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胶原/肝素双亲和性多层修饰胶原支架用于控制 bFGF 释放以促进体内血管生成。

Collagen/Heparin Bi-Affinity Multilayer Modified Collagen Scaffolds for Controlled bFGF Release to Improve Angiogenesis In Vivo.

机构信息

Key Laboratory for Nano-Bio Interface Research, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, 215123, P.R. China.

Xi'an Jiaotong University, Xi'an, 710049, P.R. China.

出版信息

Macromol Biosci. 2018 Nov;18(11):e1800086. doi: 10.1002/mabi.201800086. Epub 2018 Aug 29.

Abstract

Basic fibroblast growth factor (bFGF) is an important protein for wound healing and angiogenesis in tissue engineering, but the lack of a viable delivery system hampers its clinical application. This study aims to maintain the long-term controlled release of bFGF by utilizing a collagen/heparin bi-affinity multilayer delivery system (CHBMDS), which is fabricated by the alternate deposition of negatively charged heparin, positively charged collagen, and CBD-bFGF (a collagen-binding domain [CBD] was fused into the native bFGF) via specific or electrostatic interaction. The results show that CHBMDS not only support localized and prolonged release of CBD-bFGF(over 35 days) but also lead to enhanced angiogenesis (higher density and larger diameter (≈70 µm) of newly formed blood vessels in subcutaneous tissue of SD rat after 5 weeks). This system could act as a versatile approach for bFGF delivery and further improve therapeutic efficacy for injured tissues.

摘要

碱性成纤维细胞生长因子(bFGF)是组织工程中伤口愈合和血管生成的重要蛋白,但缺乏可行的递送系统限制了其临床应用。本研究旨在通过利用胶原/肝素双亲和多层递药系统(CHBMDS)来维持 bFGF 的长期控释,该系统是通过带负电荷的肝素、带正电荷的胶原蛋白和 CBD-bFGF(将胶原结合结构域 [CBD] 融合到天然 bFGF 中)之间的特异性或静电相互作用,通过交替沉积制备而成。结果表明,CHBMDS 不仅支持 CBD-bFGF 的局部和长时间释放(超过 35 天),而且还导致血管生成增强(在 5 周后 SD 大鼠皮下组织中,新形成的血管密度更高,直径更大(≈70 µm))。该系统可作为 bFGF 递送的一种多功能方法,进一步提高受损组织的治疗效果。

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