内化
金黄色葡萄球菌
细胞毒性
抗菌剂
细胞内
化学
抗菌活性
细菌细胞结构
肽
庆大霉素
细胞
纳米颗粒
PLGA公司
细菌
微生物学
抗生素
生物化学
纳米技术
体外
材料科学
生物
遗传学
有机化学
作者
Bin Ma,Gan Hu,Shuangshuang Guo,Qi Zeng,Yue Chen,Deog Hwan Oh,Yongguo Jin,Xing Fu
标识
DOI:10.1016/j.foodres.2022.111638
摘要
Bacterial pathogens have posed a serious threat to human health because they are difficult to be eliminated inside cells. Here, an effective design of poly(lactic-co-glycolic) (PLGA) nanoparticles (NPs) modified with antimicrobial peptides and loaded with gentamicin (Gen) was reported with enhanced antibacterial activity and cellular internalization ability. The results showed that the drug loading capacity and encapsulation efficiency of OVTp12-modified NPs were 7.55 % and 81.3 %, respectively. We observed that OVTp12 and OVTp12-modified NPs significantly increased the interaction with Staphylococcus aureus cells. Moreover, OVTp12-modified NPs showed an effective inhibitory effect on S. aureus with low cytotoxicity. The results of cell internalization indicated that OVTp12-modified NPs were markedly higher than that of unmodified nanoparticles when incubated with MC3T3-E1 cells. In conclusion, the bacterial cell-targeting ability of this antimicrobial peptide provides advantages for the treatment of intracellular bacterial infections.
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