金黄色葡萄球菌
抗生素
大肠杆菌
铁
程序性细胞死亡
抗菌活性
微生物学
伤口愈合
细菌
细胞生长
致病菌
细胞凋亡
化学
生物
免疫学
生物化学
基因
有机化学
遗传学
作者
Ying Zhou,Chongyang Cai,Cheng Wang,Guoming Hu,Yuting Li,Mengjiao Han,Shen Hu,Pu Cheng
出处
期刊:Drug Delivery
[Taylor & Francis]
日期:2022-12-01
卷期号:30 (1): 1-8
被引量:16
标识
DOI:10.1080/10717544.2022.2152134
摘要
Skin infection is a major health issue that usually is caused by the continuous proliferation of bacteria in wounds. With the abuse of antibiotics worldwide, the battle against skin infection is becoming more and more difficult. Therefore, the development of new ways with different antibacterial mechanisms to current antibiotics is urgently needed. Inspired by the powerful inhibition of ferroptosis used in cancer therapy, here in our study, ferric-loaded lipid nanoparticles (Fe-LNPs) with unform size (∼130 nm) and surface charge (∼12 mV) were constructed and found to effectively inhibit the growth of both Gram positive (Staphylococcus aureus, S. aureus) and negative (Escherichia coli, E. coli) strains, possibly due to induction of ferroptosis-like cell death mechanisms. Most importantly, Fe-LNPs can also effectively inhibit the proliferation of S. aureus in a skin infection model and promote the healing of wounds. The Fe-LNPs can be applied as a powerful antibacterial formulation for future application in clinic.
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