抗生素
微生物学
药品
金黄色葡萄球菌
抗生素耐药性
药物输送
核酸
化学
生物
细菌
药理学
生物化学
遗传学
有机化学
作者
Yue Sun,Xingyu Chen,Sirong Shi,Taoran Tian,Zhi-Qiang Liu,En Luo,Yunfeng Lin
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2023-02-01
卷期号:24 (2): 1052-1060
被引量:4
标识
DOI:10.1021/acs.biomac.2c01525
摘要
Antibiotic multiresistance (AMR) has emerged as a major threat to human health as millions of people die from AMR-related problems every year. As has been witnessed during the global COVID-19 pandemic, the significantly increased demand for antibiotics has aggravated the issue of AMR. Therefore, there is an urgent need to find ways to alleviate it. Tetrahedral framework nucleic acids (tFNAs) are novel nanomaterials that are often used as drug delivery platforms because of their structural diversity. This study formed a tFNAs-antibiotic compound (TAC) which has a strong growth inhibitory effect on Escherichia coli and methicillin-resistant Staphylococcus aureus (MRSA) in vitro owing to the increased absorption of antibiotics by bacteria and improved drug movement across cell membranes. We established a mouse model of systemic peritonitis and local wound infections. The TAC exhibited good biosafety and improved the survival rate of severely infected mice, promoting the healing of local infections. In addition to the better transport of antibiotics to the target, the TAC may also enhance immunity by regulating the differentiation of M1 and M2 macrophages, providing a new option for the treatment of infections.
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