Ni Chang, Li Xisheng, Jiang Haiye, Gui Shumin, Yin Heng, Nie Xinmin
Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan Province, China.
Mater Today Bio. 2025 Jan 9;31:101470. doi: 10.1016/j.mtbio.2025.101470. eCollection 2025 Apr.
infection is the most common pathogen in burn wound infections, causing delayed wound healing and progression to chronic wounds. Therefore, there is an urgent need to develop antimicrobial agents that can promote wound healing for effectively treating infected wounds.
Using magnetic stirring and ultrasound to synthesize Apt-pM@UCNPmSiO-Cur-CAZ. The nanosystems were characterized using transmission electron microscopy (TEM), dynamic light scattering (DLS), and ultraviolet-visible spectrophotometry (UV-Vis). Flow cytometry, bacterial LIVE/DEAD staining and scanning electron microscopy were performed to assess the in vitro antibacterial and anti-biofilm effects of the nanosystems. The wound healing potential and in vivo toxicity of the nanosystems were evaluated in a mouse skin wound model.
The Apt-pM@UCNPmSiO-Cur-CAZ synthesized exhibited uniform circular shape with a Zeta potential of -0.8 mV. In vitro, Apt-pM@UCNPmSiO-Cur-CAZ demonstrated superior antibacterial effects compared to standalone antibiotics. Bacteria treated with Apt-pM@UCNPmSiO-Cur-CAZ showed varying degrees of deformation and shrinkage, resulting in severe damage to the bacterial cells. Additionally, Apt-pM@UCNPmSiO-Cur-CAZ can inhibit and eradicate bacterial biofilms, while also targeting bacteria for enhanced antibacterial efficacy. Interestingly, the NIR light could enhance the antibacterial and anti-biofilm effects of Apt-pM@UCNPmSiO-Cur-CAZ due to the photodynamic action. In a mouse skin wound infection model, the nanosystem effectively eliminated wound bacteria, promoting the healing of -infected wounds without significant toxic effects.
Apt-pM@UCNPmSiO-Cur-CAZ is a novel targeted nano-delivery system with promising potential in combating infections, and it may serve as a new therapeutic approach for treating skin wound infections.
金黄色葡萄球菌是烧伤创面感染中最常见的病原菌,可导致创面愈合延迟并进展为慢性创面。因此,迫切需要开发能够促进创面愈合的抗菌剂,以有效治疗感染创面。
采用磁力搅拌和超声合成Apt-pM@UCNPmSiO-Cur-CAZ。利用透射电子显微镜(TEM)、动态光散射(DLS)和紫外可见分光光度法(UV-Vis)对纳米系统进行表征。进行流式细胞术、细菌活/死染色和扫描电子显微镜检查,以评估纳米系统的体外抗菌和抗生物膜效果。在小鼠皮肤创面模型中评估纳米系统的创面愈合潜力和体内毒性。
合成的Apt-pM@UCNPmSiO-Cur-CAZ呈均匀圆形,Zeta电位为-0.8 mV。在体外,Apt-pM@UCNPmSiO-Cur-CAZ与单独使用抗生素相比表现出优异的抗菌效果。用Apt-pM@UCNPmSiO-Cur-CAZ处理的细菌显示出不同程度的变形和收缩,导致细菌细胞严重受损。此外,Apt-pM@UCNPmSiO-Cur-CAZ可以抑制和根除细菌生物膜,同时还能靶向细菌以增强抗菌效果。有趣的是,近红外光由于光动力作用可增强Apt-pM@UCNPmSiO-Cur-CAZ的抗菌和抗生物膜效果。在小鼠皮肤创面感染模型中,该纳米系统有效消除了创面细菌,促进了感染创面的愈合,且无明显毒性作用。
Apt-pM@UCNPmSiO-Cur-CAZ是一种新型靶向纳米递送系统,在对抗金黄色葡萄球菌感染方面具有广阔的应用前景,可能成为治疗皮肤创面感染的一种新的治疗方法。