生物相容性
纳米医学
化学
细菌纤维素
骨髓炎
Wnt信号通路
药品
药物输送
炎症
再生(生物学)
痤疮丙酸杆菌
金黄色葡萄球菌
药理学
纳米技术
信号转导
生物相容性材料
枯草芽孢杆菌
巨噬细胞
辛伐他汀
脚手架
作者
Y Han,Yao Zhao,C R Yang,Miao Niu,Jun Dai,Quanxin Ning,Kai Xiao,J-J Liang,Wensheng Zhang,Liang Wang,Dan Shao,Dongsong Li
摘要
Bacterial osteomyelitis remains a formidable challenge in clinic because existing monotherapies fail to block inevitable infection, uncontrolled inflammation, and impaired bone regeneration concurrently. Here, we present an AI-assisted strategy that integrates antibacterial, anti-inflammatory, and pro-osteogenic activities into a single nanocrystal. Through machine learning‑assisted screening from FDA-approved active pharmaceutical ingredients (API), we identified glycyrrhizic acid and simvastatin as a multifunctional combination capable of self-assembling into uniform nanocrystals (SGNCs) with ultrahigh drug loading. SGNCs effectively neutralize reactive oxygen species, suppress M1 macrophage polarization, promote bactericidal effects, and reverse infection-impaired osteogenic differentiation. Mechanistically, RNA sequencing analysis further reveals that the beneficial effects of SGNCs are associated with the inhibition of inflammatory response via cytokine-cytokine receptor interaction pathway and the activation of bone regeneration program via the Wnt signaling pathway. As a consequence, SGNCs eradicate bacterial burden and restore bone microarchitecture with excellent biocompatibility in a rat osteomyelitis model. Our insights highlight an AI-assisted strategy that creates a mechanism-targeting nanomedicine solely from APIs for the efficient treatment of bacterial osteomyelitis, which currently requires multimodal management.
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