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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Wei, Liu, Lipeng, Zhao, Yining, Liu, Yinghui, Zhang, Dexian, Liu, Mingchun
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