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Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release

The magnetic targeting drug delivery system is an effective way of targeting therapy. In this study, the monodisperse Fe(3)O(4) nanoparticles with a particles size of about 180 nm were first prepared via a solvothermal method. Subsequently, the core-shell structure Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO...

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Detalles Bibliográficos
Autores principales: Shen, Lazhen, Li, Bei, Qiao, Yongsheng, Song, Jinping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427558/
https://www.ncbi.nlm.nih.gov/pubmed/30862125
http://dx.doi.org/10.3390/ma12050828
Descripción
Sumario:The magnetic targeting drug delivery system is an effective way of targeting therapy. In this study, the monodisperse Fe(3)O(4) nanoparticles with a particles size of about 180 nm were first prepared via a solvothermal method. Subsequently, the core-shell structure Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/polypyrrole (PPy) composite nanospheres were successfully synthesized by coating Fe(3)O(4) nanoparticles with SiO(2) shell layer using the Stöber method and PPy shell by solvothermal method in turn. The as-prepared nanoparticles were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM), thermogravimetric analysis (TGA), and Ultraviolet-Visible spectrophotometer (UV-Vis). The results indicated that the as-prepared composite nanospheres displayed a well-defined core-shell structure and monodispersity. The thicknesses of SiO(2) shell and PPy shell were ~6 nm and ~19 nm, respectively. Additionally, the as-prepared nanoparticles exhibited high saturation magnetization of 104 emu/g, 77 emu/g, and 24 emu/g, and have great potential applications in drug delivery. The drug loading and drug release of the Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy composite nanospheres to ibuprofen (IBU) under stirring and ultrasonication were investigated. Their drug loading efficiency and drug release efficiency under ultrasonication were all higher than 33% and 90%, respectively. The drug release analyses showed sustained release of IBU from nanospheres and followed the Korsmeyer-Peppas model.