头孢唑林
金黄色葡萄球菌
大肠杆菌
微生物学
抗菌活性
抗菌剂
银纳米粒子
化学
最小抑制浓度
最低杀菌浓度
碘化丙啶
细菌
生物
抗生素
生物化学
材料科学
纳米颗粒
纳米技术
遗传学
基因
细胞凋亡
程序性细胞死亡
作者
Aiman Batool,Mercy Chepngetich Bore,Jingwen Wu,Chaoyu Li,Hongjuan Zeng
标识
DOI:10.1016/j.jddst.2023.104550
摘要
Antibacterial drug resistance is a growing challenge that can be dealt with by introducing novel drugs or improving the efficacy of existing drugs. Combining nanomaterials with existing drugs to enhance drug effectiveness has garnered substantial research attention. Herein, we evaluated the synergistic antibacterial potential of cefazolin and silver nanoparticles (AgNPs) against two resistant strains of bacteria, Escherichia coli (ATCC35218) and Staphylococcus aureus (ATCC6538P). The broth macrodilution method and the Time-Kill assay were used to determine the antibacterial potential of the AgNP-Cefazolin combination. The Propidium Iodide Assay (PIA) and Bicinchoninic acid assay (BCA) were performed to examine the bacterial damage. Both strains showed the same minimum inhibitory concentration (MIC) of 400 μg/ml for cefazolin alone. When combined with AgNPs, both strains observed a significant MIC decrease. AgNPs to cefazolin ratio of 0.063:300 μg/ml exhibited the best antimicrobial activity against Staphylococcus aureus and Escherichia coli. PIA exhibited much fluorescence when cefazolin and AgNPs were used together, indicating significant damage to bacterial cell walls and membranes. Similarly, BCA showed leakage of a considerable amount of bacterial cytoplasmic protein in the media. Our results show that using AgNPs and cefazolin together could be a promising nano-drug against the two tested strains.
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