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Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites

BACKGROUND: Chitin nanofibers sheets (CNFSs) with nanoscale fiber-like surface structures are nontoxic and biodegradable biomaterials with large surface-to-mass ratio. CNFSs are widely applied as biomedical materials such as a functional wound dressing. This study aimed to develop antimicrobial biom...

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Autores principales: Nguyen, Vinh Quang, Ishihara, Masayuki, Kinoda, Jun, Hattori, Hidemi, Nakamura, Shingo, Ono, Takeshi, Miyahira, Yasushi, Matsui, Takemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263038/
https://www.ncbi.nlm.nih.gov/pubmed/25467525
http://dx.doi.org/10.1186/s12951-014-0049-1
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author Nguyen, Vinh Quang
Ishihara, Masayuki
Kinoda, Jun
Hattori, Hidemi
Nakamura, Shingo
Ono, Takeshi
Miyahira, Yasushi
Matsui, Takemi
author_facet Nguyen, Vinh Quang
Ishihara, Masayuki
Kinoda, Jun
Hattori, Hidemi
Nakamura, Shingo
Ono, Takeshi
Miyahira, Yasushi
Matsui, Takemi
author_sort Nguyen, Vinh Quang
collection PubMed
description BACKGROUND: Chitin nanofibers sheets (CNFSs) with nanoscale fiber-like surface structures are nontoxic and biodegradable biomaterials with large surface-to-mass ratio. CNFSs are widely applied as biomedical materials such as a functional wound dressing. This study aimed to develop antimicrobial biomaterials made up of CNFS-immobilized silver nanoparticles (CNFS/Ag NPs). MATERIALS AND METHODS: CNFSs were immersed in suspensions of Ag NPs (5.17 ± 1.9 nm in diameter; mean ± SD) for 30 min at room temperature to produce CNFS/Ag NPs. CNFS/Ag NPs were characterized by transmission electron microscopy (TEM) and then tested for antimicrobial activities against Escherichia (E.) coli, Pseudomonas (P.) aeruginosa, and H1N1 influenza A virus, three pathogens that represent the most widespread infectious bacteria and viruses. Ultrathin sectioning of bacterial cells also was carried out to observe the bactericidal mechanism of Ag NPs. RESULTS: The TEM images indicated that the Ag NPs are dispersed and tightly adsorbed onto CNFSs. Although CNFSs alone have only weak antimicrobial activity, CNFS/Ag NPs showed much stronger antimicrobial properties against E. coli, P. aeruginosa, and influenza A virus, with the amount of immobilized Ag NPs onto CNFSs. CONCLUSIONS: Our results suggest that CNFS/Ag NPs interacting with those microbes exhibit stronger antimicrobial activities, and that it is possible to apply CNFS/Ag NPs as anti-virus sheets as well as anti-infectious wound dressings.
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spelling pubmed-42630382014-12-12 Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites Nguyen, Vinh Quang Ishihara, Masayuki Kinoda, Jun Hattori, Hidemi Nakamura, Shingo Ono, Takeshi Miyahira, Yasushi Matsui, Takemi J Nanobiotechnology Research BACKGROUND: Chitin nanofibers sheets (CNFSs) with nanoscale fiber-like surface structures are nontoxic and biodegradable biomaterials with large surface-to-mass ratio. CNFSs are widely applied as biomedical materials such as a functional wound dressing. This study aimed to develop antimicrobial biomaterials made up of CNFS-immobilized silver nanoparticles (CNFS/Ag NPs). MATERIALS AND METHODS: CNFSs were immersed in suspensions of Ag NPs (5.17 ± 1.9 nm in diameter; mean ± SD) for 30 min at room temperature to produce CNFS/Ag NPs. CNFS/Ag NPs were characterized by transmission electron microscopy (TEM) and then tested for antimicrobial activities against Escherichia (E.) coli, Pseudomonas (P.) aeruginosa, and H1N1 influenza A virus, three pathogens that represent the most widespread infectious bacteria and viruses. Ultrathin sectioning of bacterial cells also was carried out to observe the bactericidal mechanism of Ag NPs. RESULTS: The TEM images indicated that the Ag NPs are dispersed and tightly adsorbed onto CNFSs. Although CNFSs alone have only weak antimicrobial activity, CNFS/Ag NPs showed much stronger antimicrobial properties against E. coli, P. aeruginosa, and influenza A virus, with the amount of immobilized Ag NPs onto CNFSs. CONCLUSIONS: Our results suggest that CNFS/Ag NPs interacting with those microbes exhibit stronger antimicrobial activities, and that it is possible to apply CNFS/Ag NPs as anti-virus sheets as well as anti-infectious wound dressings. BioMed Central 2014-12-03 /pmc/articles/PMC4263038/ /pubmed/25467525 http://dx.doi.org/10.1186/s12951-014-0049-1 Text en © Nguyen et al.; licensee BioMed Central Ltd. 2014 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Nguyen, Vinh Quang
Ishihara, Masayuki
Kinoda, Jun
Hattori, Hidemi
Nakamura, Shingo
Ono, Takeshi
Miyahira, Yasushi
Matsui, Takemi
Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title_full Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title_fullStr Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title_full_unstemmed Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title_short Development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
title_sort development of antimicrobial biomaterials produced from chitin-nanofiber sheet/silver nanoparticle composites
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263038/
https://www.ncbi.nlm.nih.gov/pubmed/25467525
http://dx.doi.org/10.1186/s12951-014-0049-1
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