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利用丝素蛋白-骨微球复合物重建兔眼眶缺损。

Reconstruction of an orbital defect in rabbits using a silk fibroin-bone microparticle complex.

机构信息

Department of Ophthalmology, Shanghai Xin Shi Jie Eye Hospital, Shanghai, China.

Department of Otology and Skull Base Surgery, Eye and ENT Hospital of Shanghai Medical School, Fudan University, Shanghai, China.

出版信息

Int J Artif Organs. 2022 Oct;45(10):849-856. doi: 10.1177/03913988221113354. Epub 2022 Jul 25.

DOI:10.1177/03913988221113354
PMID:35876430
Abstract

OBJECTIVE

To construct a silk fibroin-bone microparticle composite based on a porous silk fibroin membrane and to study its feasibility as a material to reconstruct an orbital bone defect.

METHODS

A 3D porous silk fibroin membrane scaffold was constructed with a defined pore size and incorporated with bone microparticles from a New Zealand rabbit orbital bone defect. The silk fibroin-bone microparticle composite was then implanted into the orbital bone defect to promote osteogenesis along the surface of the porous silk fibroin membrane. The feasibility of constructing an ideal orbital defect repair material and the silk fibroin-bone micronucleus complex was evaluated by animal experiments, molecular biology, histomorphology, imaging, raw molecular mechanisms, and the biological behavior of the material in vivo.

RESULTS

The silk fibroin-bone microparticle composite promotes angiogenesis and osteogenesis to repair bone defects in vivo. Moreover, SF (silk fibroin)/BD (bone dust) complex promotes osteogenesis and angiogenesis by activating FGF2 (Fibroblast Growth Factor 2) and SF scaffolds can bind and restore FGF2.

CONCLUSION

Silk fibroin is biocompatible and the silk fibroin-bone microparticle complex successfully repaired orbital bone defects. Additionally, fibroblast growth factor expression around or within the remaining incompletely degraded silk fibroin materials was observed in vivo.

摘要

目的

构建基于多孔丝素膜的丝素蛋白-骨微粒复合材料,并研究其作为重建眼眶骨缺损材料的可行性。

方法

采用具有一定孔径的 3D 多孔丝素膜支架,与新西兰兔眼眶骨缺损的骨微粒结合。然后将丝素蛋白-骨微粒复合材料植入眼眶骨缺损部位,以促进多孔丝素膜表面的成骨作用。通过动物实验、分子生物学、组织形态学、影像学等方法,从材料的体内原始分子机制和生物行为等方面,评价构建理想的眼眶缺损修复材料和丝素蛋白-骨微核复合物的可行性。

结果

丝素蛋白-骨微粒复合材料可促进体内血管生成和骨生成,修复骨缺损。此外,SF(丝素蛋白)/BD(骨屑)复合物通过激活 FGF2(成纤维细胞生长因子 2)促进成骨和血管生成,SF 支架可以结合和恢复 FGF2。

结论

丝素蛋白具有良好的生物相容性,丝素蛋白-骨微粒复合材料成功修复了眼眶骨缺损。此外,体内观察到纤维母细胞生长因子在剩余未完全降解的丝素蛋白材料周围或内部的表达。

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