荧光
原位
巨噬细胞
聚集诱导发射
小泡
生物物理学
荧光寿命成像显微镜
化学
纳米技术
材料科学
生物
生物化学
光学
膜
体外
物理
有机化学
作者
Zhiheng Luo,Xipeng Li,Caifa You,Laiping Fang,Delong Yang,Yunxia Wu,Zhijin Fan,Qin Zeng,Xu Chen,Hua Ma,Junhui Zhao,Shuo Sang,Hongju Yang,Dong Wang,Judun Zheng,Yuhui Liao
出处
期刊:Small methods
[Wiley]
日期:2025-06-02
卷期号:: e2500486-e2500486
被引量:1
标识
DOI:10.1002/smtd.202500486
摘要
Abstract Precise diagnosis of atherosclerosis (AS) is a crucial strategy for reducing acute cardiovascular events. Herein, a macrophage membrane (MM)‐camouflaged biomimetic vesicle loaded with near‐infrared‐II (NIR‐II) aggregation‐induced emission luminogens (AIEgens) (P4TT@MM) is proposed to achieve localized in vivo imaging of atherosclerosis. The AIEgens characteristics of P4TT@MM effectively compensate for the fluorescence intensity decrease caused by the intramolecular torsional charge transfer (TICT) effect, even in foam cell‐rich lesions. Benefiting from the biomimetic camouflage of MM and its strong affinity for atherosclerotic plaques, P4TT@MM enables precise targeting of lesion sites, successfully achieving high‐contrast imaging of atherosclerotic plaques in the carotid arteries and aortas of the AS mice model. Compared with free P4TT, the NIR‐II fluorescence intensity of P4TT@MM is increased by 140% in carotid arteries and 152% in aortas, respectively. Moreover, the P4TT@MM demonstrates robust biocompatibility combined with significant clinical translation potential. This study may present a promising tool for the clinical diagnosis of AS.
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