钆
体内
化学
转基因小鼠
离体
共轭体系
磁共振成像
分子成像
淀粉样蛋白(真菌学)
荧光
阿尔茨海默病
临床前影像学
生物物理学
核磁共振
转基因
病理
医学
体外
生物化学
疾病
生物
无机化学
有机化学
生物技术
量子力学
放射科
聚合物
物理
基因
作者
Garam Choi,Hee-Kyung Kim,Ahrum Baek,Soyeon Kim,Min Jung Kim,Minsup Kim,Art E. Cho,Gang Ho Lee,Hoesu Jung,Ji-ung Yang,Taekwan Lee,Yongmin Chang
标识
DOI:10.1016/j.jiec.2019.11.031
摘要
Multifunctional imaging of the deposition of amyloid-beta (Aβ) aggregates in the brain is of great importance in diagnosing Alzheimer’s disease. Herein, we report a multifunctional Aβ-targeting small-molecular-weight gadolinium (Gd)-based contrast agent (CA), Gd-DO3A-Chal (a new Gd-chelate conjugated with chalcone), that showed 8 times higher binding affinity to Aβ aggregates than a previously reported Gd-chelate conjugated with Pittsburgh compound B. Gd-DO3A-Chal showed multimodal imaging capability. As a new fluorescence imaging probe, Gd-DO3A-Chal showed a good match with immunostained images using 6E10 monoclonal antibodies for the detection of Aβ aggregates in 5XFAD transgenic mouse brain sections. For in vivo magnetic resonance (MR) imaging without blood-brain barrier disruption, longitudinal relaxation time (T1)-weighted MR images after intravenous administration of Gd-DO3A-Chal showed signal enhancement of the Aβ distribution in living 5XFAD transgenic mouse brain. Therefore, in vivo MR images for Aβ detection in addition to fluorescent optical images of Aβ aggregates with high specificity and sensitivity using this new multifunctional Aβ-targeting CA were successfully demonstrated.
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