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The Analysis of Chitosan-Coated Nanovesicles Containing Erythromycin-Characterization and Biocompatibility in Mice. | LitMetric

AI Article Synopsis

  • * This study focused on creating and analyzing chitosan-coated vesicles that carry erythromycin (ERT) and evaluating their safety in mice through various treatments.
  • * Findings reveal that oral administration of these chitosan liposomes containing ERT did not significantly alter blood components or organ functions, indicating good biocompatibility; histological reviews showed no harmful effects on liver or kidney structures, suggesting these liposomes could improve traditional ERT therapy.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698811PMC
http://dx.doi.org/10.3390/antibiotics10121471DOI Listing

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