A polytherapy based approach to combat antimicrobial resistance using cubosomes

被引:39
|
作者
Lai, Xiangfeng [1 ]
Han, Mei-Ling [2 ,3 ]
Ding, Yue [1 ,4 ,5 ]
Chow, Seong Hoong [4 ,5 ]
Le Brun, Anton P. [6 ]
Wu, Chun-Ming [6 ,7 ]
Bergen, Phillip J. [2 ,3 ]
Jiang, Jhih-hang [2 ,3 ]
Hsu, Hsien-Yi [8 ,9 ,10 ]
Muir, Benjamin W. [11 ]
White, Jacinta [11 ]
Song, Jiangning [4 ,5 ]
Li, Jian [2 ,3 ]
Shen, Hsin-Hui [1 ,4 ,5 ]
机构
[1] Monash Univ, Fac Engn, Dept Mat Sci & Engn, Clayton, Vic 3800, Australia
[2] Monash Univ, Infect & Immun Program, Monash Biomed Discovery Inst, Clayton, Vic 3800, Australia
[3] Monash Univ, Dept Microbiol, Clayton, Vic 3800, Australia
[4] Monash Univ, Biomed Discovery Inst, Clayton, Vic 3800, Australia
[5] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[6] Australian Nucl Sci & Technol Org, Australian Ctr Neutron Scattering, Locked Bag 2001, Kirrawee Dc, NSW 2232, Australia
[7] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[8] City Univ Hong Kong, Sch Energy & Environm, Kowloon Tong, Hong Kong, Peoples R China
[9] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon Tong, Hong Kong, Peoples R China
[10] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
[11] CSIRO Mfg, Clayton, Vic 3168, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
POLYMYXIN-B; IN-VITRO; ACINETOBACTER-BAUMANNII; PSEUDOMONAS-AERUGINOSA; COMBINATIONS; PEPTIDES; COLISTIN; PHOSPHATIDYLSERINE; PHARMACODYNAMICS; TEMPERATURE;
D O I
10.1038/s41467-022-28012-5
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
A depleted antimicrobial drug pipeline combined with an increasing prevalence of Gram-negative 'superbugs' has increased interest in nano therapies to treat antibiotic resistance. As cubosomes and polymyxins disrupt the outer membrane of Gram-negative bacteria via different mechanisms, we herein examine the antimicrobial activity of polymyxin-loaded cubosomes and explore an alternative strategy via the polytherapy treatment of pathogens with cubosomes in combination with polymyxin. The polytherapy treatment substantially increases antimicrobial activity compared to polymyxin B-loaded cubosomes or polymyxin and cubosomes alone. Confocal microscopy and neutron reflectometry suggest the superior polytherapy activity is achieved via a two-step process. Firstly, electrostatic interactions between polymyxin and lipid A initially destabilize the outer membrane. Subsequently, an influx of cubosomes results in further membrane disruption via a lipid exchange process. These findings demonstrate that nanoparticle-based polytherapy treatments may potentially serve as improved alternatives to the conventional use of drug-loaded lipid nanoparticles for the treatment of "superbugs". An increasing prevalence of Gram-negative bacteria increases the interest in nanotherapies to treat antibiotic resistance. Here, the authors examine the antimicrobial activity of polymyxin-loaded cubosomes and explore a polytherapy treatment of pathogens with cubosomes in combination with polymyxin.
引用
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页数:12
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