An improved radiosynthesis of [18F]FAraG, a PET radiotracer for imaging T-cell activation

IF 0.9 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of labelled compounds & radiopharmaceuticals Pub Date : 2022-08-24 DOI:10.1002/jlcr.3999
Daniel P. Holt, Robert F. Dannals
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Abstract

In this concise practitioner protocol, the radiochemical synthesis of 2′-deoxy-2′-[18F]fluoro-9-β-d-arabinofuranosylguanine ([18F]FAraG) suitable for human positron emission tomography (PET) studies is described and the results from validation productions are presented. The high specific activity (sometimes referred to as molar activity) radiotracer product is prepared as a sterile, apyrogenic solution that conforms to current Good Manufacturing Practice (cGMP) requirements established by the U.S. Food and Drug Administration.

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一种用于成像t细胞激活的PET放射性示踪剂[18F]FAraG的改进放射合成
在这个简明的医生方案中,描述了适合人类正电子发射断层扫描(PET)研究的2 ' -脱氧-2 ' -[18F]氟-9-β-d-阿拉伯糖基铀基鸟嘌呤([18F]FAraG)的放射化学合成,并介绍了验证产品的结果。高比活性(有时称为摩尔活性)放射性示踪剂产品制备为无菌无致孕溶液,符合美国食品药品监督管理局制定的现行良好生产规范(cGMP)要求。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
57
审稿时长
1 months
期刊介绍: The Journal of Labelled Compounds and Radiopharmaceuticals publishes all aspects of research dealing with labeled compound preparation and applications of these compounds. This includes tracer methods used in medical, pharmacological, biological, biochemical and chemical research in vitro and in vivo. The Journal of Labelled Compounds and Radiopharmaceuticals devotes particular attention to biomedical research, diagnostic and therapeutic applications of radiopharmaceuticals, covering all stages of development from basic metabolic research and technological development to preclinical and clinical studies based on physically and chemically well characterized molecular structures, coordination compounds and nano-particles.
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