细菌纤维素
螯合作用
化学
脐静脉
纤维素
凝血时间
核化学
内生
基质(化学分析)
表面改性
金属
血小板
抗凝剂
凝血酶
羧甲基纤维素
生物医学工程
材料科学
生物物理学
化学工程
凝结
心脏瓣膜
机械心脏
铜
作者
Penghao Song,Yuping Shu,Shaoqiang Ling,Xianzu Ling,Yi-Xiang Wang,Zhiwei Yang,Yizao Wan,Quanchao Zhang
摘要
ABSTRACT Bacterial cellulose (BC) is a promising polymeric nanofibrous matrix material for heart valve prostheses. However, its endothelialization and anticoagulation properties remain suboptimal. To overcome these limitations, herein, Cu 2+ @BC composites (Cu 2+ @BC‐1~4) were fabricated by immobilizing Cu 2+ on BC surfaces via polydopamine (PDA) self‐polymerization and metal ion chelation. Results showed that immobilized Cu 2+ on BC could stably catalyze sustained NO release from endogenous donors, with Cu 2+ @BC‐3 maintaining NO release within a physiological range for up to 70 days. In the presence of endogenous NO donors, all Cu 2+ @BC samples exhibited significantly improved anticoagulation, including reduced hemolysis, decreased platelet adhesion, and prolonged clotting times. Moreover, NO release remarkably promoted the adhesion, proliferation, and migration of human umbilical vein endothelial cells (HUVECs), with Cu 2+ @BC‐3 showing the optimal endothelialization effect. This study demonstrates that Cu 2+ chelation modification endows BC with excellent anticoagulant and endothelialization properties, making Cu 2+ @BC a potential candidate matrix material for heart valve replacement.
科研通智能强力驱动
Strongly Powered by AbleSci AI