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首页> 外文期刊>Journal of biomedical materials research, Part A >Heparin-lmmobilized Biodegradable Scaffolds For Local and Sustained Release of Angiogenic Growth Factor
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Heparin-lmmobilized Biodegradable Scaffolds For Local and Sustained Release of Angiogenic Growth Factor

机译:肝素固定的可生物降解支架用于血管生成生长因子的局部和持续释放。

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Heparin-immobilized porous biodegradable scaffolds were fabricated to release basic fibroblast growth factor (bFGF) in a sustained manner. Heparin was covalently conjugated onto the surface of macroporous PLGA scaffolds fabricated by a gas-foaming/salt-leaching method. Sustained release of bFGF was successfully achieved for over 20 days due to high affinity of bFGF onto the immobilized heparin. It appears that bFGF release rate was regulated by the specific interaction between bFGF and heparin. The bFGF fraction released from the scaffolds maintained its bioactivity, as judged from determining the proliferation extent of human umbilical vein endothelial cells (HUVECs) in vitro. When heparin-immobilized scaffolds loaded with bFGF were implanted subcutaneously in vivo, they effectively induced the formation of blood vessels in the vicinity of the implant site. This study demonstrated that local and sustained delivery of angiogenic growth factor for tissue regeneration could be achieved by surface modification of porous scaffolds with heparin
机译:制备固定有肝素的多孔可生物降解支架,以持续释放碱性成纤维细胞生长因子(bFGF)。将肝素共价结合到通过气体发泡/盐浸法制备的大孔PLGA支架的表面上。由于bFGF对固定化肝素的高度亲和力,成功地实现了超过20天的bFGF持续释放。似乎bFGF释放速率受bFGF与肝素之间的特异性相互作用所调节。从确定体外人脐静脉内皮细胞(HUVECs)的增殖程度判断,从支架释放的bFGF组分保持其生物活性。当将负载有bFGF的肝素固定支架植入体内皮下植入时,它们有效地诱导了植入部位附近血管的形成。这项研究表明,通过肝素对多孔支架进行表面修饰,可以实现局部和持续递送血管生成生长因子以促进组织再生。

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