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Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity
BACKGROUND: The ubiquitous nature of bacterial biofilms combined with the enhanced resistance towards antimicrobials has led to the development of an increasing number of strategies for biofilm eradication. Such strategies must take into account the existence of extracellular polymeric substances, w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045376/ https://www.ncbi.nlm.nih.gov/pubmed/33849570 http://dx.doi.org/10.1186/s12951-021-00851-2 |
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author | Barros, Caio H. N. Hiebner, Dishon W. Fulaz, Stephanie Vitale, Stefania Quinn, Laura Casey, Eoin |
author_facet | Barros, Caio H. N. Hiebner, Dishon W. Fulaz, Stephanie Vitale, Stefania Quinn, Laura Casey, Eoin |
author_sort | Barros, Caio H. N. |
collection | PubMed |
description | BACKGROUND: The ubiquitous nature of bacterial biofilms combined with the enhanced resistance towards antimicrobials has led to the development of an increasing number of strategies for biofilm eradication. Such strategies must take into account the existence of extracellular polymeric substances, which obstruct the diffusion of antibiofilm agents and assists in the maintenance of a well-defended microbial community. Within this context, nanoparticles have been studied for their drug delivery efficacy and easily customised surface. Nevertheless, there usually is a requirement for nanocarriers to be used in association with an antimicrobial agent; the intrinsically antimicrobial nanoparticles are most often made of metals or metal oxides, which is not ideal from ecological and biomedical perspectives. Based on this, the use of polymeric micelles as nanocarriers is appealing as they can be easily prepared using biodegradable organic materials. RESULTS: In the present work, micelles comprised of poly(lactic-co-glycolic acid) and dextran are prepared and then functionalised with curcumin. The effect of the functionalisation in the micelle’s physical properties was elucidated, and the antibacterial and antibiofilm activities were assessed for the prepared polymeric nanoparticles against Pseudomonas spp. cells and biofilms. It was found that the nanoparticles have good penetration into the biofilms, which resulted in enhanced antibacterial activity of the conjugated micelles when compared to free curcumin. Furthermore, the curcumin-functionalised micelles were efficient at disrupting mature biofilms and demonstrated antibacterial activity towards biofilm-embedded cells. CONCLUSION: Curcumin-functionalised poly(lactic-co-glycolic acid)-dextran micelles are novel nanostructures with an intrinsic antibacterial activity tested against two Pseudomonas spp. strains that have the potential to be further exploited to deliver a secondary bioactive molecule within its core. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00851-2. |
format | Online Article Text |
id | pubmed-8045376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80453762021-04-14 Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity Barros, Caio H. N. Hiebner, Dishon W. Fulaz, Stephanie Vitale, Stefania Quinn, Laura Casey, Eoin J Nanobiotechnology Research BACKGROUND: The ubiquitous nature of bacterial biofilms combined with the enhanced resistance towards antimicrobials has led to the development of an increasing number of strategies for biofilm eradication. Such strategies must take into account the existence of extracellular polymeric substances, which obstruct the diffusion of antibiofilm agents and assists in the maintenance of a well-defended microbial community. Within this context, nanoparticles have been studied for their drug delivery efficacy and easily customised surface. Nevertheless, there usually is a requirement for nanocarriers to be used in association with an antimicrobial agent; the intrinsically antimicrobial nanoparticles are most often made of metals or metal oxides, which is not ideal from ecological and biomedical perspectives. Based on this, the use of polymeric micelles as nanocarriers is appealing as they can be easily prepared using biodegradable organic materials. RESULTS: In the present work, micelles comprised of poly(lactic-co-glycolic acid) and dextran are prepared and then functionalised with curcumin. The effect of the functionalisation in the micelle’s physical properties was elucidated, and the antibacterial and antibiofilm activities were assessed for the prepared polymeric nanoparticles against Pseudomonas spp. cells and biofilms. It was found that the nanoparticles have good penetration into the biofilms, which resulted in enhanced antibacterial activity of the conjugated micelles when compared to free curcumin. Furthermore, the curcumin-functionalised micelles were efficient at disrupting mature biofilms and demonstrated antibacterial activity towards biofilm-embedded cells. CONCLUSION: Curcumin-functionalised poly(lactic-co-glycolic acid)-dextran micelles are novel nanostructures with an intrinsic antibacterial activity tested against two Pseudomonas spp. strains that have the potential to be further exploited to deliver a secondary bioactive molecule within its core. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00851-2. BioMed Central 2021-04-13 /pmc/articles/PMC8045376/ /pubmed/33849570 http://dx.doi.org/10.1186/s12951-021-00851-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Barros, Caio H. N. Hiebner, Dishon W. Fulaz, Stephanie Vitale, Stefania Quinn, Laura Casey, Eoin Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title | Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title_full | Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title_fullStr | Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title_full_unstemmed | Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title_short | Synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
title_sort | synthesis and self-assembly of curcumin-modified amphiphilic polymeric micelles with antibacterial activity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045376/ https://www.ncbi.nlm.nih.gov/pubmed/33849570 http://dx.doi.org/10.1186/s12951-021-00851-2 |
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