Li Yuange, Xue Song, Min Hong Sung, Chen Chen, Lu Liheng, Chen Zhiheng, Shan Haojie, Yin Fuli, Yu Xiaowei
Department of Orthopaedics, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, P. R. China.
Shanghai Institute of Traumatology and Orthopedics, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, P. R. China.
Adv Healthc Mater. 2025 Jul;14(19):e2500964. doi: 10.1002/adhm.202500964. Epub 2025 May 27.
The formation of bacterial biofilms presents a major challenge in infection treatments. Antimicrobial photodynamic therapy (aPDT) typically employs photosensitizers to generate reactive oxygen species (ROS) under irradiation, causing oxidative damage to both bacteria and biofilms. While prior studies have explored the integration of PDT with various other approaches, magnetic hyperthermia therapy (MHT) has not adequately addressed. To bridge this gap, a drug delivery system is designed that incorporates mesoporous FeO nanoparticles loaded with the photosensitizer IR-820, thereby combining aPDT with MHT. This system possesses magnetic-targeting capabilities, generates thermal energy when exposed to alternating magnetic fields, and facilitates the release of encapsulated IR-820. Furthermore, upon exposure to near-infrared light, IR-820 produces ROS. The synergistic effects of elevated temperature, degradation of the biofilm matrix, and enhanced ROS production effectively disrupted bacterial biofilms. This approach demonstrated promising antibacterial efficacy in both in vitro and in vivo, including in rat models of full-thickness infectious wound and subcutaneous abscesses. These results underscore the substantial potential of the system for future antibacterial applications.
细菌生物膜的形成给感染治疗带来了重大挑战。抗菌光动力疗法(aPDT)通常利用光敏剂在光照下产生活性氧(ROS),对细菌和生物膜造成氧化损伤。虽然先前的研究探索了光动力疗法与其他各种方法的结合,但磁热疗(MHT)尚未得到充分研究。为了填补这一空白,设计了一种药物递送系统,该系统包含负载有光敏剂IR-820的介孔FeO纳米颗粒,从而将aPDT与MHT相结合。该系统具有磁靶向能力,在交变磁场作用下产生热能,并促进封装的IR-820的释放。此外,在近红外光照射下,IR-820会产生活性氧。温度升高、生物膜基质降解和活性氧生成增加的协同作用有效地破坏了细菌生物膜。这种方法在体外和体内均显示出有前景的抗菌效果,包括在全层感染伤口和皮下脓肿的大鼠模型中。这些结果强调了该系统在未来抗菌应用中的巨大潜力。