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Current Trends in Development of Liposomes for Targeting Bacterial Biofilms

Biofilm targeting represents a great challenge for effective antimicrobial therapy. Increased biofilm resistance, even with the elevated concentrations of very potent antimicrobial agents, often leads to failed therapeutic outcome. Application of biocompatible nanomicrobials, particularly liposomall...

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Detalles Bibliográficos
Autores principales: Rukavina, Zora, Vanić, Željka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932481/
https://www.ncbi.nlm.nih.gov/pubmed/27231933
http://dx.doi.org/10.3390/pharmaceutics8020018
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author Rukavina, Zora
Vanić, Željka
author_facet Rukavina, Zora
Vanić, Željka
author_sort Rukavina, Zora
collection PubMed
description Biofilm targeting represents a great challenge for effective antimicrobial therapy. Increased biofilm resistance, even with the elevated concentrations of very potent antimicrobial agents, often leads to failed therapeutic outcome. Application of biocompatible nanomicrobials, particularly liposomally-associated nanomicrobials, presents a promising approach for improved drug delivery to bacterial cells and biofilms. Versatile manipulations of liposomal physicochemical properties, such as the bilayer composition, membrane fluidity, size, surface charge and coating, enable development of liposomes with desired pharmacokinetic and pharmacodynamic profiles. This review attempts to provide an unbiased overview of investigations of liposomes destined to treat bacterial biofilms. Different strategies including the recent advancements in liposomal design aiming at eradication of existing biofilms and prevention of biofilm formation, as well as respective limitations, are discussed in more details.
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spelling pubmed-49324812016-07-13 Current Trends in Development of Liposomes for Targeting Bacterial Biofilms Rukavina, Zora Vanić, Željka Pharmaceutics Review Biofilm targeting represents a great challenge for effective antimicrobial therapy. Increased biofilm resistance, even with the elevated concentrations of very potent antimicrobial agents, often leads to failed therapeutic outcome. Application of biocompatible nanomicrobials, particularly liposomally-associated nanomicrobials, presents a promising approach for improved drug delivery to bacterial cells and biofilms. Versatile manipulations of liposomal physicochemical properties, such as the bilayer composition, membrane fluidity, size, surface charge and coating, enable development of liposomes with desired pharmacokinetic and pharmacodynamic profiles. This review attempts to provide an unbiased overview of investigations of liposomes destined to treat bacterial biofilms. Different strategies including the recent advancements in liposomal design aiming at eradication of existing biofilms and prevention of biofilm formation, as well as respective limitations, are discussed in more details. MDPI 2016-05-24 /pmc/articles/PMC4932481/ /pubmed/27231933 http://dx.doi.org/10.3390/pharmaceutics8020018 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rukavina, Zora
Vanić, Željka
Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title_full Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title_fullStr Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title_full_unstemmed Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title_short Current Trends in Development of Liposomes for Targeting Bacterial Biofilms
title_sort current trends in development of liposomes for targeting bacterial biofilms
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932481/
https://www.ncbi.nlm.nih.gov/pubmed/27231933
http://dx.doi.org/10.3390/pharmaceutics8020018
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