牙周炎
炎症
牙槽
下调和上调
促炎细胞因子
抗生素
药理学
医学
化学
炎症反应
癌症研究
细胞
骨形成
大鼠模型
巨噬细胞
牙科
生物安全
转染
细胞存活
间充质干细胞
作者
Qiurui Hu,Yonghui Huang,Hao Liang,Xianxian Huang,X B Li,Le Chen,Lingling Liang,Qinglan Lu,Guangqi Zhou,Xiaoping Su,Cuiping Li,X B Li,Xinglu Jiang
标识
DOI:10.1021/acsbiomaterials.5c01515
摘要
compared to EGCG-Zn alone. Meanwhile, EGCG-Zn@FG was also shown to have anti-inflammatory effects by reducing the expression of inflammatory factors (IL-1β and IL-6). It is worth mentioning that EGCG-Zn@FG was also verified to upregulate the expression of osteogenic factors (Col-1, ALP, and Runx-2) through the release of EGCG, promoting alveolar bone repair. In rat models, EGCG-Zn@FG in the treatment area was slowly and continuously released for 24 h after administration. Notably, the administration of EGCG-Zn@FG not only exhibited remarkable capability in mitigating dental inflammation and facilitating bone repair, but also ensured favorable biosafety in periodontitis rat models, thereby highlighting its dual advantages in therapeutic efficacy and biocompatibility. Collectively, these findings validate EGCG-Zn@FG as a promising antibiotic-alternative strategy to address antibiotic resistance in periodontitis while possessing substantial potential for clinical treatment of periodontal disease.
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