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Enhanced angiogenesis through controlled release of basic fibroblast growth factor from peptide amphiphile for tissue regeneration

机译:通过控制肽两亲物释放碱性成纤维细胞生长因子来增强血管生成,从而促进组织再生

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In the present study, we hypothesized that a novel approach to promote vascularization would be to create injectable three-dimensional (3-D) scaffolds with encapsulated growth factor that enhance the sustained release of growth factor and induce the angiogenesis. We demonstrate that a 3-D scaffold can be formed by mixing of peptide-amphiphile (PA) aqueous solution with basic fibroblast growth factor (bFGF) suspension. PA was synthesized by standard solid phase chemistry that ends with the alkylation of the NH2 terminus of the peptide. A 3-D network of nanofibers was formed by mixing bFGF suspensions with dilute aqueous solutions of PA. Scanning electron microscopy (SEM) observation revealed the formation of fibrous assemblies with an extremely high aspect ratio and high surface areas. In vitro and in vivo release profile of bFGF from 3-D network of nanofibers was investigated while angiogenesis induced by the released bFGF was assessed. When aqueous solution of PA was subcutaneously injected together with bFGF suspension into the back of mice, a transparent 3-D hydrogel was formed at the injected site and induced significant angiogenesis around the injected site, in marked contrast to bFGF injection alone or PA injection alone. The combination of bFGF-induced angiogenesis is a promising procedure to improve tissue regeneration. (c) 2006 Elsevier Ltd. All rights reserved.
机译:在本研究中,我们假设一种促进血管生成的新方法将是创建具有封装的生长因子的可注射三维(3-D)支架,从而增强生长因子的持续释放并诱导血管生成。我们证明了可以通过将肽-两亲(PA)水溶液与碱性成纤维细胞生长因子(bFGF)悬浮液混合来形成3-D支架。 PA是通过标准固相化学合成的,该化学以肽的NH2末端的烷基化结束。通过将bFGF悬浮液与PA的稀水溶液混合来形成3D纳米纤维网络。扫描电子显微镜(SEM)的观察表明,具有极高的长宽比和高表面积的纤维组件的形成。研究了bFGF从3D纳米纤维网络的体外和体内释放特性,同时评估了由释放的bFGF诱导的血管生成。当将PA水溶液与bFGF悬浮液一起皮下注射到小鼠背部时,在注射部位会形成透明的3-D水凝胶,并在注射部位周围引起明显的血管生成,这与单独bFGF注射或单独PA注射形成鲜明对比。 bFGF诱导的血管生成的组合是改善组织再生的有前途的程序。 (c)2006 Elsevier Ltd.保留所有权利。

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