Pharmacokinetic Characterization of [18F]UCB-H PET Radiopharmaceutical in the Rat Brain

被引:27
作者
Becker, Guillaume [1 ]
Warnier, Corentin [1 ]
Serrano, Maria Elisa [1 ]
Bahri, Mohamed Ali [1 ]
Mercier, Joel [2 ]
Lemaire, Christian [1 ]
Salmon, Eric [1 ]
Luxen, Andre [1 ]
Plenevaux, Alain [1 ]
机构
[1] Univ Liege, GIGA Cyclotron Res Ctr In Vivo Imaging, B-4000 Liege, Belgium
[2] UCB BioPharma, B-1420 Braine Lalleud, Belgium
关键词
SV2A; F-18]UCB-H; PET; chirality; population-based input function; SYNAPTIC VESICLE PROTEIN; NEUROTRANSMITTER RELEASE; RADIATION-DOSIMETRY; SV2A RADIOTRACER; INPUT FUNCTION; BINDING-SITE; 2A SV2A; LEVETIRACETAM; EXPRESSION; TRACER;
D O I
10.1021/acs.molpharmaceut.7b00235
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The synaptic vesicle glycoprotein 2A (SV2A), a protein essential to the proper nervous system function, is found in presynaptic vesicles. Thus, SV2A targeting, using dedicated radiotracers combined with positron emission tomography (PET), allows the assessment of synaptic density in the living brain. The first-in-class fluorinated SV2A specific radioligand, [F-18]UCB-H, is now available at high activity through an efficient radiosynthesis compliant with current good manufacturing practices (cGMP). We report here a noninvasive method to quantify [F-18]UCB-H binding in rat brain with microPET. Validation study in rats confirmed the need of high enantiomeric purity to target SV2A in vivo. We demonstrated the reliability of a population-based' input function to quantify SV2A in preclinical microPET Setting. Finally, we investigated the in vivo metabolism of [F-18]UCB-H and confirmed the negligible amount of radiothetabolites in the rat brain. Hence; the in vivo quantification of SV2A using [F-15]UCB-H microPET seems a promising tool for the assessment of the synaptic density in the rat brain, and opens neurodegenerative disease rodent models. the way for longitudinal follow-up in neurodegenerative disease rodent models.
引用
收藏
页码:2719 / 2725
页数:7
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