Fluorine-18-Labeled Diaryl-azines as Improved ?-Amyloid Imaging Tracers: From Bench to First-in-Human Studies

被引:15
|
作者
Li, Yuying [1 ]
Zhou, Kaixiang [2 ]
Zhang, Xiaojun [3 ]
Zhao, Hailong [4 ]
Wang, Xiaoming [4 ]
Dong, Ruilin [4 ]
Wang, Yan [5 ]
Chen, Baian [6 ,7 ]
Yan, Xiao-xin [5 ]
Dai, Jiapei [8 ]
Sui, Yanying [4 ]
Zhang, Jinming [3 ]
Cui, Mengchao [1 ,2 ]
机构
[1] Beijing Normal Univ, Key Lab Radiopharmaceut, Minist Educ, Beijing 100875, Peoples R China
[2] Beijing Normal Univ Zhuhai, Ctr Adv Mat Res, Zhuhai 519087, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Nucl Med, Beijing 100853, Peoples R China
[4] HighTech Atom Co Ltd, Beijing 102413, Peoples R China
[5] Cent South Univ, Xiangya Sch Med, Dept Anat & Neurobiol, Changsha 410013, Peoples R China
[6] Capital Med Univ, Sch Basic Med Sci, Beijing Key Lab Neural Regenerat & Repair, Beijing 100069, Peoples R China
[7] Capital Med Univ, Sch Basic Med Sci, Dept Lab Anim Sci, Beijing 100069, Peoples R China
[8] South Cent Univ Nationalities, Wuhan Inst Neurosci & Neuroengn, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
ALZHEIMERS-DISEASE; PET AGENTS; BETA; PLAQUES; PROBES; F-18-AZD4694; DERIVATIVES; TARGET; BRAIN;
D O I
10.1021/acs.jmedchem.2c01503
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The deposition of fi-amyloid (Afi) in the brain is a pathologic hallmark of Alzheimer's disease (AD), appearing years before the onset of symptoms, and its detection is incorporated into clinical diagnosis. Here, we have discovered and developed a class of diaryl-azine derivatives for detecting Afi plaques in the AD brain using PET imaging. After a set of comprehensive preclinical assessments, we screened out a promising Afi-PET tracer, [18F]92, with a high binding affinity to the Afi aggregates, significant binding ability with the AD brain sections, and optimal brain pharmacokinetic properties in rodents and non-human primates. The first -inhuman PET study declared that [18F]92 displayed low white matter uptake and could bind to Afi pathology for distinguishing AD from healthy control subjects. All these results support that [18F]92 might become a promising PET tracer for visualizing Afi pathology in AD patients.
引用
收藏
页码:4603 / 4616
页数:14
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