Cargando…
Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis
BACKGROUND: Although assemblies of hydrophobic-modified bacitracin A with PLGA (Nano-BA(PLGA)) have demonstrated promising antibacterial activities against both Gram-positive and Gram-negative bacteria, the desirable antibacterial potency has remained challenging due to the low solubility of Nano-BA...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131780/ https://www.ncbi.nlm.nih.gov/pubmed/30205822 http://dx.doi.org/10.1186/s12951-018-0397-3 |
_version_ | 1783354191945662464 |
---|---|
author | Hong, Wei Liu, Lipeng Zhao, Yining Liu, Yinghui Zhang, Dexian Liu, Mingchun |
author_facet | Hong, Wei Liu, Lipeng Zhao, Yining Liu, Yinghui Zhang, Dexian Liu, Mingchun |
author_sort | Hong, Wei |
collection | PubMed |
description | BACKGROUND: Although assemblies of hydrophobic-modified bacitracin A with PLGA (Nano-BA(PLGA)) have demonstrated promising antibacterial activities against both Gram-positive and Gram-negative bacteria, the desirable antibacterial potency has remained challenging due to the low solubility of Nano-BA(PLGA). To address this tissue, a series of Pluronic copolymers (Pluronic(®) F127, Pluronic(®) P123 and Pluronic(®) P85) were selected to link the N-terminus of bacitracin A to construct Pluronic-based nano-self assemblies (Nano-BA(F127), Nano-BA(P123) and Nano-BA(P85)). RESULTS: Impressively, all the newly designed Pluronic-based Nano-BAs possessed higher solubility and stronger effectiveness against both Gram-positive and Gram-negative bacteria compared with Nano-BA(PLGA), especially the modification with Pluronic(®) P85. Surface tension measurements indicated that Nano-BA(P85) was much more tensioactive than Nano-BA(PLGA), which usually translated into a good membranolytic effect. Fluorescence spectroscopy and electron microscopy analyses confirmed the speculation that the cell wall/membrane might be the main action target of Nano-BA(P85) by permeabilizing the cell membrane and damaging the membrane integrity. In vivo results further demonstrated that Nano-BA(P85) significantly suppressed bacterial growth and prolonged survival time in the bacterial peritonitis mouse model with negligible toxicity. CONCLUSIONS: Collectively, the membrane targeting mechanism of action is entirely distinct from those of clinically used antibacterial agents. Furthermore, the new approach of construction nanoantibiotics based on the modification of commercially available antibiotics with Pluronic copolymers is demonstrated to have an efficient therapeutic effect against bacterial infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0397-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6131780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61317802018-09-13 Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis Hong, Wei Liu, Lipeng Zhao, Yining Liu, Yinghui Zhang, Dexian Liu, Mingchun J Nanobiotechnology Research BACKGROUND: Although assemblies of hydrophobic-modified bacitracin A with PLGA (Nano-BA(PLGA)) have demonstrated promising antibacterial activities against both Gram-positive and Gram-negative bacteria, the desirable antibacterial potency has remained challenging due to the low solubility of Nano-BA(PLGA). To address this tissue, a series of Pluronic copolymers (Pluronic(®) F127, Pluronic(®) P123 and Pluronic(®) P85) were selected to link the N-terminus of bacitracin A to construct Pluronic-based nano-self assemblies (Nano-BA(F127), Nano-BA(P123) and Nano-BA(P85)). RESULTS: Impressively, all the newly designed Pluronic-based Nano-BAs possessed higher solubility and stronger effectiveness against both Gram-positive and Gram-negative bacteria compared with Nano-BA(PLGA), especially the modification with Pluronic(®) P85. Surface tension measurements indicated that Nano-BA(P85) was much more tensioactive than Nano-BA(PLGA), which usually translated into a good membranolytic effect. Fluorescence spectroscopy and electron microscopy analyses confirmed the speculation that the cell wall/membrane might be the main action target of Nano-BA(P85) by permeabilizing the cell membrane and damaging the membrane integrity. In vivo results further demonstrated that Nano-BA(P85) significantly suppressed bacterial growth and prolonged survival time in the bacterial peritonitis mouse model with negligible toxicity. CONCLUSIONS: Collectively, the membrane targeting mechanism of action is entirely distinct from those of clinically used antibacterial agents. Furthermore, the new approach of construction nanoantibiotics based on the modification of commercially available antibiotics with Pluronic copolymers is demonstrated to have an efficient therapeutic effect against bacterial infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0397-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-11 /pmc/articles/PMC6131780/ /pubmed/30205822 http://dx.doi.org/10.1186/s12951-018-0397-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Hong, Wei Liu, Lipeng Zhao, Yining Liu, Yinghui Zhang, Dexian Liu, Mingchun Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title | Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title_full | Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title_fullStr | Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title_full_unstemmed | Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title_short | Pluronic-based nano-self-assemblies of bacitracin A with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
title_sort | pluronic-based nano-self-assemblies of bacitracin a with a new mechanism of action for an efficient in vivo therapeutic effect against bacterial peritonitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131780/ https://www.ncbi.nlm.nih.gov/pubmed/30205822 http://dx.doi.org/10.1186/s12951-018-0397-3 |
work_keys_str_mv | AT hongwei pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis AT liulipeng pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis AT zhaoyining pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis AT liuyinghui pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis AT zhangdexian pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis AT liumingchun pluronicbasednanoselfassembliesofbacitracinawithanewmechanismofactionforanefficientinvivotherapeuticeffectagainstbacterialperitonitis |