Chitosan-vancomycin hydrogel incorporated bone repair scaffold based on staggered orthogonal structure: a viable dually controlled drug delivery system

脚手架 聚乳酸 生物相容性 壳聚糖 复合数 药物输送 材料科学 生物医学工程 化学 复合材料 纳米技术 生物化学 医学 聚合物 冶金
作者
Xiaohan Gao,Zexian Xu,Shangbo Li,Lidi Cheng,Dian Xu,Li Li,Liqiang Chen,Yaoxiang Xu,Zijian Liu,Yanshan Liu,Jian Sun
出处
期刊:RSC Advances [The Royal Society of Chemistry]
卷期号:13 (6): 3759-3765 被引量:20
标识
DOI:10.1039/d2ra07828g
摘要

In clinical practice, challenges remain in the treatment of large infected bone defects. Bone tissue engineering scaffolds with good mechanical properties and antibiotic-controlled release are powerful strategies for infection treatment. In this study, we prepared polylactic acid (PLA)/nano-hydroxyapatite (nHA) scaffolds with vertical orthogonal and staggered orthogonal structures by applying 3D printing technology. In addition, vancomycin (Van)-based chitosan (CS) hydrogel (Gel@Van) was loaded on the scaffold (PLA/nHA/CS-Van) to form a local antibiotic release system. The microstructure of the composite scaffold had high porosity with interconnected three-dimensional networks. The mechanical properties of the PLA/nHA/CS-Van composite scaffold were enhanced by the addition of CS-Van. The results of the water contact angle analysis showed that the hydrophilicity of the drug-loaded scaffold improved. In addition, the composite scaffold could produce sustained release in vitro for more than 8 weeks without adverse effects on the proliferation and differentiation of mouse embryonic osteoblasts (MC3T3-E1), which confirmed its good biocompatibility. During the in vitro antimicrobial study, the composite scaffold effectively inhibited the growth of Staphylococcus aureus (S. aureus). Therefore, our results suggest that the PLA/nHA/CS-Van composite scaffold is a promising strategy for treating infected bone defects.
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