GMP compliant simplified fast and high yielding automated synthesis of [18F]fallypride without the need of HPLC purification

IF 4.4 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Ammar Alfteimi, Yi Zhao, Ulf Lützen, Alexander Helm, Michael Jüptner, Maaz Zuhayra
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引用次数: 0

Abstract

Background

[18F]Fallypride PET has been used to study D2/3 receptor occupancy and density in neuropsychiatric disorders including Huntington’s disease (HD) and aging in humans. Nevertheless, the various synthetic methods including those provided by commercial synthesizers for [18F]fallypride exhibit a disadvantage concerning the necessity of using a HPLC purification step, which causes difficulties in the automation, leads to long synthesis times and moderate yields. Therefore utilizing the purification step by SPE cartridges is considered highly desirable for future commercialization of radiopharmaceutical cassettes. In our lab we have developed a simplified reliable automatic Radiosynthesis of [18F]fallypride by using SPE cartridges for the purification step without the need of HPLC.

Results

A simplified Radiosynthesis of [18F]fallypride has been developed without the use of HPLC for both a commercial cassette based synthesis system (AllinOne (AiO) system, Trasis, Belgium) and a research synthesis module with fixed tubing (RNplus, Synthra, Germany). The cleaning step involves a serial combination of several SPE cartridges. The synthesis time was shortened by 44% compared to synthesis using HPLC. At the same time the not decay corrected yield increases from 44 to 59% by using TBAHCO3 as phase transfer catalysts and from 17 to 31% for the synthesis with K2CO3/Kryptofix-[2.2.2] compared to synthesis using HPLC. The Radiochemical purity was always > 98% and all quality control parameters (e.g. sterility, endotoxin, stability and Radiochemical purity) conformed with requirements of the European Pharmacopoeia.

Conclusions

A GMP compliant automatic synthesis of [18F]fallypride including purification using simple solid phase extraction cartridges instead of HPLC was developed and evaluated. The implementation of the simplified synthesis in both used commercial modules allows efficient and reproducible Radiosynthesis of [18F]fallypride and leads to short synthesis times and high radiochemical yields with high radiochemical purity.

符合GMP要求,简化了快速高效的自动合成[18F],无需HPLC纯化
[18F]Fallypride PET已被用于研究人类亨廷顿病(HD)等神经精神疾病和衰老中D2/3受体的占用和密度。然而,包括商业合成器为[18F]fallypride提供的合成方法在内的各种合成方法都存在一个缺点,即必须使用HPLC纯化步骤,这导致自动化困难,合成时间长,收率中等。因此,利用SPE墨盒的纯化步骤被认为是未来放射性药物盒商业化的高度可取的。在我们的实验室中,我们开发了一种简化的可靠的自动放射性合成[18F]fallypride,使用SPE滤池进行纯化步骤,而不需要HPLC。结果针对商用盒式合成系统(AllinOne (AiO)系统,Trasis,比利时)和研究用固定管合成模块(RNplus, Synthra,德国),开发了一种无需高效液相色谱的简化放射性合成[18F] falypride。清洗步骤涉及几个SPE墨盒的串行组合。与HPLC法相比,合成时间缩短了44%。与此同时,与HPLC合成相比,使用TBAHCO3作为相转移催化剂,未衰减校正的产率从44%提高到59%,使用K2CO3/Kryptofix-[2.2.2]合成的产率从17%提高到31%。放射化学纯度始终为98%,所有质量控制参数(如无菌性、内毒素、稳定性和放射化学纯度)符合欧洲药典的要求。结论建立了一种符合GMP要求的自动合成[18F]黄酮的方法,采用简单固相萃取筒代替高效液相色谱进行纯化。在使用的两种商业模块中实现简化的合成,可以实现[18F]fallypride的高效和可重复的放射性合成,并导致合成时间短,具有高放射化学纯度的高放射化学产率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
8.70%
发文量
30
审稿时长
5 weeks
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