详细信息
Protonated-chitosan sponge with procoagulation activity for hemostasis in coagulopathy ( SCI-EXPANDED收录)
文献类型:期刊文献
英文题名:Protonated-chitosan sponge with procoagulation activity for hemostasis in coagulopathy
作者:Huang, Zhenhua[1];Zhang, Dong[1];Tong, Laiqiang[1];Gao, Fan[1];Zhang, Shaozan[1];Wang, Xinqing[1];Xie, Yina[1];Chen, Fangping[1,2];Liu, Changsheng[1,2]
机构:[1]East China Univ Sci & Technol, Engn Res Ctr Biomed Mat, Minist Educ, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
年份:2024
卷号:41
起止页码:174
外文期刊名:BIOACTIVE MATERIALS
收录:;WOS:【SCI-EXPANDED(收录号:WOS:001412667800001)】;
基金:This investigation was supported by the National Natural Science Foundation of China (No. 32171342; 51772100), National Key Research and Development Program of China (2022YFB3804300). The authors thank Research Center of Analysis and Test of East China University of Science and Technology for the help on the characterization.
语种:英文
摘要:Hemostatic materials are essential for managing acute bleeding in medical settings. Chitosan (CS) shows promise in hemostasis but its underlying mechanism remains incompletely understood. We unexpectedly discovered that certain protonated-chitosan (PCS) rapidly assembled plasma proteins to form protein membrane (PM) upon contact with platelet-poor plasma (PPP). We hypothesized that the novel observation was intricately related to the procoagulant effect of chitosan. Herein, the study aimed to elucidate the conditions necessary and mechanism for PM formation, identify the proteins within the PM and PCS's procoagulant action at the molecule levels. We confirmed that the amount of -NH3+ groups (>4.9 mmol/g) on PCS molecules played a crucial role in promoting coagulation. The -NH3+ group interacted with blood's multiple active components to exert hemostatic effects: assembling plasma proteins including coagulation factors such as FII, FV, FX, activating blood cells and promoting the secretion of coagulation-related substances (FV, ADP, etc) by platelets. Notably, the hemostatic mechanism can be extended to protonated-chitosan derivatives like quaternized, alkylated, and catechol-chitosan. In the blood clotting index (BCI) experiment, compared to other groups, PCS95 achieved the lowest BCI value (similar to 6 %) within 30 s. Protonated-chitosan exhibited excellent biocompatibility and antibacterial properties, with PCS95 demonstrating inhibition effectiveness of over 95 % against Escherichia coli (E.coil) and Staphylococcus aureus (S. aureus). Moreover, PCS performed enhanced hemostatic effectiveness over chitosan-based commercially agents (Celox (TM) and ChitoGauze (R) XR) in diverse bleeding models. In particular, PCS95 reduced bleeding time by 70 % in rabbit models of coagulopathy. Overall, this study investigated the coagulation mechanism of materials at the molecular level, paving the way for innovative approaches in designing new hemostatic materials.
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