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Bactericidal Peptidomimetic Polyurethanes with Remarkable Selectivity against Escherichia coli.
Mankoci, Steven; Kaiser, Ricky L; Sahai, Nita; Barton, Hazel A; Joy, Abraham.
Afiliação
  • Mankoci S; Department of Polymer Science and ‡Department of Biology, The University of Akron, Akron, Ohio 44325, United States.
  • Kaiser RL; Department of Polymer Science and Department of Biology, The University of Akron, Akron, Ohio 44325, United States.
  • Sahai N; Department of Polymer Science and Department of Biology, The University of Akron, Akron, Ohio 44325, United States.
  • Barton HA; Department of Polymer Science and Department of Biology, The University of Akron, Akron, Ohio 44325, United States.
  • Joy A; Department of Polymer Science and Department of Biology, The University of Akron, Akron, Ohio 44325, United States.
ACS Biomater Sci Eng ; 3(10): 2588-2597, 2017 Oct 09.
Article em En | MEDLINE | ID: mdl-33465913
The increasing incidence of drug-resistant strains of bacteria necessitates the development of new classes of antimicrobials. Host defense peptides, also known as antimicrobial peptides, are promising in this regard but have several drawbacks. Herein, we show that peptidomimetic polyurethanes with pendant functional groups that mimic lysine and valine amino acid residues have high antibacterial activity against Gram negative Escherichia coli, yet are less effective against Gram positive Staphylococcus aureus. All the polyurethanes designed in this study display high bactericidal activity against E. coli, whereas the polyurethanes with high concentrations of lysine mimicking functional groups display minimal cytotoxicity toward mammalian cells. Control experiments with pexiganan, an analogue of the host defense peptide magainin, showed that the polyurethanes described here have high bactericidal activity, while having comparable hemocompatibility and lower mammalian cell toxicity. Overall, the results point to an encouraging new class of peptidomimetic synthetic polymers with selective bactericidal activity to E. coli and low mammalian cell toxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Biomater Sci Eng Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Biomater Sci Eng Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos