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Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid

Bacterial infections have become a global issue that requires urgent attention, particularly regarding to emergence of multidrug resistant bacteria. We developed quaternary amine-containing antimicrobial poly(bile acid)s that contain a hydrophobic core of lithocholic acid in the main-chain. Interest...

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Detalles Bibliográficos
Autores principales: Ganewatta, Mitra S., Rahman, Md Anisur, Mercado, Louis, Shokfai, Tinom, Decho, Alan W., Reineke, Theresa M., Tang, Chuanbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935773/
https://www.ncbi.nlm.nih.gov/pubmed/29744456
http://dx.doi.org/10.1016/j.bioactmat.2018.02.001
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author Ganewatta, Mitra S.
Rahman, Md Anisur
Mercado, Louis
Shokfai, Tinom
Decho, Alan W.
Reineke, Theresa M.
Tang, Chuanbing
author_facet Ganewatta, Mitra S.
Rahman, Md Anisur
Mercado, Louis
Shokfai, Tinom
Decho, Alan W.
Reineke, Theresa M.
Tang, Chuanbing
author_sort Ganewatta, Mitra S.
collection PubMed
description Bacterial infections have become a global issue that requires urgent attention, particularly regarding to emergence of multidrug resistant bacteria. We developed quaternary amine-containing antimicrobial poly(bile acid)s that contain a hydrophobic core of lithocholic acid in the main-chain. Interestingly, by choosing appropriate monomers, these cationic polymers can form core-shell micelles. These polymers exhibited biocidal activity against both Gram-positive and Gram-negative bacterial species. It is demonstrated that the micelles can deliver hydrophobic antibiotics that functionally have dual antimicrobial activities. Cytotoxicity assays against HeLa cells showed dosage-dependent toxicity for polymers with longer linkers.
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spelling pubmed-59357732018-05-09 Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid Ganewatta, Mitra S. Rahman, Md Anisur Mercado, Louis Shokfai, Tinom Decho, Alan W. Reineke, Theresa M. Tang, Chuanbing Bioact Mater Article Bacterial infections have become a global issue that requires urgent attention, particularly regarding to emergence of multidrug resistant bacteria. We developed quaternary amine-containing antimicrobial poly(bile acid)s that contain a hydrophobic core of lithocholic acid in the main-chain. Interestingly, by choosing appropriate monomers, these cationic polymers can form core-shell micelles. These polymers exhibited biocidal activity against both Gram-positive and Gram-negative bacterial species. It is demonstrated that the micelles can deliver hydrophobic antibiotics that functionally have dual antimicrobial activities. Cytotoxicity assays against HeLa cells showed dosage-dependent toxicity for polymers with longer linkers. KeAi Publishing 2018-02-23 /pmc/articles/PMC5935773/ /pubmed/29744456 http://dx.doi.org/10.1016/j.bioactmat.2018.02.001 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ganewatta, Mitra S.
Rahman, Md Anisur
Mercado, Louis
Shokfai, Tinom
Decho, Alan W.
Reineke, Theresa M.
Tang, Chuanbing
Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title_full Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title_fullStr Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title_full_unstemmed Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title_short Facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
title_sort facially amphiphilic polyionene biocidal polymers derived from lithocholic acid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935773/
https://www.ncbi.nlm.nih.gov/pubmed/29744456
http://dx.doi.org/10.1016/j.bioactmat.2018.02.001
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