Magnetic hyperthermia (MHT) exploits magnetic nanoparticles (MNPs) to burn solid tumors. Here, we overview promising MNPs and magnetic assemblies used in MHT alone or in combination with chemotherapy, radiotherapy, immunotherapy or phototherapy.
The assembly of magnetic cores into regular structures may notably influence the properties displayed by a magnetic colloid. Here, key synthesis parameters driving the self‐assembly process capable of organizing colloidal magnetic cores into highly regular and reproducible multi‐core nanoparticles are determined. In addition, a self‐consistent picture that explains the collective magnetic properties exhibited by these complex assemblies is achieved through structural, colloidal, and magnetic means. For this purpose, different strategies to obtain flower‐shaped iron oxide assemblies in the size range 25–100 nm are examined. The routes are based on the partial oxidation of Fe(OH)2, polyol‐mediated synthesis or the reduction of iron acetylacetonate. The nanoparticles are functionalized either with dextran, citric acid, or alternatively embedded in polystyrene and their long‐term stability is assessed. The core size is measured, calculated, and modeled using both structural and magnetic means, while the Debye model and multi‐core extended model are used to study interparticle interactions. This is the first step toward standardized protocols of synthesis and characterization of flower‐shaped nanoparticles.
Magnetic nanoparticles are being
developed as structural and functional
materials for use in diverse areas, including biomedical applications.
Here, we report the synthesis of maghemite (γ-Fe
2
O
3
) nanoparticles with distinct morphologies: single-core
and multicore, including hollow spheres and nanoflowers, prepared
by the polyol process. We have used sodium acetate to control the
nucleation and assembly process to obtain the different particle morphologies.
Moreover, from samples obtained at different time steps during the
synthesis, we have elucidated the formation mechanism of the nanoflowers:
the initial phases of the reaction present a lepidocrocite (γ-FeOOH)
structure, which suffers a fast dehydroxylation, transforming to an
intermediate “undescribed” phase, possibly a partly
dehydroxylated lepidocrocite, which after some incubation time evolves
to maghemite nanoflowers. Once the nanoflowers have been formed, a
crystallization process takes place, where the γ-Fe
2
O
3
crystallites within the nanoflowers grow in size (from
∼11 to 23 nm), but the particle size of the flower remains
essentially unchanged (∼60 nm). Samples with different morphologies
were coated with citric acid and their heating capacity in an alternating
magnetic field was evaluated. We observe that nanoflowers with large
cores (23 nm, controlled by annealing) densely packed (tuned by low
NaAc concentration) offer 5 times enhanced heating capacity compared
to that of the nanoflowers with smaller core sizes (15 nm), 4 times
enhanced heating effect compared to that of the hollow spheres, and
1.5 times enhanced heating effect compared to that of single-core
nanoparticles (36 nm) used in this work.
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