纳米材料
吸附
化学
金黄色葡萄球菌
病毒
金属有机骨架
法维皮拉维
抗菌剂
药物输送
耐甲氧西林金黄色葡萄球菌
纳米技术
组合化学
材料科学
病毒学
细菌
有机化学
传染病(医学专业)
2019年冠状病毒病(COVID-19)
生物
医学
疾病
病理
遗传学
作者
Mengyuan Xu,Xi Li,Huiying Zheng,Jiehan Chen,Xiaohua Ye,Tiantian Liu
出处
期刊:Molecules
[MDPI AG]
日期:2022-03-31
卷期号:27 (7): 2288-2288
被引量:13
标识
DOI:10.3390/molecules27072288
摘要
Nanomaterial technology has attracted much attention because of its antibacterial and drug delivery properties, among other applications. Metal-organic frameworks (MOFs) have advantages, such as their pore structure, large specific surface area, open metal sites, and chemical stability, over other nanomaterials, enabling better drug encapsulation and adsorption. In two examples, we used the common pathogenic bacterium Staphylococcus aureus and highly infectious influenza A virus. A novel complex MIL-101(Fe)-T705 was formed by synthesizing MOF material MIL-101(Fe) with the drug favipiravir (T-705), and a hot solvent synthesis method was applied to investigate the in vitro antibacterial and antiviral activities. The results showed that MIL-101(Fe)-T705 combined the advantages of nanomaterials and drugs and could inhibit the growth of Staphylococcus aureus at a concentration of 0.0032 g/mL. Regarding the inhibition of influenza A virus, MIL-101(Fe)-T705 showed good biosafety at 12, 24, 48, and 72 h in addition to a good antiviral effect at concentrations of 0.1, 0.2, 0.4, 0.8, 1.6, and 3 μg/mL, which were higher than MIL-101(Fe) and T-705.
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