Cargando…

Facile transformation of FeO/Fe(3)O(4) core-shell nanocubes to Fe(3)O(4) via magnetic stimulation

Here, we propose the use of magnetic hyperthermia as a means to trigger the oxidation of Fe(1−x)O/Fe(3−δ)O(4) core-shell nanocubes to Fe(3−δ)O(4) phase. As a first relevant consequence, the specific absorption rate (SAR) of the initial core-shell nanocubes doubles after exposure to 25 cycles of alte...

Descripción completa

Detalles Bibliográficos
Autores principales: Lak, Aidin, Niculaes, Dina, Anyfantis, George C., Bertoni, Giovanni, Barthel, Markus J., Marras, Sergio, Cassani, Marco, Nitti, Simone, Athanassiou, Athanassia, Giannini, Cinzia, Pellegrino, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036086/
https://www.ncbi.nlm.nih.gov/pubmed/27665698
http://dx.doi.org/10.1038/srep33295
Descripción
Sumario:Here, we propose the use of magnetic hyperthermia as a means to trigger the oxidation of Fe(1−x)O/Fe(3−δ)O(4) core-shell nanocubes to Fe(3−δ)O(4) phase. As a first relevant consequence, the specific absorption rate (SAR) of the initial core-shell nanocubes doubles after exposure to 25 cycles of alternating magnetic field stimulation. The improved SAR value was attributed to a gradual transformation of the Fe(1−x)O core to Fe(3−δ)O(4), as evidenced by structural analysis including high resolution electron microscopy and Rietveld analysis of X-ray diffraction patterns. The magnetically oxidized nanocubes, having large and coherent Fe(3−δ)O(4) domains, reveal high saturation magnetization and behave superparamagnetically at room temperature. In comparison, the treatment of the same starting core-shell nanocubes by commonly used thermal annealing process renders a transformation to γ-Fe(2)O(3). In contrast to other thermal annealing processes, the method here presented has the advantage of promoting the oxidation at a macroscopic temperature below 37 °C. Using this soft oxidation process, we demonstrate that biotin-functionalized core-shell nanocubes can undergo a mild self-oxidation transformation without losing their functional molecular binding activity.