Zhang Chengdong, Fei Yachen, Li Meng, Li Jing, Tang Maomao, Wang Guichun, Li Jiaxin, Wang Yuxiao, Ding Yang, Peng Chengjun, Li Mengjie, Gui Shuangying, Guo Jian
Department of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui 230012, China.
Department of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui 230012, China.
Int J Biol Macromol. 2025 May;307(Pt 4):142080. doi: 10.1016/j.ijbiomac.2025.142080. Epub 2025 Mar 17.
Periodontitis is an oral chronic inflammatory disease induced by pathogenic bacteria. Pathogens continuously activate immune cells to express a large number of pro-inflammatory factors and reactive oxygen species, eventually leading to periodontal tissue damage. Poor eradication of pathogenic bacteria, persistent inflammatory response and impaired periodontal tissue regeneration are the main challenges to control the progression of periodontitis. However, current clinical drug treatment fails to comprehensively address these issues. In this paper, a chitosan-P407-PNIPAM scaffold multi-crosslinked hydrogel (A/CQ-ML@Gel) encapsulating AgNPs and lipid complex (CQ-ML) is developed. This hydrogel shows thermo- and pH-sensitive properties, exhibits excellent injectability, high viscosity and reliable post-injection mechanical strength. A/CQ-ML@Gel possesses a significant antibacterial effect to Porphyromonas gingivalis after implantation, and then by virtue of the programmed release of quercetin microemulsion and caffeic acid phenethyl ester in CQ-ML, exerting excellent inflammation regulation and osteogenic differentiation of periodontal ligament stem cells. Notably, A/CQ-ML@Gel could activate mitophagy through PINK1/Parkin in inflammatory macrophages, thereby inhibiting the production of excess reactive oxygen species, ultimately reprogramming M1/M2 macrophages phenotype for inflammation suppression. In summary, we present an innovative insight into periodontal delivery system for trimodal synergistic therapy strategy in periodontitis.
牙周炎是一种由病原菌引起的口腔慢性炎症性疾病。病原菌持续激活免疫细胞,使其表达大量促炎因子和活性氧,最终导致牙周组织损伤。病原菌清除不佳、持续的炎症反应以及牙周组织再生受损是控制牙周炎进展的主要挑战。然而,目前的临床药物治疗未能全面解决这些问题。在本文中,开发了一种包裹有银纳米颗粒和脂质复合物(CQ-ML)的壳聚糖-P407-聚N-异丙基丙烯酰胺支架多交联水凝胶(A/CQ-ML@Gel)。这种水凝胶具有温度和pH敏感性,表现出优异的可注射性、高粘度和可靠的注射后机械强度。A/CQ-ML@Gel植入后对牙龈卟啉单胞菌具有显著的抗菌作用,然后通过CQ-ML中槲皮素微乳液和咖啡酸苯乙酯的程序性释放,对牙周膜干细胞发挥优异的炎症调节和成骨分化作用。值得注意的是,A/CQ-ML@Gel可通过PINK1/Parkin在炎性巨噬细胞中激活线粒体自噬,从而抑制过量活性氧的产生,最终重编程M1/M2巨噬细胞表型以抑制炎症。综上所述,我们提出了一种针对牙周炎三联协同治疗策略的牙周递送系统的创新见解。