体内
纳米团簇
离体
清道夫受体
模态(人机交互)
可视化
医学
化学
癌症研究
材料科学
纳米技术
生物
内科学
计算机科学
胆固醇
数据挖掘
脂蛋白
人机交互
生物技术
作者
Jiahui Wang,Menglin Wu,Jin Chang,Liang Li,Qi Guo,Jianwen Hao,Qizhen Peng,Baoshuai Zhang,Xuening Zhang,Xue Li
标识
DOI:10.1016/j.nano.2019.04.003
摘要
Owing to the high morbidity and mortality of cardiovascular diseases resulting from atherosclerosis, developing specific noninvasive diagnostic methods to distinguish vulnerable atherosclerotic plaques becomes urgent and mandatory. Herein, scavenger receptors AI (SR-AI), a secreted biomarker associated with foam macrophages, was selected as a target for identifying vulnerable plaques. A dual-modality imaging probe (PP1-Au@GSH@Gd NCs) was constructed by covalently attaching a peptidic SR-AI ligand, PP1 to gadolinium-integrated gold nanoclusters, which exhibited remarkably improved fluorescence signal and longitudinal relaxivity with highly loaded Au and Gd species. In vitro cellular binding studies showed preferential affinity of PP1-Au@GSH@Gd NCs to activated macrophages in SR-AI-dependent manner. In vivo MR/fluorescence images presented robust and prolonged plaque contrast enhancement in established ApoE-/- mice models thanks to favorable targeting efficacy of PP1-Au@GSH@Gd NCs. Collectively, the noninvasive MR/fluorescence molecular imaging strategy with PP1-Au@GSH@Gd NCs holds great promise for precise clinical diagnosis of vulnerable plaques.
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