2011
DOI: 10.1128/aac.01516-10
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Antimicrobial Peptoids Are Effective against Pseudomonas aeruginosa Biofilms

Abstract: The resistance of biofilms to conventional antibiotics complicates the treatment of chronic cystic fibrosis (CF). We investigated the effects of peptoids, peptides, and conventional antibiotics on the biomass and cell viability within Pseudomonas aeruginosa biofilms. At their MICs, peptoids 1 and 1-C13 4mer caused maximum reductions in biomass and cell viability, respectively. These results suggest that peptoids of this class could be worth exploring for the treatment of pulmonary infections occurring in CF pa… Show more

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Cited by 119 publications
(101 citation statements)
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“…It is thought that the peptoid 1-C134mer, which has an hydrophobic tail and is active against P. aeruginosa biofilms, interacts strongly with and disrupt the hydrophobic matrix due to its surfactant like nature, facilitating deeper penetration (Kapoor et al 2011).…”
Section: Anti-biofilm Antimicrobial Peptide Strategiesmentioning
confidence: 99%
“…It is thought that the peptoid 1-C134mer, which has an hydrophobic tail and is active against P. aeruginosa biofilms, interacts strongly with and disrupt the hydrophobic matrix due to its surfactant like nature, facilitating deeper penetration (Kapoor et al 2011).…”
Section: Anti-biofilm Antimicrobial Peptide Strategiesmentioning
confidence: 99%
“…For the most part of the last decade, Methicillin-resistant Staphylococcus aureus (MRSA) was the leading cause of HAIs in Ireland [3]. However, another bacterium, Pseudomonas aeruginosa, is of increasing concern worldwide with for example 200,000 HAIs directly related to that organism annually in the USA alone [4]. Bacteria such P. aeruginosa, Staphylococci and Escherichia coli that can exist in biofilms exhibit extreme resistance compared to planktonic or free moving bacteria as they are protected from the host's immune cells and from the action of antimicrobial agents.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, we have developed mimics of AMPs using peptoids (poly-N-substituted glycines), which are protease-resistant (15) isomers of peptides ( Fig. 1) with broad-spectrum antibacterial activity comparable to, and in some cases better than, that of antimicrobial peptides (4,5,11,12,19).…”
mentioning
confidence: 99%