化学
正电子发射断层摄影术
阿片受体
体内
Pet成像
类阿片
药代动力学
分子成像
药理学
放射合成
临床前影像学
神经影像学
受体
放射化学
核医学
生物化学
神经科学
医学
心理学
生物技术
生物
作者
So Jeong Lee,Torben D. Pearson,Maëva Dhaynaut,Alexander C. MacDonagh,Hsiao‐Ying Wey,Moses Q. Wilks,Bryan L. Roth,Jacob M. Hooker,Marc D. Normandin
标识
DOI:10.1021/acs.jmedchem.4c02287
摘要
Carfentanil, a highly potent synthetic opioid, paradoxically serves as a crucial positron emission tomography (PET) imaging tool in neurobiological studies of the mu-opioid receptor (MOR) system when labeled with carbon-11 ([11C]CFN). However, its clinical research use is hindered by extreme potency and the limited availability of short-lived carbon-11 (t1/2 = 20.4 min). We present fluorine-18-labeled fluorocarfentanils ([18F]FCFNs), which can be produced at higher molar activity, allowing for lower mass doses and benefiting from the longer half-life of fluorine-18 (t1/2 = 109.8 min), facilitating broader accessibility. Using copper-mediated radiofluorination, we synthesized a small [18F]FCFN library and conducted preclinical imaging evaluations. Two candidates, o-18F-1 and p-18F-2, showed optimal brain uptake, favorable pharmacokinetics, and high MOR-specific binding. Selectivity was confirmed through in vitro binding assays and in vivo PET scans. These [18F]FCFNs are promising for accessible human brain MOR imaging.
科研通智能强力驱动
Strongly Powered by AbleSci AI