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Biocompatible Fe(3)O(4) Increases the Efficacy of Amoxicillin Delivery against Gram-Positive and Gram-Negative Bacteria

This paper reports the synthesis and characterization of amoxicillin- functionalized magnetite nanostructures (Fe(3)O(4)@AMO), revealing and discussing several biomedical applications of these nanomaterials. Our results proved that 10 nm Fe(3)O(4)@AMO nanoparticles does not alter the normal cell cyc...

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Detalles Bibliográficos
Autores principales: Grumezescu, Alexandru Mihai, Cartelle Gestal, Monica, Holban, Alina Maria, Grumezescu, Valentina, Vasile, Bogdan Ștefan, Mogoantă, Laurențiu, Iordache, Florin, Bleotu, Coralia, Mogoșanu, George Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270688/
https://www.ncbi.nlm.nih.gov/pubmed/24759068
http://dx.doi.org/10.3390/molecules19045013
Descripción
Sumario:This paper reports the synthesis and characterization of amoxicillin- functionalized magnetite nanostructures (Fe(3)O(4)@AMO), revealing and discussing several biomedical applications of these nanomaterials. Our results proved that 10 nm Fe(3)O(4)@AMO nanoparticles does not alter the normal cell cycle progression of cultured diploid cells, and an in vivo murine model confirms that the nanostructures disperse through the host body and tend to localize in particular sites and organs. The nanoparticles were found clustered especially in the lungs, kidneys and spleen, next to the blood vessels at this level, while being totally absent in the brain and liver, suggesting that they are circulated through the blood flow and have low toxicity. Fe(3)O(4)@AMO has the ability to be easily circulated through the body and optimizations may be done so these nanostructures cluster to a specific target region. Functionalized magnetite nanostructures proved a great antimicrobial effect, being active against both the Gram positive pathogen S. aureus and the Gram negative pathogen E. coli. The fabricated nanostructures significantly reduced the minimum inhibitory concentration (MIC) of the active drug. This result has a great practical relevance, since the functionalized nanostructures may be used for decreasing the therapeutic doses which usually manifest great severe side effects, when administrated in high doses. Fe(3)O(4)@AMO represents also a suitable approach for the development of new alternative strategies for improving the activity of therapeutic agents by targeted delivery and controlled release.