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经生物活性涂层改性的血管型聚氨酯假体:物理化学、力学和生物学性能。

Vascular Polyurethane Prostheses Modified with a Bioactive Coating-Physicochemical, Mechanical and Biological Properties.

机构信息

Biomedical Engineering Laboratory, Faculty of Chemical and Process Engineering, Warsaw University of Technology, Warynskiego 1, 00-645 Warsaw, Poland.

出版信息

Int J Mol Sci. 2021 Nov 10;22(22):12183. doi: 10.3390/ijms222212183.

Abstract

This study describes a method for the modification of polyurethane small-diameter (5 mm) vascular prostheses obtained with the phase inversion method. The modification process involves two steps: the introduction of a linker (acrylic acid) and a peptide (REDV and YIGSR). FTIR and XPS analysis confirmed the process of chemical modification. The obtained prostheses had a porosity of approx. 60%, Young's Modulus in the range of 9-11 MPa, and a water contact angle around 40°. Endothelial (EC) and smooth muscle (SMC) cell co-culture showed that the surfaces modified with peptides increase the adhesion of ECs. At the same time, SMCs adhesion was low both on unmodified and peptide-modified surfaces. Analysis of blood-materials interaction showed high hemocompatibility of obtained materials. The whole blood clotting time assay showed differences in the amount of free hemoglobin present in blood contacted with different materials. It can be concluded that the peptide coating increased the hemocompatibility of the surface by increasing ECs adhesion and, at the same time, decreasing platelet adhesion. When comparing both types of peptide coatings, more promising results were obtained for the surfaces coated with the YISGR than REDV-coated prostheses.

摘要

本研究描述了一种用于修饰相转化法获得的小直径(5 毫米)聚氨酯血管移植物的方法。修饰过程包括两个步骤:引入连接剂(丙烯酸)和肽(REDV 和 YIGSR)。FTIR 和 XPS 分析证实了化学修饰过程。所得到的移植物具有约 60%的孔隙率、9-11 MPa 的杨氏模量和约 40°的水接触角。内皮(EC)和平滑肌(SMC)细胞共培养表明,用肽修饰的表面增加了 EC 的黏附性。同时,SMC 在未修饰和肽修饰的表面上的黏附性均较低。血液材料相互作用分析表明,所获得的材料具有高血液相容性。全血凝固时间测定表明,与不同材料接触的血液中游离血红蛋白的含量存在差异。可以得出结论,肽涂层通过增加 ECs 的黏附性,同时减少血小板黏附性,提高了表面的血液相容性。在比较两种类型的肽涂层时,YISGR 涂层的表面比 REDV 涂层的移植物具有更有前景的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86c9/8623365/cb64ef01dc14/ijms-22-12183-g001.jpg

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