血管组织工程用高分子支架的研制

E. Velikanova, V. Matveeva, E. Krivkina, V. Sevostianova, M. Khanova, T. V. Glushkova, Y. Kudryavtseva, L. Antonova
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引用次数: 0

摘要

组织工程的一个重要领域是开发小直径血管移植物。在我们的研究中,我们评估了电纺丝聚合物支架是否有利于组织工程移植的发展。聚合物移植物由聚羟基丁酸酯/戊酸酯和聚己内酯(PHBV/PCL)的混合物和加入I型胶原制成。此外,用纤维连接蛋白处理移植物。从冠状动脉疾病(CAD)患者的外周血中分离细胞,然后将其植入移植物腔面。然后,在脉动流生物反应器中培养带细胞的移植物。我们证实,在静电纺丝过程中,PHBV/PCL和I型胶原蛋白的分离喂养可以为血管移植物提供适合维持管腔表面内皮层活力的支架。组织工程的一个重要领域是开发小直径血管移植物。在我们的研究中,我们评估了电纺丝聚合物支架是否有利于组织工程移植的发展。聚合物移植物由聚羟基丁酸酯/戊酸酯和聚己内酯(PHBV/PCL)的混合物和加入I型胶原制成。此外,用纤维连接蛋白处理移植物。从冠状动脉疾病(CAD)患者的外周血中分离细胞,然后将其植入移植物腔面。然后,在脉动流生物反应器中培养带细胞的移植物。我们证实,在静电纺丝过程中,PHBV/PCL和I型胶原蛋白的分离喂养可以为血管移植物提供适合维持管腔表面内皮层活力的支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a polymeric scaffold for vascular tissue engineering
An important area of tissue engineering is the development of small-dimeter vascular grafts. In our study we assessed whether an electrospun polymer scaffold is beneficial for developing a tissue-engineered graft. The polymeric grafts were made from a blend of polyhydroxybutyrate/valerate and polycaprolactone (PHBV/PCL) and added type I collagen. Additionally, the grafts were treated with fibronectin. Cells were isolated from the peripheral blood of patients with coronary artery disease (CAD) and then seeded on the luminal graft surface. Then, the grafts with cells were cultured in a pulsatile flow bioreactor. We confirmed that separate feeding of PHBV/PCL and type I collagen during electrospinning allows developing a scaffold for a vascular graft suitable for maintaining the viability of the endothelial layer on the luminal surface.An important area of tissue engineering is the development of small-dimeter vascular grafts. In our study we assessed whether an electrospun polymer scaffold is beneficial for developing a tissue-engineered graft. The polymeric grafts were made from a blend of polyhydroxybutyrate/valerate and polycaprolactone (PHBV/PCL) and added type I collagen. Additionally, the grafts were treated with fibronectin. Cells were isolated from the peripheral blood of patients with coronary artery disease (CAD) and then seeded on the luminal graft surface. Then, the grafts with cells were cultured in a pulsatile flow bioreactor. We confirmed that separate feeding of PHBV/PCL and type I collagen during electrospinning allows developing a scaffold for a vascular graft suitable for maintaining the viability of the endothelial layer on the luminal surface.
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