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锌激活动态水凝胶通过增强血管生成与骨生成的耦合来加速骨再生。

Zinc-energized dynamic hydrogel accelerates bone regeneration via potentiating the coupling of angiogenesis and osteogenesis.

作者信息

Lv Nanning, Zhou Zhangzhe, Hong Lihui, Li Hongye, Liu Mingming, Qian Zhonglai

机构信息

Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, China.

Department of Orthopedic Surgery, The Affiliated Lianyungang Clinical College of Xuzhou Medical University (The Second People's Hospital of Lianyungang), Lianyungang, China.

出版信息

Front Bioeng Biotechnol. 2024 Apr 3;12:1389397. doi: 10.3389/fbioe.2024.1389397. eCollection 2024.

Abstract

Insufficient initial vascularization plays a pivotal role in the ineffectiveness of bone biomaterials for treating bone defects. Consequently, enhancing the angiogenic properties of bone repair biomaterials holds immense importance in augmenting the efficacy of bone regeneration. In this context, we have successfully engineered a composite hydrogel capable of promoting vascularization in the process of bone regeneration. To achieve this, the researchers first prepared an aminated bioactive glass containing zinc ions (AZnBg), and hyaluronic acid contains aldehyde groups (HA-CHO). The composite hydrogel was formed by combining AZnBg with gelatin methacryloyl (GelMA) and HA-CHO through Schiff base bonding. This composite hydrogel has good biocompatibility. In addition, the composite hydrogel exhibited significant osteoinductive activity, promoting the activity of ALP, the formation of calcium nodules, and the expression of osteogenic genes. Notably, the hydrogel also promoted umbilical vein endothelial cell migration as well as tube formation by releasing zinc ions. The results of study demonstrated that implantation of the composite hydrogel in the bone defect of the distal femur of rats could effectively stimulate bone generation and the development of new blood vessels, thus accelerating the bone healing process. In conclusion, the combining zinc-containing bioactive glass with hydrogels can effectively promote bone growth and angiogenesis, making it a viable option for the repair of critical-sized bone defects.

摘要

初始血管化不足在骨生物材料治疗骨缺损无效中起关键作用。因此,增强骨修复生物材料的血管生成特性对于提高骨再生疗效至关重要。在此背景下,我们成功设计了一种能够在骨再生过程中促进血管化的复合水凝胶。为此,研究人员首先制备了含锌离子的胺化生物活性玻璃(AZnBg)和含醛基的透明质酸(HA-CHO)。通过席夫碱键合将AZnBg与甲基丙烯酰化明胶(GelMA)和HA-CHO结合形成复合水凝胶。这种复合水凝胶具有良好的生物相容性。此外,复合水凝胶表现出显著的骨诱导活性,促进碱性磷酸酶(ALP)活性、钙结节形成和成骨基因表达。值得注意的是,该水凝胶还通过释放锌离子促进脐静脉内皮细胞迁移和管腔形成。研究结果表明,将复合水凝胶植入大鼠股骨远端骨缺损处可有效刺激骨生成和新血管发育,从而加速骨愈合过程。总之,含锌生物活性玻璃与水凝胶结合可有效促进骨生长和血管生成,使其成为修复临界尺寸骨缺损的可行选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b9e/11022217/e96e72a9f2bd/fbioe-12-1389397-g001.jpg

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