牙周炎
再生(生物学)
壳聚糖
牙槽
炎症
富血小板纤维蛋白
化学
药理学
间充质干细胞
吸收
活性氧
体内
血小板源性生长因子受体
生长因子
生物医学工程
细胞生物学
纤维蛋白
牙科
医学
生物化学
免疫学
病理
生物
生物技术
受体
作者
Jinmin Zhou,Houxuan Li,Shuhong Li,Yuhan Wang,He Wang,Jie Li,Yiyao Hu,Jinlin Song,Jichun Yang,Yang Luo
标识
DOI:10.1021/acsbiomaterials.4c01784
摘要
Diabetes exacerbates periodontitis by overexpressing reactive oxygen species (ROS), which leads to periodontal bone resorption. Consequently, it is imperative to relieve inflammation and promote alveolar bone regeneration comprehensively for the development of diabetic periodontal treatment strategies. Furthermore, an orderly treatment to avoid interference between these two processes can achieve the optimal therapeutic effect. Thus, we constructed a sequential sustained release system based on the zeolitic imidazolate framework-8 (ZIF-8)-modified chitosan thermosensitive hydrogel (TOOTH) for diabetic periodontal therapy in this work. Chemically modified tetracycline-3 (CMT-3) and platelet-derived growth factor-BB (PDGF-BB) were loaded in the hydrogel and ZIF-8 for sequential release, respectively, with the aim of reducing inflammation and facilitating tissue regeneration. During the therapy, CMT-3 first escaped from the hydrogel due to degradation and diffusion for ROS elimination. Subsequently, ZIF-8 was dissociated under an acid microenvironment, and PDGF-BB was sustainably released to promote osteogenesis. The release intervals between CMT-3 and PDGF-BB could be regulated by the sizes of ZIF-8. The biocompatible TOOTH exhibited a favorable therapeutic effect for diabetic periodontitis in vitro and in vivo. The sequentially controlled release of CMT-3 and PDGF-BB facilitated by TOOTH holds promise for promoting periodontal tissue regeneration and offers potential for clinical translation.
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