Su Chengjun, Zhu Mengyao, Guo Yiman, Sun Jiachen, Liu Miao, Ma Yansong, Xu Yan, Bai Yuxing, Che Xiaoxia, Zhang Ning
Department of Orthodontics, School of Stomatology, Capital Medical University, Beijing, 100070, China.
CAS Key Lab of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Mater Today Bio. 2025 Jun 9;33:101969. doi: 10.1016/j.mtbio.2025.101969. eCollection 2025 Aug.
During orthodontic treatment, poor oral hygiene often facilitates the proliferation of cariogenic bacteria, particularly , leading to lactic acid accumulation and subsequent enamel demineralization. To mitigate this issue, Dimethylaminohexadecyl methacrylate (DMAHDM) was incorporated onto the protein-repellent surface of 2-Methacryloyloxyethyl phosphorylcholine (MPC), resulting in the formation of a DMAHDM@MPC composite. This composite was then integrated into resin-modified glass ionomer cement (RMGIC) to develop an antimicrobial orthodontic adhesive, termed RMGIC + MPC + DMAHDM (RMD). This study demonstrated that DMAHDM@MPC nanoparticles self-assembled into a core-shell structure, thereby enhancing the antimicrobial activity. A six-month randomized controlled trial (RCT) involving 29 orthodontic patients, along with metagenomic and metabolomic analyses, revealed that RMD significantly reduced plaque accumulation by selectively inhibiting pathogenic bacteria while preserving beneficial microbiota. Additionally, MPC was shown to competitively bind to sucrose-6-phosphatase (SPP) in pathogenic bacteria, inhibiting sucrose synthesis and carbohydrate metabolism, thus reducing the production of organic acids. In conclusion, RMD effectively prevents enamel demineralization by selectively targeting cariogenic bacteria and their associated sugar metabolism pathways during orthodontic treatment.
在正畸治疗期间,口腔卫生不良常常会促进致龋菌的增殖,尤其是 ,导致乳酸积累以及随后的牙釉质脱矿。为缓解这一问题,将甲基丙烯酸二甲氨基十六烷基酯(DMAHDM)掺入2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)的蛋白质排斥表面,从而形成DMAHDM@MPC复合材料。然后将该复合材料整合到树脂改性玻璃离子水门汀(RMGIC)中,以开发一种抗菌正畸粘合剂,称为RMGIC + MPC + DMAHDM(RMD)。本研究表明,DMAHDM@MPC纳米颗粒自组装成核壳结构,从而增强了抗菌活性。一项涉及29名正畸患者的为期六个月的随机对照试验(RCT)以及宏基因组学和代谢组学分析表明,RMD通过选择性抑制病原菌同时保留有益微生物群,显著减少了牙菌斑的积累。此外,MPC被证明能与病原菌中的蔗糖-6-磷酸酶(SPP)竞争性结合,抑制蔗糖合成和碳水化合物代谢,从而减少有机酸的产生。总之,RMD通过在正畸治疗期间选择性靶向致龋菌及其相关的糖代谢途径,有效预防牙釉质脱矿。