Department of Periodontology, School and Hospital of Stomatology, Tianjin Medical University, Tianjin 300070, P. R. China.
Department of Polymer Science and Engineering, Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, P. R. China.
ACS Nano. 2024 Oct 29;18(43):29507-29521. doi: 10.1021/acsnano.4c05677. Epub 2024 Oct 14.
Irreversible alveolar bone resorption is one of the important clinical manifestations of periodontitis, which is initiated by a plaque biofilm and exacerbated by the imbalance of osteoclast activity and osteogenesis, affecting a patient's masticatory function and resulting in a high recurrence rate of periodontitis. Herein, to reestablish bone homeostasis in periodontitis, a minocycline hydrochloride (MH)-loaded glycopeptide hydrogel (MH/GRW) is fabricated to mediate alveolar bone absorption through sequential antibacterial and RANKL-blocking activities. GRW shows an ECM-like fibrous and porous microstructure serving as a scaffold for cell proliferation and differentiation and holds the merits including injectability, self-healing properties, and good biocompatibility. After injection in situ, MH is released rapidly from the hydrogel in the early stage, demonstrating a potent antimicrobial effect to combat the biofilm in the deep periodontal pocket. Moreover, MH/GRW exhibits a high specific binding efficiency with RANKL to suppress osteoclast maturation by shielding the RANKL/RANK interaction and enhancing osteogenic differentiation, thereby synergistically regulating bone homeostasis. In the rat periodontitis model, MH/GRW significantly curtails periodontitis progression through antimicrobial activity, inhibition of alveolar bone resorption, and promotion of bone regeneration, which is superior to the treatment of a commercial gel. These findings suggest that MH/GRW with superiority in regulating bone homeostasis provides a promising therapeutic strategy for periodontitis.
不可逆性牙槽骨吸收是牙周炎的重要临床表现之一,由菌斑生物膜引发,并因破骨细胞活性和骨生成失衡而加剧,影响患者的咀嚼功能,导致牙周炎复发率高。在此,为了在牙周炎中重新建立骨稳态,制备了载米诺环素盐酸盐(MH)的糖肽水凝胶(MH/GRW),通过顺序的抗菌和 RANKL 阻断活性来介导牙槽骨吸收。GRW 呈现出类似细胞外基质的纤维状和多孔微观结构,可用作细胞增殖和分化的支架,具有可注射性、自修复特性和良好的生物相容性等优点。原位注射后,MH 在早期从水凝胶中快速释放,表现出强大的抗菌作用,以对抗深部牙周袋中的生物膜。此外,MH/GRW 与 RANKL 具有高特异性结合效率,通过屏蔽 RANKL/RANK 相互作用和增强成骨分化来抑制破骨细胞成熟,从而协同调节骨稳态。在大鼠牙周炎模型中,MH/GRW 通过抗菌活性、抑制牙槽骨吸收和促进骨再生显著抑制牙周炎进展,优于商业凝胶的治疗效果。这些发现表明,具有调节骨稳态优势的 MH/GRW 为牙周炎提供了一种有前景的治疗策略。