溶栓药
葡萄激酶
血栓
血小板
药理学
瑞替普酶
链激酶
血栓形成
阿司匹林
尿激酶
替卡格雷
止血
医学
体内
溶栓
重组DNA
内科学
化学
生物
氯吡格雷
心肌梗塞
生物技术
生物化学
基因
作者
Rui Hua,Mingxi Li,Qingxia Lin,Mengying Dong,Xiaoxuan Gong,Zhenyu Lin,Yule Li,Chen Li,Tian Wu,Chunyue Tan,Wenhao Zhang,Qian Wang,Tianyu Wu,Zhou Xiao-yu,Fang Yang,Chunjian Li
标识
DOI:10.1021/acsami.3c18402
摘要
Thrombolytic therapy is one of the most effective treatments for thrombus dissolution and recanalization of blocked vessels in thrombotic diseases. However, the application of the thrombolytic strategy has been limited due to unsatisfactory thrombolytic efficacy, relatively higher bleeding complications, and consequently restricted indications. Recombinant staphylokinase (r-SAK) is a third-generation thrombolytic agent produced by genetic engineering technology, which exhibits a better thrombolytic efficacy than urokinase and recombinant streptokinase. Inspired by the natural affinity of platelets in hemostasis and pathological thrombosis, we developed a platelet membrane (PM)-coated r-SAK (PM-r-SAK). Results from animal experiments and human in vitro studies showed that the PM-r-SAK had a thrombolytic efficacy equal to or better than its 4-fold dose of r-SAK. In a totally occluded rabbit femoral artery thrombosis model, the PM-r-SAK significantly shortened the initial recanalization time compared to the same dose and 4-fold dose of r-SAK. Regarding the recanalized vessels, the PM-r-SAK prolonged the time of reperfusion compared to the same dose and 4-fold dose of r-SAK, though the differences were not significant. An in vitro thrombolytic experiment demonstrated that the thrombolytic efficacy of PM-r-SAK could be inhibited by platelet-poor plasma from patients taking aspirin and ticagrelor. PM coating significantly improves the thrombolytic efficacy of r-SAK, which is related to the thrombus-targeting activity of the PM-r-SAK and can be inhibited by aspirin- and ticagrelor-treated plasma.
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