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Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity

Infections caused by multidrug-resistant bacteria such as P. aeruginosa are important therapeutic complications. Piperacillin/Tazobactam is considered a safe antimicrobial agent. But we should not ignore the prevalence of resistant strains to this drug. In this work, a new polymeric micelle composed...

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Detalles Bibliográficos
Autores principales: Morteza, Milani, Roya, Salehi, Hamed, Hamishehkar, Amir, Zarebkohan, Abolfazl, Akbarzadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896493/
https://www.ncbi.nlm.nih.gov/pubmed/31797692
http://dx.doi.org/10.1080/10717544.2019.1693708
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author Morteza, Milani
Roya, Salehi
Hamed, Hamishehkar
Amir, Zarebkohan
Abolfazl, Akbarzadeh
author_facet Morteza, Milani
Roya, Salehi
Hamed, Hamishehkar
Amir, Zarebkohan
Abolfazl, Akbarzadeh
author_sort Morteza, Milani
collection PubMed
description Infections caused by multidrug-resistant bacteria such as P. aeruginosa are important therapeutic complications. Piperacillin/Tazobactam is considered a safe antimicrobial agent. But we should not ignore the prevalence of resistant strains to this drug. In this work, a new polymeric micelle composed of Piperacillin/Tazobactam-loaded Poly (ethylene glycol) methyl ether-block-poly (lactide-co-glycolide) (PLGA-PEG) was developed to improve the antimicrobial performance of P/T. The SEM and TEM studies of PLGA-PEG micelle showed, semi-spherical morphology with a mean diameter of below 30 nm. Zeta potential results indicated that the surface charge of PLGA-PEG micelle was −2.98 mV, while after encapsulation of P/T, the surface charge decreases to −4.13 mV. Clinical strains of P. aeruginosa were isolated and their resistance pattern against different antibiotics was evaluated. The MIC of free and P/T -Loaded PLGA-PEG micelles was determined. Also, the effect of free or P/T micelle against minimal biofilm eradication concentration and motility inhibition was evaluated. The bacterial isolates were resistant to most common antibiotics. The MIC of the free drug form and micelle form ranged from 4 to 512 µg/ml and 2 to 256 µg/ml, respectively. Generally, micelle showed more effective antibiofilm activities, inhibition of bacterial motility and reducing the MIC than that free drug form.
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spelling pubmed-68964932019-12-13 Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity Morteza, Milani Roya, Salehi Hamed, Hamishehkar Amir, Zarebkohan Abolfazl, Akbarzadeh Drug Deliv Research Article Infections caused by multidrug-resistant bacteria such as P. aeruginosa are important therapeutic complications. Piperacillin/Tazobactam is considered a safe antimicrobial agent. But we should not ignore the prevalence of resistant strains to this drug. In this work, a new polymeric micelle composed of Piperacillin/Tazobactam-loaded Poly (ethylene glycol) methyl ether-block-poly (lactide-co-glycolide) (PLGA-PEG) was developed to improve the antimicrobial performance of P/T. The SEM and TEM studies of PLGA-PEG micelle showed, semi-spherical morphology with a mean diameter of below 30 nm. Zeta potential results indicated that the surface charge of PLGA-PEG micelle was −2.98 mV, while after encapsulation of P/T, the surface charge decreases to −4.13 mV. Clinical strains of P. aeruginosa were isolated and their resistance pattern against different antibiotics was evaluated. The MIC of free and P/T -Loaded PLGA-PEG micelles was determined. Also, the effect of free or P/T micelle against minimal biofilm eradication concentration and motility inhibition was evaluated. The bacterial isolates were resistant to most common antibiotics. The MIC of the free drug form and micelle form ranged from 4 to 512 µg/ml and 2 to 256 µg/ml, respectively. Generally, micelle showed more effective antibiofilm activities, inhibition of bacterial motility and reducing the MIC than that free drug form. Taylor & Francis 2019-12-04 /pmc/articles/PMC6896493/ /pubmed/31797692 http://dx.doi.org/10.1080/10717544.2019.1693708 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Morteza, Milani
Roya, Salehi
Hamed, Hamishehkar
Amir, Zarebkohan
Abolfazl, Akbarzadeh
Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title_full Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title_fullStr Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title_full_unstemmed Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title_short Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
title_sort synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896493/
https://www.ncbi.nlm.nih.gov/pubmed/31797692
http://dx.doi.org/10.1080/10717544.2019.1693708
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