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Synthesis and Characterization of Degradable Polar Hydrophobic ionic Polyurethane Scaffolds for Vascular Tissue Engineering Applications

机译:血管组织工程应用中可降解极性疏水离子型聚氨酯支架的合成与表征

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摘要

In tissue engineering, the ability to manipulate scaffold design characteristics is important to achieve functional tissue regeneration. In this study, degradable polar hydrophobic ionic polyurethane (D-PHI) porous scaffolds were synthesized using a lysine-based divinyl oligomer (DVO). Optimization studies on the DVO and D-PHI scaffold synthesis were conducted to maximize is'ocyanate and methacrylate monomer conversion, respectively. D-PHI scaffold properties were manipulated through the introduction of a lysine-based cross-linker. Specifically, increasing D-PHI cross-linker concentration resulted in an increase of the elastic modulus (0.5-21 MPa), a decrease of the elongation-at-yield (45-5%) and a reduction of scaffold swelling (170-100%). Based on a preliminary study with A10 vascular smooth muscle cells, D-PHI scaffolds demonstrated the ability to support cell adhesion and growth during 2 weeks of culture, suggesting their potential suitability for longer term vascular tissue engineering. The versatility of the D-PHI properties may allow for the tailoring of cell-material interaction and ultimately functional tissue regeneration.
机译:在组织工程中,操纵支架设计特征的能力对于实现功能性组织再生很重要。在这项研究中,使用基于赖氨酸的二乙烯基低聚物(DVO)合成了可降解的极性疏水离子聚氨酯(D-PHI)多孔支架。进行了DVO和D-PHI支架合成的优化研究,以分别最大化异氰酸酯和甲基丙烯酸酯的单体转化率。通过引入基于赖氨酸的交联剂来操纵D-PHI支架的性质。具体而言,增加D-PHI交联剂的浓度会导致弹性模量(0.5-21 MPa)的增加,屈服伸长率的降低(45-5%)和支架膨胀的降低(170-100) %)。基于对A10血管平滑肌细胞的初步研究,D-PHI支架展示了在培养2周内支持细胞黏附和生长的能力,表明它们对长期血管组织工程的潜在适用性。 D-PHI特性的多功能性可允许定制细胞-材料相互作用并最终实现功能性组织再生。

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