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A vascular tissue engineering scaffold with core-shell structured nano-fibers formed by coaxial electrospinning and its biocompatibility evaluation

机译:具有同轴电纺丝形成的核壳结构纳米纤维的血管组织工程支架及其生物相容性评价

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摘要

In this article, a tubular vascular tissue engineering scaffold with core-shell structured fibers was produced by coaxial electrospinning at an appropriate flow rate ratio between the inner and outer solution. PCL was selected as the core to provide the mechanical property and integrity to the scaffold while collagen was used as the shell to improve the attachment and proliferation of vascular cells due to its excellent biocompatibility. The fine core-shell structured fibers were demonstrated by scanning electron microscope and transmission electron microscope observations. Subsequently, the collagen shell was crosslinked by genipin and further bound with heparin. The crosslinking process was confirmed by the increasing of tensile strength, swelling ratio and thermogravimetric analysis measurements while the surface heparin content was characterized by means of a UV-spectrophotometer and activated partial thromboplastin time tests. Furthermore, the mechanical properties such as stitch strength and bursting pressure of the as-prepared scaffold were measured. Moreover, the biocompatibility of the scaffold was evaluated by cytotoxicity investigation with L929 cells via MTT assay. Endothelial cell adhesion assessments were conducted to reveal the possibility of the formation of an endothelial cell layer on the scaffold surface, while the ability of smooth muscle cell penetration into the scaffold wall was also assessed by confocal laser scanning microscopy. The as-prepared core-shell structured scaffold showed promising potential for use in vascular tissue engineering.
机译:在本文中,通过在内部溶液和外部溶液之间的适当流速比下进行同轴电纺丝,生产了具有核-壳结构纤维的管状血管组织工程支架。选择PCL作为核心,为支架提供机械性能和完整性,同时由于其出色的生物相容性,将胶原蛋白用作外壳,以改善血管细胞的附着和增殖。通过扫描电子显微镜和透射电子显微镜观察证明了核壳结构细纤维。随后,胶原蛋白壳通过genipin交联并进一步与肝素结合。交联过程通过拉伸强度,溶胀率和热重分析法测量值的增加得到证实,而表面肝素含量通过紫外分光光度计和活化的部分凝血活酶时间测试来表征。此外,测量了所制备的脚手架的机械性能,例如缝合强度和破裂压力。此外,通过MTT测定法对L929细胞进行细胞毒性研究,评价了支架的生物相容性。进行内皮细胞粘附评估以揭示在支架表面上形成内皮细胞层的可能性,同时还通过共聚焦激光扫描显微镜评估了平滑肌细胞渗透到支架壁中的能力。所制备的核-壳结构支架显示出在血管组织工程中使用的有希望的潜力。

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