Affiliation:
1. Department of Chemistry and Biochemistry University of South Carolina Columbia SC 29208 USA
2. Department of Chemistry University of South Florida Tampa FL 33620 USA
3. Department of Pathology Microbiology and Immunology University of South Carolina School of Medicine Columbia SC 29209 USA
4. Department of Biochemistry and Molecular Biology Michigan State University East Lansing MI 48824 USA
Abstract
AbstractAmong multiple approaches to combating antimicrobial resistance, a combination therapy of existing antibiotics with bacterial membrane‐perturbing agents is promising. A viable platform of metallopolymers as adjuvants in combination with traditional antibiotics is reported in this work to combat both planktonic and stationary cells of Gram‐negative superbugs and their biofilms. Antibacterial efficacy, toxicity, antibiofilm activity, bacterial resistance propensity, and mechanisms of action of metallopolymer‐antibiotic combinations are investigated. These metallopolymers exhibit 4‐16‐fold potentiation of antibiotics against Gram‐negative bacteria with negligible toxicity toward mammalian cells. More importantly, the lead combinations (polymer‐ceftazidime and polymer‐rifampicin) eradicate preformed biofilms of MDR E. coli and P. aeruginosa, respectively. Further, β‐lactamase inhibition, outer membrane permeabilization, and membrane depolarization demonstrate synergy of these adjuvants with different antibiotics. Moreover, the membrane‐active metallopolymers enable the antibiotics to circumvent bacterial resistance development. Altogether, the results indicate that such non‐antibiotic adjuvants bear the promise to revitalize the efficacy of existing antibiotics to tackle Gram‐negative bacterial infections.
Funder
National Institutes of Health
Subject
Pharmaceutical Science,Biomedical Engineering,Biomaterials
Cited by
7 articles.
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