Multifunctional Metal-Phenolic Composites Promote Efficient Periodontitis Treatment via Antibacterial and Osteogenic Properties.
Hongxiang MeiHai LiuChuanlu ShaQinyi LvQiantao SongLinli JiangErkang TianZiqi GaoJuan LiJiajing ZhouPublished in: ACS applied materials & interfaces (2024)
Periodontitis, a complex inflammatory disease initiated by bacterial infections, presents a significant challenge in public health. The increased levels of reactive oxygen species and the subsequent exaggerated immune response associated with periodontitis often lead to alveolar bone resorption and tooth loss. Herein, we develop multifunctional metal-phenolic composites (i.e., Au@MPN-BMP2) to address the complex nature of periodontitis, where gold nanoparticles (AuNPs) are coated by metal-phenolic networks (MPNs) and bone morphogenetic protein 2 (BMP2). In this design, MPNs exhibit remarkable antibacterial and antioxidant properties, and AuNPs and BMP2 promote osteogenic differentiation of bone marrow mesenchymal stem cells under inflammatory conditions. In a rat model of periodontitis, treatment with Au@MPN-BMP2 leads to notable therapeutic outcomes, including mitigated oxidative stress, reduced progression of inflammation, and the significant prevention of inflammatory bone loss. These results highlight the multifunctionality of Au@MPN-BMP2 nanoparticles as a promising therapeutic approach for periodontitis, addressing both microbial causative factors and an overactivated immune response. We envision that the rational design of metal-phenolic composites will provide versatile nanoplatforms for tissue regeneration and potential clinical applications.
Keyphrases
- oxidative stress
- reduced graphene oxide
- mesenchymal stem cells
- immune response
- gold nanoparticles
- bone loss
- bone regeneration
- public health
- drug delivery
- reactive oxygen species
- dna damage
- stem cells
- diabetic rats
- visible light
- cancer therapy
- microbial community
- induced apoptosis
- metabolic syndrome
- climate change
- anti inflammatory
- type diabetes
- toll like receptor
- dendritic cells
- combination therapy
- risk assessment
- inflammatory response
- signaling pathway
- replacement therapy
- quantum dots
- soft tissue
- essential oil