Li Xiaoye, Li Qiang, He Ao, Dang Meng, Zhang Yu, Wang Minjin, Sun Qinhong, Dai Zhuo, Ding Meng, Zheng Jingben, Mou Yongbin, Xiu Weijun, Dong Heng
Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Institute of Stomatology, Nanjing University, 30 Zhongyang Road, Nanjing 210008, China.
Department of Thoracic Surgery, Jiangsu Key Laboratory of Molecular and Translational Cancer Research, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & Nanjing Medical University Affiliated Cancer Hospital, Nanjing 210009, China.
ACS Nano. 2025 Aug 12;19(31):28624-28643. doi: 10.1021/acsnano.5c08035. Epub 2025 Jul 31.
Bacterial infections caused by drug-resistant bacteria persist due to biofilm-mediated tolerance, which limits the efficacy of both antimicrobial agents and host immune defenses. Here, we develop ionic microbubbles (MB-CuTA) self-assembled by FeO@CuTA nanoparticles to enhance copper ion-mediated antibiofilm therapy. Upon ultrasound activation, MB-CuTA undergoes inertial cavitation, disrupting biofilm integrity and generating a localized surge of copper ions. This process achieves a dual therapeutic effect: (1) disruption of bacterial metabolic homeostasis, thereby overcoming the intrinsic resistance of biofilms to conventional antimicrobial agents, and (2) activation of cellular immunity to effectively counteract bacterial immune evasion mechanisms. By breaking biofilm tolerance through both metabolic and immunological pathways, our strategy enables deep copper ion penetration in biofilms and effective infection clearance in both mouse implant infection and peritonitis infection models. Our approach introduces a biofilm tolerance disruption method through inducing bacterial cuproptosis-like death and cellular immunity activation, offering a promising strategy against biofilm infections.
由耐药细菌引起的细菌感染因生物膜介导的耐受性而持续存在,这限制了抗菌药物和宿主免疫防御的功效。在此,我们开发了由FeO@CuTA纳米颗粒自组装而成的离子微泡(MB-CuTA),以增强铜离子介导的抗生物膜治疗。在超声激活后,MB-CuTA发生惯性空化,破坏生物膜完整性并产生局部铜离子激增。这一过程实现了双重治疗效果:(1)破坏细菌代谢稳态,从而克服生物膜对传统抗菌药物的固有抗性,以及(2)激活细胞免疫以有效对抗细菌免疫逃逸机制。通过代谢和免疫途径打破生物膜耐受性,我们的策略能够使铜离子深入渗透到生物膜中,并在小鼠植入物感染和腹膜炎感染模型中有效清除感染。我们的方法通过诱导细菌类铜死亡样死亡和激活细胞免疫,引入了一种生物膜耐受性破坏方法,为对抗生物膜感染提供了一种有前景的策略。