Raman spectroscopy is a very valuable and fast-performance tool to gain insight first into the different iron oxide phases present in nanoparticles, to correlate then the magnetic properties with potential bio-related applications.
The large magnetophoretic mobility stemming from the large magnetic susceptibility and the very small coercivity of octapod-shaped iron oxide nanoparticles improve their capability for magnetic separation.
Currently, the nanoparticle functionalization effect on supramolecular peptide-based hydrogels remains undescribed, but is expected to affect the hydrogels’ self-assembly and final magnetic gel properties. Herein, two different functionalized nanoparticles: citrate-stabilized (14.4 ± 2.6 nm) and lipid-coated (8.9 ± 2.1 nm) magnetic nanoparticles, were used for the formation of dehydropeptide-based supramolecular magnetogels consisting of the ultra-short hydrogelator Cbz-L-Met-Z-ΔPhe-OH, with an assessment of their effect over gel properties. The lipid-coated nanoparticles were distributed along the hydrogel fibers, while citrate-stabilized nanoparticles were aggregated upon gelation, which resulted into a heating efficiency improvement and decrease, respectively. Further, the lipid-coated nanoparticles did not affect drug encapsulation and displayed improved drug release reproducibility compared to citrate-stabilized nanoparticles, despite the latter attaining a stronger AMF-trigger. This report points out that adsorption of nanoparticles to hydrogel fibers, which display domains that improve or do not affect drug encapsulation, can be explored as a means to optimize the development of supramolecular magnetogels to advance theranostic applications.
Antiphase boundaries perpendicular to the [111] direction of the spinel structure of the nanocrystals promote a local Fe–Fe enrichment at these individual lattice defects.
The bioaccumulation of polycyclic aromatic compounds originating from textile processing industries is nowadays a major environmental problem worldwide. In order to tackle this situation, several inorganic semiconductors have been tested as photocatalysts for the degradation of these harmful pollutants in the search of sustainable and cost-effective solutions. Nevertheless, these semiconductor materials often involve important limitations such as poor efficiency and selectivity, which in the end substantially restrict their implementation at the industrial scale. As an alternative, we herein report the fabrication and application of Au-decorated titanate nanotubes (TNTs) as high-performance architectures for the selective degradation of organic contaminants. This synthetic strategy is intended to establish a synergetic integration of the physicochemical and photocatalytic features of these hybrid nanostructures by combining the remarkable adsorption capabilities of TNTs with the enhanced light-harvesting efficiency provided by the incorporation of a noble metal component. The obtained results evidence the great potential that rationally designed plasmonic composites may have for the development of selective environmental remediation technologies and in particular on the current challenges faced by the wastewater treatment sector.
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