Biomaterials · 2025
A triple-responsive nanozyme platform of AgAu-CeO2 heterojunction integrated with probiotics for precision antibacterial therapy in periodontitis.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Li Meiqi, Ding Qihang, Hu Songtao, Qi Manlin, Sun Jiao, Shi Yujia, Dong Biao, Qian Kun, Sun Xiaolin, Cheng Zhen, Wang Lin
Аннотация
Nanozymes hold significant promise for biomedical applications; however, their clinical translation is hindered by the mismatch between physiological conditions and their optimal catalytic environments, particularly with respect to temperature and pH. To address this challenge, we developed a multifunctional composite nanozyme (AgAu C-L, formed by covalent conjugation of AgAu@CeO2 with Lactobacillus reuteri) by anchoring an ultrasmall cerium dioxide (CeO2) nanozyme with peroxidase (POD)-like activity onto silver-gold nanocages (AgAu NCs), and integrating it with Lactobacillus reuteri (L. reuteri). Upon near-infrared light irradiation, the localized surface plasmon resonance effect of AgAu NCs induced dual regulatory mechanisms: photothermal heating, which elevated local temperature to enhance catalytic efficiency, and interfacial electron transfer, which promoted Ce3+/Ce4+ redox cycling to sustain catalytic activity. Simultaneously, L. reuteri modulated the local pH through the secretion of lactic and acetic acids, creating a favorable acidic microenvironment for enzyme function. This triple-modulation strategy markedly enhanced the POD-like activity of CeO2, triggering a robust reactive oxygen species burst that effectively disrupted periodontal biofilms and eliminated pathogenic bacteria. Furthermore, the composite interfered with microbial metabolic pathways, reducing biofilm formation and virulence. Our findings establish a powerful nanozyme-based platform for periodontitis treatment and provide a broadly applicable strategy for optimizing nanozyme performance in vivo.