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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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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
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author Shen, Lazhen
Li, Bei
Qiao, Yongsheng
Song, Jinping
author_facet Shen, Lazhen
Li, Bei
Qiao, Yongsheng
Song, Jinping
author_sort Shen, Lazhen
collection PubMed
description 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.
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spelling pubmed-64275582019-04-15 Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release Shen, Lazhen Li, Bei Qiao, Yongsheng Song, Jinping Materials (Basel) Article 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. MDPI 2019-03-11 /pmc/articles/PMC6427558/ /pubmed/30862125 http://dx.doi.org/10.3390/ma12050828 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shen, Lazhen
Li, Bei
Qiao, Yongsheng
Song, Jinping
Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title_full Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title_fullStr Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title_full_unstemmed Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title_short Monodisperse Fe(3)O(4)/SiO(2) and Fe(3)O(4)/SiO(2)/PPy Core-Shell Composite Nanospheres for IBU Loading and Release
title_sort monodisperse fe(3)o(4)/sio(2) and fe(3)o(4)/sio(2)/ppy core-shell composite nanospheres for ibu loading and release
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427558/
https://www.ncbi.nlm.nih.gov/pubmed/30862125
http://dx.doi.org/10.3390/ma12050828
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