基于mof的双刺激响应纳米系统协同光热/药物抗菌治疗

Ya Xiao, Meng-Ran Xu, Na Lv, Chen Cheng, Pei Huang, Jiabin Li, Yi Hu, Ming Sun
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引用次数: 1

摘要

耐药细菌病原体的严重威胁是由于过度使用抗生素而产生的。光热疗法(PTT)已成为突出的可行的替代策略,抗菌治疗。在这项工作中,我们报道了一种基于咪唑酸分子筛框架-8 (ZIF-8)的NIR/pH双刺激响应抗菌制剂,该制剂具有很强的抗菌活性,将光热加热与增强抗生素递送相结合。采用聚多巴胺(PDA)表面修饰的ZIF-8包封万古霉素,构建新型抗菌制剂(Van@ZIF-8@PDA)。这种治疗方法对革兰氏阳性耐万古霉素金黄色葡萄球菌Mu50进行了试验。结果表明,PDA涂层改善了ZIF-8的稳定性和分散性,同时具有较高的光热转换效率。近红外(NIR)光照射激活的热疗,结合ph依赖性纳米颗粒降解释放万古霉素,能够严格控制药物输送,在生物膜形成之前和生物膜形成之前协同消除浮游细菌。我们发现这种组合制剂在破坏细胞结构的同时也降解细菌DNA。此外,进一步的研究表明Van@ZIF-8@PDA纳米颗粒具有良好的生物相容性,对宿主器官和组织的毒性低,同时也降低了有效控制细菌所需的抗生素浓度。最后,我们在小鼠皮肤脓肿模型中处理Mu50,发现Van@ZIF-8@PDA在体内有效且安全。总的来说,这项研究表明,这种基于NIR/pH双重刺激反应的纳米颗粒配方为临床应用提供了一种有希望的潜在策略,可以对抗细菌感染,从而绕过抗生素耐药性。
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Dual Stimuli-Responsive MOF-Based Nanosystem for Synergistic Photothermal/Pharmacological Antibacterial Therapy
The serious threat of drug-resistant bacterial pathogens has arisen through overuse of antibiotics. Photothermal therapy (PTT) has come to prominence as viable alternative strategy for antibacterial therapy. In this work, we report a NIR/pH dual stimuli-responsive antibacterial formulation based on zeolitic imidazolate frameworks-8 (ZIF-8) with strong antibacterial activity that combines photothermal heating with enhanced antibiotic delivery. ZIF-8 with polydopamine (PDA) surface modification was used to encapsulate the antibiotic vancomycin to construct a novel antimicrobial formulation (Van@ZIF-8@PDA). This treatment was tested against Gram-positive vancomycin-resistant Staphylococcus aureus Mu50. Results showed that the PDA coating improved ZIF-8 stability and dispersion, while also conferring a high photothermal conversion efficiency. Hyperthermia activated by near-infrared (NIR) light irradiation, in conjunction with pH-dependent nanoparticle degradation to release vancomycin, enabled tight control of drug delivery that functioned synergistically in the elimination of both planktonic bacteria prior to biofilm formation and established biofilms. We found that this combined formulation compromises cell structure while also degrading bacterial DNA. Moreover, further investigation showed that the Van@ZIF-8@PDA nanoparticles exhibit excellent biocompatibility, with low toxicity toward host organs and tissues, while also reducing the antibiotic concentration needed for effective bacterial control. Finally, we treated Mu50 in a mouse model of skin abscess and found that Van@ZIF-8@PDA was effective and safe in vivo. Cumulatively, this study shows that this NIR/pH dual stimuli-responsive nanoparticle-based formulation offers a promising potential strategy for clinical application against bacterial infection that circumvents antibiotic resistance.
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