深静脉
医学
血栓形成
药物输送
靶向给药
药品
药理学
血小板
生物医学工程
材料科学
外科
内科学
纳米技术
作者
Hang Xiao,Xiangrui Meng,Songtao Li,Zhiyong Li,Shuo Fang,Yaonan Wang,Jing Li,Jianyuan Tang,Li Ma
出处
期刊:Biomaterials
[Elsevier]
日期:2024-06-17
卷期号:311: 122670-122670
标识
DOI:10.1016/j.biomaterials.2024.122670
摘要
After orthopedic surgeries, such as hip replacement, many patients are prone to developing deep vein thrombosis (DVT), which in severe cases can lead to fatal pulmonary embolism or major bleeding. Clinical intervention with high-dose anticoagulant therapy inevitably carries the risk of bleeding. Therefore, a targeted drug delivery system that adjusts local DVT lesions and potentially reduces drug dosage and toxic side effects important. In this study, we developed a targeted drug delivery platelet-derived nanoplatform (AMSNP@PM-rH/A) for DVT treatment that can simultaneously deliver a direct thrombin inhibitor (DTI) Recombinant Hirudin (rH), and the Factor Xa inhibitor Apixaban (A) by utilizing Aminated mesoporous silica nanoparticles (AMSNP). This formulation exhibits improved biocompatibility and blood half-life and can effectively eliminate deep vein thrombosis lesions and achieve therapeutic effects at half the dosage. Furthermore, we employed various visualization techniques to capture the targeted accumulation and release of a platelet membrane (PM) coating in deep vein thrombosis and explored its potential targeting mechanism.
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