Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment

Metallic nanoparticles, such as gold nanoparticles (AuNPs), have been extensively studied as drug delivery systems for various therapeutic applications. However, drug-loaded-AuNPs have been rarely explored in vivo for their effect on bacteria residing inside tissues. Ciprofloxacin (CIP) is a second-...

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Autores principales: Afrah Nawaz, Syed Mohsin Ali, Nosheen Fatima Rana, Tahreem Tanweer, Amna Batool, Thomas J. Webster, Farid Menaa, Sundus Riaz, Zahra Rehman, Farhat Batool, Misha Fatima, Tuba Maryam, Iqra Shafique, Abida Saleem, Arfa Iqbal
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/7f99b42ed573444ca15045685459abb1
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spelling oai:doaj.org-article:7f99b42ed573444ca15045685459abb12021-11-25T18:32:51ZCiprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment10.3390/nano111131522079-4991https://doaj.org/article/7f99b42ed573444ca15045685459abb12021-11-01T00:00:00Zhttps://www.mdpi.com/2079-4991/11/11/3152https://doaj.org/toc/2079-4991Metallic nanoparticles, such as gold nanoparticles (AuNPs), have been extensively studied as drug delivery systems for various therapeutic applications. However, drug-loaded-AuNPs have been rarely explored in vivo for their effect on bacteria residing inside tissues. Ciprofloxacin (CIP) is a second-generation fluoroquinolone with a broad-spectrum of antibiotic properties devoid of developing bacteria resistance. This research is focused on the synthesis and physical characterization of Ciprofloxacin-loaded gold nanoparticles (CIP-AuNPs) and their effect on the colonization of <i>Enterococcus faecalis</i> in the liver and kidneys of mice. The successfully prepared CIP-AuNPs were stable and exerted enhanced in vitro antibacterial activity against <i>E. faecalis</i> compared with free CIP. The optimized CIP-AuNPs were administered (500 µg/Kg) once a day via tail vein to infected mice for eight days and were found to be effective in eradicating <i>E. faecalis</i> from the host tissues. Moreover, unlike CIP, CIP-AuNPs were non-hemolytic. In summary, this study demonstrated that CIP-AuNPs are promising and biocompatible alternative therapeutics for <i>E.-faecalis</i>-induced infections resistant to conventional drugs (e.g., beta-lactams and vancomycin) and should be further investigated.Afrah NawazSyed Mohsin AliNosheen Fatima RanaTahreem TanweerAmna BatoolThomas J. WebsterFarid MenaaSundus RiazZahra RehmanFarhat BatoolMisha FatimaTuba MaryamIqra ShafiqueAbida SaleemArfa IqbalMDPI AGarticledrug deliveryantibioticsantimicrobial resistancegold nanoparticlesciprofloxacin<i>Enterococcus faecalis</i>ChemistryQD1-999ENNanomaterials, Vol 11, Iss 3152, p 3152 (2021)
institution DOAJ
collection DOAJ
language EN
topic drug delivery
antibiotics
antimicrobial resistance
gold nanoparticles
ciprofloxacin
<i>Enterococcus faecalis</i>
Chemistry
QD1-999
spellingShingle drug delivery
antibiotics
antimicrobial resistance
gold nanoparticles
ciprofloxacin
<i>Enterococcus faecalis</i>
Chemistry
QD1-999
Afrah Nawaz
Syed Mohsin Ali
Nosheen Fatima Rana
Tahreem Tanweer
Amna Batool
Thomas J. Webster
Farid Menaa
Sundus Riaz
Zahra Rehman
Farhat Batool
Misha Fatima
Tuba Maryam
Iqra Shafique
Abida Saleem
Arfa Iqbal
Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
description Metallic nanoparticles, such as gold nanoparticles (AuNPs), have been extensively studied as drug delivery systems for various therapeutic applications. However, drug-loaded-AuNPs have been rarely explored in vivo for their effect on bacteria residing inside tissues. Ciprofloxacin (CIP) is a second-generation fluoroquinolone with a broad-spectrum of antibiotic properties devoid of developing bacteria resistance. This research is focused on the synthesis and physical characterization of Ciprofloxacin-loaded gold nanoparticles (CIP-AuNPs) and their effect on the colonization of <i>Enterococcus faecalis</i> in the liver and kidneys of mice. The successfully prepared CIP-AuNPs were stable and exerted enhanced in vitro antibacterial activity against <i>E. faecalis</i> compared with free CIP. The optimized CIP-AuNPs were administered (500 µg/Kg) once a day via tail vein to infected mice for eight days and were found to be effective in eradicating <i>E. faecalis</i> from the host tissues. Moreover, unlike CIP, CIP-AuNPs were non-hemolytic. In summary, this study demonstrated that CIP-AuNPs are promising and biocompatible alternative therapeutics for <i>E.-faecalis</i>-induced infections resistant to conventional drugs (e.g., beta-lactams and vancomycin) and should be further investigated.
format article
author Afrah Nawaz
Syed Mohsin Ali
Nosheen Fatima Rana
Tahreem Tanweer
Amna Batool
Thomas J. Webster
Farid Menaa
Sundus Riaz
Zahra Rehman
Farhat Batool
Misha Fatima
Tuba Maryam
Iqra Shafique
Abida Saleem
Arfa Iqbal
author_facet Afrah Nawaz
Syed Mohsin Ali
Nosheen Fatima Rana
Tahreem Tanweer
Amna Batool
Thomas J. Webster
Farid Menaa
Sundus Riaz
Zahra Rehman
Farhat Batool
Misha Fatima
Tuba Maryam
Iqra Shafique
Abida Saleem
Arfa Iqbal
author_sort Afrah Nawaz
title Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
title_short Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
title_full Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
title_fullStr Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
title_full_unstemmed Ciprofloxacin-Loaded Gold Nanoparticles against Antimicrobial Resistance: An In Vivo Assessment
title_sort ciprofloxacin-loaded gold nanoparticles against antimicrobial resistance: an in vivo assessment
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/7f99b42ed573444ca15045685459abb1
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