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Abstract
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.
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1 Monash University, Department of Materials Science and Engineering, Faculty of Engineering, Clayton, Australia (GRID:grid.1002.3) (ISNI:0000 0004 1936 7857)
2 Monash University, Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Clayton, Australia (GRID:grid.1002.3) (ISNI:0000 0004 1936 7857)
3 Monash University, Department of Materials Science and Engineering, Faculty of Engineering, Clayton, Australia (GRID:grid.1002.3) (ISNI:0000 0004 1936 7857); Monash University, Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Clayton, Australia (GRID:grid.1002.3) (ISNI:0000 0004 1936 7857)
4 Monash University, Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Clayton, Australia (GRID:grid.1002.3) (ISNI:0000 0004 1936 7857)
5 Australian Nuclear Science and Technology Organisation, Australian Centre for Neutron Scattering, Kirrawee DC, Australia (GRID:grid.1089.0) (ISNI:0000 0004 0432 8812)
6 Australian Nuclear Science and Technology Organisation, Australian Centre for Neutron Scattering, Kirrawee DC, Australia (GRID:grid.1089.0) (ISNI:0000 0004 0432 8812); National Synchrotron Radiation Research Center, Hsinchu, Taiwan (GRID:grid.410766.2) (ISNI:0000 0001 0749 1496)
7 City University of Hong Kong, School of Energy and Environment & Department of Materials Science and Engineering, Hong Kong, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846); Shenzhen Research Institute of City University of Hong Kong, Shenzhen, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846)
8 CSIRO Manufacturing, Clayton, Australia (GRID:grid.494571.a)