Department of Radio-pharmacology, Institut Curie Site Saint-Cloud, Saint-Cloud, France.
Nuclear Medicine, Hôpital Tenon, Paris, France.
J Labelled Comp Radiopharm. 2021 Sep;64(11):440-446. doi: 10.1002/jlcr.3938. Epub 2021 Aug 14.
Radiolabelling with short half-lives radionuclides (e.g., fluorine-18 and carbon-11) must be as efficient and as fast as possible. Nucleophilic radiofluorinations and radiomethylations are conducted in polar aprotic solvents, such as dimethylsulfoxyde (DMSO), N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA), at high temperature. Those solvents are classified as toxic according to the ICH guidelines and must be evaluated in drug such as radiopharmaceuticals. Headspace gas chromatography is the standard method for the quantification of residual solvents but is not optimized for a rapid quantification of low vapor pressure solvents such as DMSO, DMF and DMA in radiopharmaceuticals. Direct injection gas chromatography is an interesting option without incubation step but the analysis run-time remains beyond 10 min long. In consequence, we developed a very simple ultra-high performance liquid chromatography method coupled with UV detection. Following the EMA requirements, we successfully validated a 3-min run-time analysis for quantification of three solvents in short half-lives radiopharmaceuticals. We currently use this method for the quality control of radiopharmaceuticals produced in our PET center.
使用半衰期较短的放射性核素(例如氟-18 和碳-11)进行放射性标记,必须尽可能高效和快速。亲核放射性氟化和放射性甲基化在极性非质子溶剂中进行,例如二甲亚砜(DMSO)、N,N-二甲基甲酰胺(DMF)和 N,N-二甲基乙酰胺(DMA),在高温下进行。根据 ICH 指南,这些溶剂被归类为有毒物质,必须在药物(如放射性药物)中进行评估。顶空气相色谱法是残留溶剂定量的标准方法,但不适用于快速定量放射性药物中低蒸气压溶剂(如 DMSO、DMF 和 DMA)。直接进样气相色谱法是一种无需孵育步骤的有趣选择,但分析运行时间仍超过 10 分钟。因此,我们开发了一种非常简单的超高效液相色谱法,结合紫外检测。根据 EMA 的要求,我们成功验证了一种 3 分钟运行时间的分析方法,用于定量测定半衰期较短的放射性药物中的三种溶剂。我们目前将该方法用于我们的 PET 中心生产的放射性药物的质量控制。