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Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens

Advances in nanotechnology have demonstrated potential application of nanoparticles for effective and targeted drug delivery. Here, we investigated the antimicrobial and immunological properties and the feasibility of using nanoparticles to deliver antimicrobial agents to treat a cutaneous pathogen....

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Detalles Bibliográficos
Autores principales: Friedman, Adam J, Phan, Jenny, Schairer, David, Champer, Jackson, Qin, Min, Pirouz, Aslan, Blecher, Karin, Oren, Ami, Liu, Phil, Modlin, Robert L, Kim, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631294/
https://www.ncbi.nlm.nih.gov/pubmed/23190896
http://dx.doi.org/10.1038/jid.2012.399
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author Friedman, Adam J
Phan, Jenny
Schairer, David
Champer, Jackson
Qin, Min
Pirouz, Aslan
Blecher, Karin
Oren, Ami
Liu, Phil
Modlin, Robert L
Kim, Jenny
author_facet Friedman, Adam J
Phan, Jenny
Schairer, David
Champer, Jackson
Qin, Min
Pirouz, Aslan
Blecher, Karin
Oren, Ami
Liu, Phil
Modlin, Robert L
Kim, Jenny
author_sort Friedman, Adam J
collection PubMed
description Advances in nanotechnology have demonstrated potential application of nanoparticles for effective and targeted drug delivery. Here, we investigated the antimicrobial and immunological properties and the feasibility of using nanoparticles to deliver antimicrobial agents to treat a cutaneous pathogen. Nanoparticles synthesized with chitosan and alginate demonstrated a direct antimicrobial activity in vitro against Propionibacterium acnes, the bacterium linked to the pathogenesis of acne. By electron microscopy imaging, chitosan-alginate nanoparticles were found to induce disruption of the P. acnes cell membrane, providing a mechanism for the bactericidal effect. The chitosan-alginate nanoparticles also exhibited anti-inflammatory properties as they inhibited P. acnes induced inflammatory cytokine production in human monocytes and keratinocytes. Furthermore, benzoyl peroxide, a commonly used anti-acne drug, was effectively encapsulated in the chitosan-alginate nanoparticles and demonstrated superior antimicrobial activity against P. acnes compared to benzoyl peroxide alone while demonstrating less toxicity to eukaryotic cells. Together, these data suggest the potential utility of topical delivery of chitosan-alginate nanoparticle encapsulated drug therapy for the treatment of dermatologic conditions with infectious and inflammatory components.
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spelling pubmed-36312942013-11-01 Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens Friedman, Adam J Phan, Jenny Schairer, David Champer, Jackson Qin, Min Pirouz, Aslan Blecher, Karin Oren, Ami Liu, Phil Modlin, Robert L Kim, Jenny J Invest Dermatol Article Advances in nanotechnology have demonstrated potential application of nanoparticles for effective and targeted drug delivery. Here, we investigated the antimicrobial and immunological properties and the feasibility of using nanoparticles to deliver antimicrobial agents to treat a cutaneous pathogen. Nanoparticles synthesized with chitosan and alginate demonstrated a direct antimicrobial activity in vitro against Propionibacterium acnes, the bacterium linked to the pathogenesis of acne. By electron microscopy imaging, chitosan-alginate nanoparticles were found to induce disruption of the P. acnes cell membrane, providing a mechanism for the bactericidal effect. The chitosan-alginate nanoparticles also exhibited anti-inflammatory properties as they inhibited P. acnes induced inflammatory cytokine production in human monocytes and keratinocytes. Furthermore, benzoyl peroxide, a commonly used anti-acne drug, was effectively encapsulated in the chitosan-alginate nanoparticles and demonstrated superior antimicrobial activity against P. acnes compared to benzoyl peroxide alone while demonstrating less toxicity to eukaryotic cells. Together, these data suggest the potential utility of topical delivery of chitosan-alginate nanoparticle encapsulated drug therapy for the treatment of dermatologic conditions with infectious and inflammatory components. 2012-11-29 2013-05 /pmc/articles/PMC3631294/ /pubmed/23190896 http://dx.doi.org/10.1038/jid.2012.399 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Friedman, Adam J
Phan, Jenny
Schairer, David
Champer, Jackson
Qin, Min
Pirouz, Aslan
Blecher, Karin
Oren, Ami
Liu, Phil
Modlin, Robert L
Kim, Jenny
Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title_full Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title_fullStr Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title_full_unstemmed Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title_short Antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
title_sort antimicrobial and anti-inflammatory activity of chitosan-alginate nanoparticles: a targeted therapy for cutaneous pathogens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631294/
https://www.ncbi.nlm.nih.gov/pubmed/23190896
http://dx.doi.org/10.1038/jid.2012.399
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