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Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides
Antimicrobial biopolymers provide a biodegradable, sustainable, safe, and cheap approach to drug delivery and wound dressing to control bacterial infection and improve wound healing respectively. Here, we report a one-step method of making antimicrobial alginate polymer from sodium alginate and aque...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435147/ https://www.ncbi.nlm.nih.gov/pubmed/30913239 http://dx.doi.org/10.1371/journal.pone.0214411 |
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author | Kumar, Lokender Brice, John Toberer, Linda Klein-Seetharaman, Judith Knauss, Daniel Sarkar, Susanta K. |
author_facet | Kumar, Lokender Brice, John Toberer, Linda Klein-Seetharaman, Judith Knauss, Daniel Sarkar, Susanta K. |
author_sort | Kumar, Lokender |
collection | PubMed |
description | Antimicrobial biopolymers provide a biodegradable, sustainable, safe, and cheap approach to drug delivery and wound dressing to control bacterial infection and improve wound healing respectively. Here, we report a one-step method of making antimicrobial alginate polymer from sodium alginate and aqueous extract of Wakame using antibiotic aminoglycosides. Thin layer chromatography of commercially available sodium alginate and Wakame extract showed similar oligosaccharide profiles. Screening of six aminoglycosides showed that kanamycin disulfate and neomycin sulfate produces the highest amount of biopolymer; however, kanamycin disulfate produces the most malleable and form fitting biopolymer. Image texture analysis of biopolymers showed similar quantification parameters for all the six aminoglycosides. Weight of alginate polymer as a function of aminoglycoside concentration follows a growth model of prion protein, consistent with the aggregating nature of both processes. Slow release of antibiotics and the resulting zone of inhibition against E. coli DH5α were observed by agar well diffusion assay. Inexpensive method of production and slow release of antibiotics will enable diverse applications of antimicrobial alginate biopolymer reported in this paper. |
format | Online Article Text |
id | pubmed-6435147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64351472019-04-08 Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides Kumar, Lokender Brice, John Toberer, Linda Klein-Seetharaman, Judith Knauss, Daniel Sarkar, Susanta K. PLoS One Research Article Antimicrobial biopolymers provide a biodegradable, sustainable, safe, and cheap approach to drug delivery and wound dressing to control bacterial infection and improve wound healing respectively. Here, we report a one-step method of making antimicrobial alginate polymer from sodium alginate and aqueous extract of Wakame using antibiotic aminoglycosides. Thin layer chromatography of commercially available sodium alginate and Wakame extract showed similar oligosaccharide profiles. Screening of six aminoglycosides showed that kanamycin disulfate and neomycin sulfate produces the highest amount of biopolymer; however, kanamycin disulfate produces the most malleable and form fitting biopolymer. Image texture analysis of biopolymers showed similar quantification parameters for all the six aminoglycosides. Weight of alginate polymer as a function of aminoglycoside concentration follows a growth model of prion protein, consistent with the aggregating nature of both processes. Slow release of antibiotics and the resulting zone of inhibition against E. coli DH5α were observed by agar well diffusion assay. Inexpensive method of production and slow release of antibiotics will enable diverse applications of antimicrobial alginate biopolymer reported in this paper. Public Library of Science 2019-03-26 /pmc/articles/PMC6435147/ /pubmed/30913239 http://dx.doi.org/10.1371/journal.pone.0214411 Text en © 2019 Kumar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kumar, Lokender Brice, John Toberer, Linda Klein-Seetharaman, Judith Knauss, Daniel Sarkar, Susanta K. Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title | Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title_full | Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title_fullStr | Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title_full_unstemmed | Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title_short | Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
title_sort | antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435147/ https://www.ncbi.nlm.nih.gov/pubmed/30913239 http://dx.doi.org/10.1371/journal.pone.0214411 |
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