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The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice

Nanoantibiotics have proved improved pharmacokinetic characteristics and antimicrobial features. Recent studies have shown non-toxicity, non-immunogenicity, antioxidant, anti-hyperlipidemic, and hepatocyte protective actions, among other advantages of chitosan-based nanoparticles. The purpose of our...

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Autores principales: Hilițanu, Loredana Nicoleta, Mititelu-Tarțău, Liliana, Popa, Grațiela Eliza, Buca, Beatrice Rozalina, Pavel, Liliana Lăcrămioara, Pelin, Ana-Maria, Meca, Andreea-Daniela, Bogdan, Maria, Pricop, Daniela Angelica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698811/
https://www.ncbi.nlm.nih.gov/pubmed/34943683
http://dx.doi.org/10.3390/antibiotics10121471
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author Hilițanu, Loredana Nicoleta
Mititelu-Tarțău, Liliana
Popa, Grațiela Eliza
Buca, Beatrice Rozalina
Pavel, Liliana Lăcrămioara
Pelin, Ana-Maria
Meca, Andreea-Daniela
Bogdan, Maria
Pricop, Daniela Angelica
author_facet Hilițanu, Loredana Nicoleta
Mititelu-Tarțău, Liliana
Popa, Grațiela Eliza
Buca, Beatrice Rozalina
Pavel, Liliana Lăcrămioara
Pelin, Ana-Maria
Meca, Andreea-Daniela
Bogdan, Maria
Pricop, Daniela Angelica
author_sort Hilițanu, Loredana Nicoleta
collection PubMed
description Nanoantibiotics have proved improved pharmacokinetic characteristics and antimicrobial features. Recent studies have shown non-toxicity, non-immunogenicity, antioxidant, anti-hyperlipidemic, and hepatocyte protective actions, among other advantages of chitosan-based nanoparticles. The purpose of our study was the structural analysis of novel chitosan-coated vesicles entrapping erythromycin (ERT) and the assessment of their biocompatibility in mice. According to the group in which they were randomly assigned, the mice were treated orally with one of the following: distilled water; chitosan; ERT; chitosan vesicles containing ERT. Original nanosystems entrapping ERT in liposomes stabilized with chitosan were designed. Their oral administration did not produce sizeable modifications in the percentages of the leukocyte formula elements, of some blood constants useful for evaluating the hepatic and renal function, respectively, and of some markers of oxidative stress and immune system activity, which suggests a good biocompatibility in mice. The histological examination did not reveal significant alterations of liver and kidney architecture in mice treated with chitosan liposomes entrapping ERT. The results indicate the designed liposomes are a promising approach to overcome disadvantages of conventional ERT treatments and to amplify their benefits and can be further studied as carrier systems.
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spelling pubmed-86988112021-12-24 The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice Hilițanu, Loredana Nicoleta Mititelu-Tarțău, Liliana Popa, Grațiela Eliza Buca, Beatrice Rozalina Pavel, Liliana Lăcrămioara Pelin, Ana-Maria Meca, Andreea-Daniela Bogdan, Maria Pricop, Daniela Angelica Antibiotics (Basel) Article Nanoantibiotics have proved improved pharmacokinetic characteristics and antimicrobial features. Recent studies have shown non-toxicity, non-immunogenicity, antioxidant, anti-hyperlipidemic, and hepatocyte protective actions, among other advantages of chitosan-based nanoparticles. The purpose of our study was the structural analysis of novel chitosan-coated vesicles entrapping erythromycin (ERT) and the assessment of their biocompatibility in mice. According to the group in which they were randomly assigned, the mice were treated orally with one of the following: distilled water; chitosan; ERT; chitosan vesicles containing ERT. Original nanosystems entrapping ERT in liposomes stabilized with chitosan were designed. Their oral administration did not produce sizeable modifications in the percentages of the leukocyte formula elements, of some blood constants useful for evaluating the hepatic and renal function, respectively, and of some markers of oxidative stress and immune system activity, which suggests a good biocompatibility in mice. The histological examination did not reveal significant alterations of liver and kidney architecture in mice treated with chitosan liposomes entrapping ERT. The results indicate the designed liposomes are a promising approach to overcome disadvantages of conventional ERT treatments and to amplify their benefits and can be further studied as carrier systems. MDPI 2021-11-30 /pmc/articles/PMC8698811/ /pubmed/34943683 http://dx.doi.org/10.3390/antibiotics10121471 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hilițanu, Loredana Nicoleta
Mititelu-Tarțău, Liliana
Popa, Grațiela Eliza
Buca, Beatrice Rozalina
Pavel, Liliana Lăcrămioara
Pelin, Ana-Maria
Meca, Andreea-Daniela
Bogdan, Maria
Pricop, Daniela Angelica
The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title_full The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title_fullStr The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title_full_unstemmed The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title_short The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin—Characterization and Biocompatibility in Mice
title_sort analysis of chitosan-coated nanovesicles containing erythromycin—characterization and biocompatibility in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698811/
https://www.ncbi.nlm.nih.gov/pubmed/34943683
http://dx.doi.org/10.3390/antibiotics10121471
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