止血
伤口愈合
纤维蛋白
血小板
化学
凝结
止血剂
纳米纤维
肽
凝血酶
药理学
医学
生物化学
免疫学
外科
纳米技术
材料科学
内科学
作者
Huange Xu,Qi-Lin Liang,Litao Li,Gao-Feng Qi,Lei Wang,Li-Ning Zhan,Meng-Ru Ding,Kuo Zhang,Xu Cui
出处
期刊:Biomaterials Science
[The Royal Society of Chemistry]
日期:2022-01-01
卷期号:10 (10): 2628-2637
被引量:4
摘要
Uncontrolled hemorrhage is a major problem both in surgical intervention and after trauma. Herein, we design an in situ constructable peptide network, mimicking and participating in the native coagulation process for enhanced hemostasis and wound healing. The network consists of two peptides including C6KL, mimicking platelets and C6KG, mimicking fibrin. The C6KL nanoparticles could bind to the collagen at the wound site and transform into C6KL nanofibers. The C6KG nanoparticles could bind to GPIIb/IIIa receptors on the surface of activated platelets and transform into C6KG nanofibers. The in situ formed peptide network could interwind platelets, fibrin and red blood cells, causing embolism at the wound site. In a lethal femoral artery, vein, and nerve cut model of rats, the amount of bleeding was reduced to 32.8% by C6KL and C6KG with chitosan/alginate. The biomimetic peptides show great clinical potential as trauma hemostatic agents.
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