Biodegradable cationic ε-poly-L-lysine-conjugated polymeric nanoparticles as a new effective antibacterial agent

被引:37
作者
Zhao, Ruifang [1 ,2 ]
Wang, Hai [1 ]
Ji, Tianjiao [1 ]
Anderson, Greg [3 ]
Nie, Guangjun [1 ]
Zhao, Yuliang [1 ]
机构
[1] Chinese Acad Sci, Natl Ctr Nanosci & Technol, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] Queensland Inst Med Res, Royal Brisbane Hosp, Herston, Qld 4029, Australia
基金
中国国家自然科学基金;
关键词
EPL-PCL copolymers; Biodegradable cationic nanoparticles; Broad-spectrum antibacterial activity; Disruption of bacterial walls/membranes; Cell invagination; MATERNO-FETAL TRANSFER; ALKALINE-PHOSPHATASE; CELL-DEATH; POLY(EPSILON-CAPROLACTONE); INFLAMMATION; NANOSPHERES; MECHANISM; PEPTIDES; DELIVERY; SILVER;
D O I
10.1007/s11434-014-0704-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Biocompatible and biodegradable epsilon-poly-L-lysine (EPL)/poly (epsilon-caprolactone) (PCL) copolymer was designed and synthesized. The amphiphilic EPL-PCL copolymer could easily self-assembled into monodispersed nanoparticles (NPs), which showed a broad-spectrum antibacterial activity against Escherichia coli, Staphylococcus aureus and Bacillus subtilis. Interestingly, the antibacterial efficacy of the novel NPs is more potent than the cationic peptide EPL. To explore the underlying mechanism of the biodegradable cationic NPs, various possible antibacterial pathways have been validated. The NPs have been found that they can disrupt bacterial walls/membranes and induce the increasing in reactive oxygen species and alkaline phosphatase levels. More importantly, the self-assembled NPs induced the changes in bacterial osmotic pressure, resulting in cell invagination to form holes and cause the leakage of cytoplasm. Taken together, our results suggest that the EPL-PCL NPs can be further developed to be a promising antimicrobial agent to treat infectious diseases as surfactants and emulsifiers to enhance drug encapsulation efficiency and antimicrobial activity.
引用
收藏
页码:216 / 226
页数:11
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