PLGA公司
生物医学工程
骨愈合
再生(生物学)
伤口愈合
体内
材料科学
肽
生物材料
壳聚糖
体外
生物物理学
化学
细胞生物学
纳米技术
生物化学
医学
免疫学
外科
生物
生物技术
作者
Shendan Xu,Guangjie Tian,Min Zhi,Zihao Liu,Yaqi Du,Xuemei Lu,Minting Li,Jin Bai,Xuewen Li,Jiayin Deng,Shiqing Ma,Yonglan Wang
标识
DOI:10.1021/acsbiomaterials.3c01858
摘要
The challenges in the treatment of extensive bone defects are infection control and bone regeneration. Bone tissue engineering is currently one of the most promising strategies. In this study, a short biopeptide with specific osteogenic ability is designed by fusion peptide technology and encapsulated with chitosan-modified poly(lactic acid–glycolic acid) (PLGA) microspheres. The fusion peptide (FP) mainly consists of an osteogenic functional sequence (P-15) and a bone-specific binding sequence (Asp-6), which can regulate bone formation accurately and efficiently. Chitosan-modified PLGA with antimicrobial and pro-healing effects is used to achieve the sustained release of fusion peptides. In the early stage, the antimicrobial and soft tissue healing effects can stop the wound infection as soon as possible, which is relevant for the subsequent bone regeneration process. Our data show that CS-PLGA@FP microspheres have antibacterial and pro-cell migration effects in vitro and excellent pro-wound-healing effects in vivo. In addition, CS-PLGA@FP microspheres promote the expression of osteogenic-related factors and show excellent bone regeneration in a rat defect model. Therefore, CS-PLGA@FP microspheres are an efficient biomaterial that can accelerate the recovery of bone defects.
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