and chemical, radionuclidic and radiochemical impurities were significantly below the required limits.
A new simple and reliable procedure developed for the preparation and dispensing of injectable [F]NaF in less than 10 min with a radiochemical yield > 97% (decay corrected) has been successfully developed. Notably, the proposed method also allows the preparation of [F]NaF using the residual fluorine-18 activity remaining after a [F]FDG production run, thus making it immediately accessible to patients for further PET imaging investigations.
注射用氟化钠可以很容易地通过回旋加速器生产并纯化,作为一种简单的无机盐,通过在阴离子交换柱上吸附/解吸,然后配制成临床用制剂。由于这种放射性药物的临床需求不断增加,本研究旨在设计并开发一种简单的全自动方法,用于在内部快速高效地处理和配制注射用氟化钠溶液,无需合成模块和一次性试剂盒,仅使用配液单元即可。
通过对商用配液器Clio(意大利Comecer S.p.A.公司)进行直接改造,开发出一种高效常规生产注射用[F]NaF溶液的新方法,无需合成模块。[F]NaF的整个生产、处理和配制仅使用配液模块在同一批次中完全完成。根据GMP指南进行工艺验证,以确保[F]NaF质量与国际标准一致。最终的放射性药物符合欧洲药典规定的所有质量标准,化学、放射性核素和放射化学杂质显著低于规定限度。
已成功开发出一种新的简单可靠的程序,用于在不到10分钟内制备和配制注射用[F]NaF,放射化学产率>97%(衰变校正)。值得注意的是,所提出的方法还允许利用[F]FDG生产运行后剩余的氟-18活性制备[F]NaF,从而使患者能够立即进行进一步的PET成像检查。