强力霉素
牙周纤维
牙周炎
牙槽
巨噬细胞极化
化学
再生(生物学)
剥皮和根面刨削
自愈水凝胶
生物医学工程
纳米复合材料
药品
牙科
巨噬细胞
抗生素
抗菌活性
药理学
生物相容性
骨愈合
控制释放
M2巨噬细胞
细胞毒性
生物相容性材料
伤口愈合
生物材料
作者
Xiang Yu,Huiling Liu,Leyan Chen,Xiaohui Cheng,Gang Wu,Tymour Forouzanfar,Longbao Feng,Rui Guo,Miao Zhou,Ting Sun
标识
DOI:10.1016/j.bioactmat.2025.09.030
摘要
Periodontitis is a chronic inflammatory disease caused by bacterial infection that leads to the destruction of periodontal tissues. Traditional treatment involves scaling and root planing combined with antibiotics, but systemic antibiotic therapy often results in insufficient drug concentration at the treatment site and unwanted side effects. Here, we developed a nanocomposite thermosensitive hydrogel (CFMD) designed for localized drug delivery. The chitosan-grafted Pluronic® F127 hydrogel (CP) had natural antibacterial activity. After the thermosensitive material flows into the periodontal pocket, it transforms into a gel phase at body temperature, filling the periodontal pocket and preserving the nanomedicine. As the hydrogel retained in the periodontal pocket is degraded, folic acid-modified MBG nanoparticles loaded with doxycycline (FA-MBG@Dox) nanoparticles deliver doxycycline hydrochloride (Dox) to below the gum line, where instruments and hydrogel drug carriers cannot reach, enabling deeper antibacterial, anti-inflammatory, and osteogenesis-promoting effects. In vitro, CFMD hydrogel exhibited potent antibacterial activity, promoted human periodontal ligament stem cells (hPDLSCs) differentiation, and induced macrophage polarization toward the anti-inflammatory (M2) phenotype. In vivo, it effectively inhibited alveolar bone loss, promoted bone regeneration, and reshaped the inflammatory microenvironment. This study showed that CFMD hydrogel with targeted polarization regulation, oxidative stress regulation and osteogenesis regeneration capabilities may provide a simpler and more effective way for the treatment of periodontitis.
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