Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, Jinan University, Guangzhou 510632, China.
J Mater Chem B. 2024 May 29;12(21):5111-5127. doi: 10.1039/d4tb00536h.
Recently, bacterial infections have become a global crisis, greatly threatening the health of human beings. The development of a non-antibiotic biomaterial is recognized as an alternative way for the effective treatment of bacterial infections. In the present work, a multifunctional copper peroxide (CP) nanodot-decorated gold nanostar (GNS)/silica nanorod (SiNR) Janus nanostructure (GNS@CP/SiNR) with excellent antibacterial activity was reported. Due to the formation of the Janus nanostructure, GNS@CP/SiNR displayed strong plasmonic resonance absorbance in the near infrared (NIR)-II region that enabled the nanosystem to achieve mild photothermal therapy (MPTT). In acidic conditions, CP decorated on GNS@CP/SiNR dissociated rapidly by releasing Cu and HO, which subsequently transformed to ˙OH the Fenton-like reaction for chemodynamic therapy (CDT). As a result, GNS@CP/SiNR could effectively inhibit both Gram-negative () and Gram-positive (), and eradicate the associated bacterial biofilms by exerting the synergistic MPTT/CDT antibacterial effect. Moreover, GNS@CP/SiNR was also demonstrated to be effective in treating wound infections, as verified on the -infected full thickness excision wound rat model. Our mechanism study revealed that the synergistic MPTT/CDT effect of GNS@CP/SiNR firstly caused bacterial membrane damage, followed by boosting intracellular ROS the severe oxidative stress effect, which subsequently caused the depletion of intracellular GSH and DNA damage, finally leading to the death of bacteria.
最近,细菌感染已成为全球性危机,极大地威胁着人类健康。开发非抗生素生物材料被认为是有效治疗细菌感染的一种替代方法。在本工作中,报道了一种具有优异抗菌活性的多功能过氧化铜(CP)纳米点修饰的金纳米星(GNS)/硅纳米棒(SiNR)Janus 纳米结构(GNS@CP/SiNR)。由于形成了 Janus 纳米结构,GNS@CP/SiNR 在近红外(NIR-II)区域显示出强烈的等离子体共振吸收,使纳米系统能够实现温和的光热治疗(MPTT)。在酸性条件下,CP 迅速从 GNS@CP/SiNR 上解离,释放出 Cu 和 HO,随后转化为 ˙OH,进行芬顿样反应以实现化学动力学治疗(CDT)。因此,GNS@CP/SiNR 能够通过发挥协同 MPTT/CDT 抗菌作用有效抑制革兰氏阴性菌()和革兰氏阳性菌(),并消除相关的细菌生物膜。此外,GNS@CP/SiNR 还被证明在治疗感染方面是有效的,在 -感染的全层切除伤大鼠模型中得到了验证。我们的机制研究表明,GNS@CP/SiNR 的协同 MPTT/CDT 效应首先导致细菌膜损伤,随后增强细胞内 ROS 产生严重的氧化应激效应,进而导致细胞内 GSH 耗竭和 DNA 损伤,最终导致细菌死亡。