聚己内酯
材料科学
生物医学工程
涂层
组织工程
静电纺丝
明胶
血栓形成
韧性
复合材料
血管
肝素
聚合物
聚乙烯醇
生物材料
抗凝剂
模数
聚酯纤维
表面改性
血细胞
延伸率
弹性模量
作者
Lin Jiang,Meirong Su,Ziying Guo,Yue Zhang,Lijuan Zheng,Chengyong Wang
标识
DOI:10.1021/acsapm.5c04728
摘要
The development of small-diameter artificial blood vessels for the treatment of cardiovascular disease faces critical challenges, including mismatches in mechanical properties, poor cellular compatibility, and a high propensity for thrombosis. In this study, we fabricated polycaprolactone (PCL)-based small-diameter vascular scaffolds by melt electrospinning technology. By optimizing processing parameters, we successfully constructed a vascular framework with a hierarchical fibrous network. Biomimetic vascular scaffolds with three distinct architectures (star, triangle, and square) were systematically compared in terms of their performance. Further surface multifunctionalization was achieved using NaOH-induced hydrophilization, Ethyldimethylaminopropyl carbodiimide/N-hydroxy succinimide (EDC/NHS)-mediated heparin grafting, and coating with a rutin-loaded gelatin methacryloyl (GelMA) hydrogel. Analysis demonstrated that the optimized structure of stars met the mechanical requirements of human coronary arteries, exhibiting a fracture elongation of 929.8% and a Young’s modulus exceeding 1.5 MPa. The 0.1% rutin-loaded coating enabled sustained drug release with <6% mass loss over 6 days while maintaining high cell viability. Furthermore, heparinization significantly enhanced anticoagulant properties, with hemolysis rates <5%. Overall, we present an integrated “process-structure-function” strategy to successfully engineer small-diameter artificial blood vessels with favorable mechanical performance, biocompatibility, and in vitro anticoagulant properties, thereby providing a reliable material platform and technical route for the in-depth fundamental research and further developmental exploration of small-diameter vascular substitutes.
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