作为生产工艺开发的一部分,研究不同类型阴离子交换筒对[18f] naf放射性药物质量的影响

Marija Atanasova Lazareva, A. Ugrinska, E. Janevik-Ivanovska
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引用次数: 0

摘要

[18F]氟化钠放射性药物是一种无菌静脉给药溶液,用于正电子发射断层扫描(PET)骨骼可视化。[18F]氟化钠用于骨成像是在20世纪60年代早期引入的,但随着近20年来PET扫描仪的普及,这种放射性药物在临床实践中越来越多地用于骨转移的检测。[18F]NaF的生产过程包括放射性同位素[18F]F-的生产和[18F]NaF放射性药物的纯化和配方。放射性同位素[18F]F-由一个回旋加速器通过18O(p,n)18F核反应产生,然后通过阴离子交换树脂的吸附和解吸从[18O]质子辐照的水中回收[18F]F-。氟离子阴离子被捕获在阴离子交换SPE(固相萃取)滤筒上,辐照富集水中存在的所有其他阳离子和水溶性放射性核素杂质被收集在废瓶中。下一步是用生理盐水(0.9%NaCl)洗脱筒中的氟离子。本研究旨在确定最适合用于常规生产的阴离子交换固相萃取药筒[18F],并满足欧洲药典各论中氟化钠放射性药物的质量要求。为此,作为开发内部生产方法的一部分,使用四种不同类型的阴离子交换筒进行了手工生产。考察了吸附剂、底物和药筒的反离子对最终收率和所产放射性药物质量的影响。该研究还旨在确定ph参数在限制范围内所需的生理溶液的最小体积。结果表明,不同阴离子交换液的质量参数:外观、化学纯度、放射化学纯度和放射性核素纯度均符合规定的验收标准,使用不同阴离子交换液的质量参数无差异。pH分析表明,滤筒类型和反离子影响[18F]NaF溶液的最终pH值。本研究证实了QMA-Cl-、QMA-CO32-和ps - oh -三种阴离子交换树脂可用于生产。在使用QMA-Cl-的实验中,即使没有稀释,也可以获得所需的pH值。其他墨盒可用于[18F]NaF生产过程,但为了获得验收标准中的pH值,需要进一步稀释。在本研究的基础上,选择QMA-Cl-作为一种药筒,用于进一步开发[18F]NaF放射性药物生产的内部方法。
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RESEARCH ON THE INFLUENCE OF DIFFERENT TYPES OF ANION-EXCHANGE CARTRIDGES ON THE QUALITY OF [18F]NAF RADIOPHARMACEUTICAL AS PART OF PRODUCTION PROCESS DEVELOPMENT
[18F]Sodium Fluoride radiopharmaceutical is a sterile solution for intravenous administration, intendedfor skeletal visualization by positron emission tomography (PET). [18F]Sodium Fluoride for bone imaging wasintroduced in early 1960's, but with the increased availability of PET scanners in the last two decades, thisradiopharmaceutical has growing use in clinical practice for the detection of bone metastases. The productionprocess of [18F]NaF includes production of the radioisotope [18F]F- and purification and formulation of the [18F]NaFradiopharmaceutical. The radioisotope [18F]F- is produced by a cyclotron via the 18O(p,n)18F nuclear reaction,followed by recovery of [18F]F- from [18O] proton-irradiated water by adsorption and desorption from anionexchangeresins. The fluoride anions are trapped on the anion-exchange SPE (solid-phase extraction) cartridge, andall other cationic and water-soluble radionuclide impurities present in irradiated enriched water are collected in thewaste vial. Next step is desorption of the fluoride anions from the cartridge by elution with saline solution (0.9%NaCl). This study aimed to define the most appropriate type of anion-exchange SPE cartridge which could be usedfor routine production [18F]Sodium fluoride radiopharmaceutical which meets the quality requirements defined inEuropean pharmacopeia monograph. For that purpose, as part of development of in-house production method,manual productions with four different types of anion-exchange cartridges were performed. The influence of sorbentsubstrate and counter-ion of the cartridge on the final yield and the quality of the produced radiopharmaceutical wasinvestigated. The study also aimed to define the minimum volume of physiological solution required for the pHparameter to be within limits.The results have shown that the quality parameters: appearance, chemical purity, radiochemical purity andradionuclide purity were in defined acceptance criteria and did not differ when using different anion-exchangecartridges. The pH analyses have demonstrated that the type of cartridge and counter-ion influence the final pH of[18F]NaF solution. This study confirmed that the three types of anion-exchange resins (QMA-Cl-, QMA-CO32- andPS-OH-) could be used for production. In the experiments where QMA-Cl- was used, the required pH level wasobtained even without dilution. The other cartridges could be used in the [18F]NaF production process, but furtherdilution is necessary in order to obtain the pH value in acceptance criteria. On the basis of this study, the QMA-Cl- ischosen as a cartridge to be used in the further development of the in-house method for [18F]NaF radiopharmaceuticalproduction.
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