
pmid: 27232956
Infections caused by antibiotic-resistant pathogens, particularly Gram-negative bacteria, represent significant treatment challenges for physicians resulting in high rates of morbidity and mortality. The outer membrane of Gram-negative bacteria acts as a permeability barrier to many compounds that would otherwise be effective antibacterial agents, including those effective against Gram-positive pathogens. Potentiator molecules disrupt this barrier allowing entry of otherwise impermeant molecules, thus providing a strategy to render multi-drug resistant pathogens susceptible to a broader range of antibiotics. Potentiator molecules are cationic and the mechanism of disruption involves interaction with the negatively charged outer membrane. This physical attribute, along with an often high degree of lipophilicity typically endears these molecules with unacceptable toxicity. Presented herein are examples of advanced potentiator molecules being evaluated for use in combination therapy for the treatment of resistant Gram-negative infections.
Cell Membrane Permeability, Cell Membrane, Drug Synergism, Microbial Sensitivity Tests, Anti-Bacterial Agents, Drug Resistance, Multiple, Bacterial, Gram-Negative Bacteria, Drug Therapy, Combination, Polymyxins, Gram-Negative Bacterial Infections, Antimicrobial Cationic Peptides
Cell Membrane Permeability, Cell Membrane, Drug Synergism, Microbial Sensitivity Tests, Anti-Bacterial Agents, Drug Resistance, Multiple, Bacterial, Gram-Negative Bacteria, Drug Therapy, Combination, Polymyxins, Gram-Negative Bacterial Infections, Antimicrobial Cationic Peptides
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