脚手架
聚己内酯
PLGA公司
生物医学工程
材料科学
药物输送
骨愈合
松质骨
化学
骨形态发生蛋白2
控制释放
复合材料
纳米技术
外科
体外
聚合物
生物化学
纳米颗粒
医学
作者
Yuzhu He,Qindong Wang,Yuqi Liu,Zijiao Zhang,Zheng Cao,Shuo Wang,Ying Xiang,Guowu Ma,Xiumei Wang,Huiying Liu
出处
期刊:Polymers
[MDPI AG]
日期:2024-08-23
卷期号:16 (17): 2394-2394
标识
DOI:10.3390/polym16172394
摘要
Biomaterials play an important role in treating bone defects. The functional characteristics of scaffolds, such as their structure, mechanical strength, and antibacterial and osteogenesis activities, effectively promote bone regeneration. In this study, mineralized collagen and polycaprolactone were used to prepare loaded porous scaffolds with bilayer-structured microspheres with dual antibacterial and osteogenesis functions. The different drug release mechanisms of PLGA and chitosan in PLGA/CS microspheres caused differences in the drug release models in terms of the duration and rate of Pac-525 and BMP-2 release. The prepared PLGA(BMP-2)/CS(Pac-525)@MC/PCL scaffolds were analyzed in terms of physical characteristics, bioactivity, and antibacterial properties. The scaffolds with a dimensional porous structure showed similar porosity and pore diameter to cancellous bone. The release curve of the microspheres and scaffolds with high encapsulation rates displayed the two-stage release of Pac-525 and BMP-2 over 30 days. It was found that the scaffolds could inhibit S. aureus and E. coli and then promote ALP activity. The PLGA(BMP-2)/CS(Pac-525)@MC/PCL scaffold could be used as a dual delivery system to promote bone regeneration.
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