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

• Published in: Antibiotics (Basel) Vol. 10; no. 12; p. 1471
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 30.11.2021; MDPI
• Subjects: Acne; Antibiotics; Antiinfectives and antibacterials; Antioxidants; Bacteria; Bioavailability; Biocompatibility; Chitosan; Coated vesicles; Distilled water; Drug delivery systems; Erythromycin; Experiments; Gonorrhea; Immune system; Immunogenicity; Laboratory animals; Leukocytes; Lipids; Liposomes; Medical research; mice; Nanoparticles; Nanotechnology; nanovesicles; Oral administration; Oxidative stress; Pharmacokinetics; Pharmacy; Pneumonia; R&D; Renal function; Research & development; Structural analysis; Toxicity; Vesicles; Germany; Romania; chitosan; nanovesicles; biocompatibility; mice; erythromycin
• ISSN: 2079-6382; 2079-6382
• DOI: 10.3390/antibiotics10121471

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.