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聚多巴胺和明胶涂层用于快速内皮化血管支架。

Polydopamine and gelatin coating for rapid endothelialization of vascular scaffolds.

机构信息

Warsaw University of Technology, Faculty of Chemical and Process Engineering, Division of Biotechnology and Bioprocess Engineering, BioMedical Engineering Laboratory, Waryńskiego 1, 00-645 Warsaw, Poland.

ENT-Department, Section of Experimental Oncology und Nanomedicine (SEON), Else Kröner-Fresenius-Stiftung-Professorship, Universitätsklinikum Erlangen, Germany.

出版信息

Biomater Adv. 2022 Mar;134:112544. doi: 10.1016/j.msec.2021.112544. Epub 2021 Nov 14.

Abstract

Rapid endothelialization helps overcome the limitations of small-diameter vascular grafts. To develop biomimetic non-thrombogenic coatings supporting endothelialization, medical-grade polyurethane (PU) nanofibrous mats and tubular scaffolds with a diameter below 6 mm prepared by solution blow spinning were coated with polydopamine (PDA), or PDA and gelatin (PDA/Gel). The scaffolds were characterized by scanning electron microscopy, porosity measurement, tensile testing, wettability, Fourier Transform Infrared spectroscopy, and termogravimetric analysis, followed by the measurement of coating stability on the tubular scaffolds. The effect of coating on scaffold endothelialization and hemocompatibility was evaluated using human umbilical vein endothelial cells (HUVECs) and human platelets, showing low numbers of adhering platelets and significantly higher numbers of HUVECs on PDA- and PDA/Gel-coated mats compared to control samples. Tubular PU scaffolds and commercial ePTFE prostheses coated with PDA or PDA/Gel were colonized with HUVECs using radial magnetic cell seeding. PDA/Gel-coated samples achieved full endothelial coverage within 1-3 days post-endothelialization. Altogether, PDA and PDA/Gel coating significantly enhance the endothelialization on the flat surfaces, tubular small-diameter scaffolds, and commercial vascular prostheses. The presented approach constitutes a fast and efficient method of improving scaffold colonization with endothelial cells, expected to work equally well upon implantation.

摘要

快速内皮化有助于克服小直径血管移植物的局限性。为了开发支持内皮化的仿生性非血栓形成涂层,通过溶液吹纺制备的医用级聚氨基甲酸酯(PU)纳米纤维垫和直径低于 6 毫米的管状支架用聚多巴胺(PDA)或 PDA 和明胶(PDA/Gel)进行了涂层。通过扫描电子显微镜、孔隙率测量、拉伸试验、润湿性、傅里叶变换红外光谱和热重分析对支架进行了表征,随后测量了管状支架上涂层的稳定性。通过人脐静脉内皮细胞(HUVEC)和人血小板评估涂层对支架内皮化和血液相容性的影响,结果表明,与对照样品相比,PDA 和 PDA/Gel 涂层的垫子上黏附的血小板数量较少,而 HUVEC 数量明显更多。使用径向磁细胞接种法,将 PDA 或 PDA/Gel 涂层的管状 PU 支架和商业 ePTFE 假体进行了 HUVEC 定植。PDA/Gel 涂层样品在内皮化后 1-3 天内实现了完全内皮覆盖。总之,PDA 和 PDA/Gel 涂层显著增强了平面、小管径支架和商业血管假体上的内皮化。所提出的方法构成了一种快速有效的方法,可改善内皮细胞对支架的定植,预期在植入时同样有效。

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