Cargando…
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....
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1782266778338983936 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3631294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT friedmanadamj antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT phanjenny antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT schairerdavid antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT champerjackson antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT qinmin antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT pirouzaslan antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT blecherkarin antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT orenami antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT liuphil antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT modlinrobertl antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens AT kimjenny antimicrobialandantiinflammatoryactivityofchitosanalginatenanoparticlesatargetedtherapyforcutaneouspathogens |