去细胞化
细胞外基质
血管内皮生长因子
生物医学工程
聚己内酯
主动脉
生物相容性
材料科学
组织工程
化学
医学
外科
血管内皮生长因子受体
癌症研究
聚合物
生物化学
复合材料
冶金
作者
John Patrick Cuenca,Hoe-Jin Kang,Md. Abdullah Al Fahad,Myeongki Park,Minji Choi,Hyun-Yong Lee,Byong‐Taek Lee
标识
DOI:10.1080/09205063.2022.2069398
摘要
AbstractAbstractAlthough the continuous development of small-diameter vascular grafts (SDVGs) (D < 5 mm) continues, most vascular grafts are made from synthetic polymers, which lead to serious complications from arteriosclerosis, thrombosis, and vascular ischemia. Here, to address these shortcomings, we combine synthetic polymers with natural decellularized small-diameter vessels and loaded with growth factor. We fabricated vascular grafts by electrospinning polycaprolactone (PCL) to decellularized rat aorta matrix (ECM) followed by heparin and vascular endothelial growth factor (VEGF) loading. In- vitro studies showed that PCL/ECM/VEGF vascular grafts, showed excellent hemocompatibility and biocompatibility properties. The vascular grafts implanted into the rat aorta revealed that the PCL/ECM/VEGF grafts promotes endothelial cells and smooth-muscle cells infiltration with a rate of FLK-1, ICAM1, and a-SMA distribution higher than that of the PCL and PCL/ECM vascular grafts at 2 weeks and 4 weeks after implantation. The PCL/ECM/VEGF vascular graft should be considered for potential small-diameter vascular grafts in clinical fields.Keywords: polycaprolactonedecellularized rat aorta matrixvascular endothelial growth factorElectrospinningDecellularizationSmall-diameter vascular grafts Disclosure statementNo potential conflict of interest was reported by the authors.Additional informationFundingWe received the following financial support for the research, authorship, and/or publication of this article. It was supported by a grant (2015R1A6A1A03032522) of the Basic Science Research Program through the National Research Foundation (NRF) funded by the Ministry of Education. It was also partially supported by Soonchunhyang University, South Korea.
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