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将 REDV 方便地掺入多孔丝素纤维支架中,以增强厚组织的血管生成。

Facile incorporation of REDV into porous silk fibroin scaffolds for enhancing vascularization of thick tissues.

机构信息

Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, School of Biological Science and Medical Engineering, Beihang University, Beijing 100083, People's Republic of China; School of Life Information Science and Instrument Engineering, Hangzhou Dianzi University, Hangzhou 310018, Zhejiang Province, People's Republic of China.

Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, School of Biological Science and Medical Engineering, Beihang University, Beijing 100083, People's Republic of China.

出版信息

Mater Sci Eng C Mater Biol Appl. 2018 Dec 1;93:96-105. doi: 10.1016/j.msec.2018.07.062. Epub 2018 Jul 25.

Abstract

Rapid neovascularization within scaffolds is critical for the regeneration of thick complex tissues. The surface immobilization of peptides and other active molecules have been explored to improve the vascularization capacity of implants. However, the rapid degradation of these molecules, the reaction conditions and cross-linking usually result in decreased vascularization capability. Here, we introduced a temperate, all-aqueous process to achieve bulk porous silk fibroin (SF) scaffolds. A temperature controlled process was used to induce the water stable structure by SF self-assembly. Arg-Glu-Asp-Val (REDV) peptides were added into SF solution and fixed within SF scaffolds during the self-assembly process. The results showed that the functionalized scaffolds markedly promoted the adhesion of endothelial cells in vitro. Moreover, the in vivo studies indicated enhanced cell infiltration in the bulk functionalized SF scaffolds and impressive vascularization at 4 weeks post-implantation. The functionalized scaffolds demonstrated excellent vascularization capability, providing an exciting biomaterial option for thick tissue regeneration.

摘要

快速的支架内新血管生成对于厚复杂组织的再生至关重要。已经探索了肽和其他活性分子的表面固定化以提高植入物的血管生成能力。然而,这些分子的快速降解、反应条件和交联通常会导致血管生成能力下降。在这里,我们引入了一种温和的全水相工艺来实现块状多孔丝素(SF)支架。通过 SF 自组装来控制温度诱导水稳定结构。将 Arg-Glu-Asp-Val (REDV) 肽添加到 SF 溶液中,并在自组装过程中将其固定在 SF 支架内。结果表明,功能化支架显著促进了体外内皮细胞的黏附。此外,体内研究表明,在植入后 4 周时,大块功能化 SF 支架中的细胞浸润得到增强,血管生成效果显著。功能化支架表现出优异的血管生成能力,为厚组织再生提供了一种令人兴奋的生物材料选择。

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