骨感染
骨髓炎
材料科学
药物输送
生物医学工程
金黄色葡萄球菌
连接器
纳米技术
细菌
医学
外科
生物
计算机科学
遗传学
操作系统
作者
Guanghua Lu,Gang Zhao,Shen Wang,Hanqing Li,Qiang Yu,Qi Sun,Bo Wang,Wei Li,Zi Fu,Zhenyu Zhao,Linshan Yang,Lianfu Deng,Xianyou Zheng,Ming Cai,Min Lu
标识
DOI:10.1002/advs.202306964
摘要
Abstract The effective management of osteomyelitis remains extremely challenging due to the difficulty associated with treating bone defects, the high probability of recurrence, the requirement of secondary surgery or multiple surgeries, and the difficulty in eradicating infections caused by methicillin‐resistant Staphylococcus aureus (MRSA). Hence, smart biodegradable biomaterials that provide effective and precise local anti‐infection effects and can promote the repair of bone defects are actively being developed. Here, a novel nano‐micro composite is fabricated by combining calcium phosphate (CaP) nanosheets with drug‐loaded GelMA microspheres via microfluidic technology. The microspheres are covalently linked with vancomycin (Van) through an oligonucleotide (oligo) linker using an EDC/NHS carboxyl activator. Accordingly, a smart nano‐micro composite called “CaP@MS‐Oligo‐Van” is synthesized. The porous CaP@MS‐Oligo‐Van composites can target and capture bacteria. They can also release Van in response to the presence of bacterial micrococcal nuclease and Ca 2+ , exerting additional antibacterial effects and inhibiting the inflammatory response. Finally, the released CaP nanosheets can promote bone tissue repair. Overall, the findings show that a rapid, targeted drug release system based on CaP@MS‐Oligo‐Van can effectively target bone tissue infections. Hence, this agent holds potential in the clinical treatment of osteomyelitis caused by MRSA.
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