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Preparation and Evaluation of the Antibacterial Effect of Magnetic Nanoparticles Containing Gentamicin: A Preliminary In vitro Study

BACKGROUND: Magnetic nanoparticles (MNPs) loaded by various active compounds can be used for targeted drug delivery. Objectives: In the present study, the Fe(3)O(4) magnetic nanoparticles that contained gentamicin were prepared and their antibacterial activities were studied. MATERIALS AND METHODS:...

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Detalles Bibliográficos
Autores principales: Douzandeh-Mobarrez, Banafsheh, Ansari-Dogaheh, Mehdi, Eslaminejad, Touba, Kazemipour, Maryam, Shakibaie, Mojtaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Genetic Engineering and Biotechnology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697835/
https://www.ncbi.nlm.nih.gov/pubmed/31457030
http://dx.doi.org/10.21859/ijb.1559
Descripción
Sumario:BACKGROUND: Magnetic nanoparticles (MNPs) loaded by various active compounds can be used for targeted drug delivery. Objectives: In the present study, the Fe(3)O(4) magnetic nanoparticles that contained gentamicin were prepared and their antibacterial activities were studied. MATERIALS AND METHODS: MNPs containing gentamicin (G@SA-MNPs) were prepared using sodium alginate (SA) as a surface modifier. After and before coating, the prepared MNPs were characterized using transmission electron microscopy (TEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM). Finally, the antibacterial effect of the MNPs was investigated by a conventional serial agar dilution method. RESULTS: Particle size distribution analysis showed that the size of MNPs, before and after coating, was in the range of 1–18 nm and 12–40 nm, respectively. The magnetization curve of G@SA-MNPs (with saturation magnetization of 27.9 emu.g(-1)) confirmed ferromagnetic property. Loading gentamicin on the surface of MNPs was qualitatively verified by FTIR spectrum. Quantitative analysis measurements indicated the gentamicin loading on SA-MNPs as 56.7 ± 5.4%. The measured MICs of G@SA-MNPs for Pseudomonas aeruginosa (PTTC 1574) was 1.28 µg.mL(-1). The sub-MIC (0.64 µg.mL(-1)) concentration of G@SA-MNPs in nutrient broth could successfully inhibit the growth of P. aeruginosa for 14 hours. CONCLUSIONS: Loading gentamicin on the SA-MNPs exhibited reasonable antibacterial effects against P. aeruginosa.