血栓
血栓形成
溶栓
血小板
材料科学
生物医学工程
医学
静脉血栓形成
药物输送
尿激酶
心脏病学
内科学
纳米技术
心肌梗塞
作者
Junhui Zhang,Fan Hu,Junzhe Zhang,Jing Xie,Li Wang,Linwen Lv,Haojun Liang,Qiuyang Liu,Ranran Chen,Hao Li,Wenxi Su,Ruyu Yan,Ziteng Chen,Li Wang,Hongyu Tang,Yanan Chang,Juan Li,Hao Chen,Shen Ming-hua,Gengmei Xing,Kui Chen
出处
期刊:Small
[Wiley]
日期:2024-10-21
标识
DOI:10.1002/smll.202406262
摘要
Abstract The heterogeneity of thrombi in terms of composition, structure, and blood rheology parameters presents a challenge for effective thrombus‐targeting drug delivery. To address this, a self‐adaptive nano‐delivery system, termed D‐PLT, is developed. It consists of platelet membrane‐cloaked deformable mesoporous organic silicon dioxide nanocomposite, enabling it to respond to the challenge of the heterogeneity of thrombi in arteries and veins. The system exhibits progressive targeting, with the ability to target arterial and venous thrombosis and damaged blood vessels. D‐PLT physically matches the pore structure of the thrombus by undergoing varied deformation, leading to advanced targeting and enrichment of arterial and venous thrombus. When co‐loaded with the thrombolytic drug urokinase (UK) and the endothelium‐protecting agent atorvastatin calcium (AT), the system improves rapid vascular opening of arterial and venous thrombosis in 90 min and provides up to 7 days of durable thrombolysis and recovery from endothelial dysfunction in vivo. This self‐adaptive delivery system offers a promising strategy to overcome thrombus heterogeneity.
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