No abstract

Nanotechnology offers the possibility of operating on the same scale length at which biological processes occur, allowing to interfere, manipulate or study cellular events in disease or healthy conditions. The development of hybrid nanostructured materials with a high degree of chemical control and complex engineered surface including biological targeting moieties, allows to specifically bind to a single type of molecule for specific detection, signaling or inactivation processes. Magnetite nanostructures with designed composition and properties are the ones that gather most of the designs as theragnostic agents for their versatility, biocompatibility, facile production and good magnetic performance for remote in vitro and in vivo for biomedical applications. Their superparamagnetic behavior below a critical size of 30 nm has allowed the development of magnetic resonance imaging contrast agents or magnetic hyperthermia nanoprobes approved for clinical uses, establishing an inflection point in the field of magnetite based theragnostic agents.

This study presents an effective magnetic separation method for cadmium removal, based on the use of a novel nanostructured material as an adsorbent. This adsorbent involves the incorporation of magnetite nanoparticles (Fe3O4-NPs), synthesized by the reverse coprecipitation method, into sodium alginate and activated carbon to form spherical structures by crosslinking Ca2+ ions with the charged alginate chains, referred to as magnetic alginate activated carbon (MAAC) beads. The effect of the experimental parameters, such as pH, contacting time, adsorbent dosage, agitation type, and rotating speed were investigated and optimized for an efficient removal of Cd(II) ions at an initial concentration of 250 mg/L. The amount of adsorbed Cd(II) by MAAC beads increased at a pH of 6 with a removal efficiency over 90%. The maximum adsorption capacity reached was 70 mg/g of adsorbent at an initial Cd(II) concentration of 150 mg/L, whereas at 250 mg/L the adsorption capacity lowered until 60 mg/g. Sorption isotherms were calculated using Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich equations, and were better described by the Freundlich and Temkin models. These results proved the removal efficiency and the potential use under real environmental conditions of the MAAC beads, due to their easy recovery from contaminated aqueous solutions.

Challenging magnetic hyperthermia (MH) applications of immobilized magnetic nanoparticles require detailed knowledge of the effective anisotropy constant (K eff ) to maximize heat release. Designing optimal MH experiments entails the precise determination of magnetic properties, which are, however, affected by the unavoidable concurrence of magnetic interactions in common experimental conditions. In this work, a mean-field energy barrier model (𝚫E), accounting for anisotropy (E A ) and magnetic dipolar (E D ) energy, is proposed and used in combination with AC measurements to a specifically developed model system of spherical magnetic nanoparticles with well-controlled silica shells, acting as a spacer between the magnetic cores. This approach makes it possible to experimentally demonstrate the mean field dipolar interaction energy prediction with the interparticle distance, d ij , E D ≈ 1/d ij 3 and obtain the E A as the asymptotic limit for very large d ij . In doing so, K eff uncoupled from interaction contributions is obtained for the model system (iron oxide cores with average sizes of 8.1, 10.2, and 15.3 nm) revealing to be 48, 23, and 11 kJ m −3 , respectively, close to bulk magnetite/maghemite values and independent from the specific spacing shell thicknesses selected for the study.

Iron oxide magnetic nanoparticles (MNPs) have been widely studied due to their versatility for diagnosis, tracking (magnetic resonance imaging (MRI)) and therapeutic (magnetic hyperthermia and drug delivery) applications. In this work, iron oxide MNPs with different single-core (8–40 nm) and multi-core (140–200 nm) structures were synthesized and functionalized by organic and inorganic coating materials, highlighting their ability as magnetic nanotools to boost cell biotechnological procedures. Single core Fe3O4@PDA, Fe3O4@SiO2-FITC-SiO2 and Fe3O4@SiO2-RITC-SiO2 MNPs were functionalized with fluorescent components with emission at different wavelengths, 424 nm (polydopamine), 515 (fluorescein) and 583 nm (rhodamine), and their ability as transfection and imaging agents was explored with HeLa cells. Moreover, different multi-core iron oxide MNPs (Fe3O4@CS, Fe3O4@SiO2 and Fe3O4@Citrate) coated with organic (citrate and chitosan, CS) and inorganic (silica, SiO2) shells were tested as efficient nanoheaters for magnetic hyperthermia applications for mild thermal heating procedures as an alternative to simple structures based on single-core MNPs. This work highlights the multiple abilities offered by the synergy of the use of external magnetic fields applied on MNPs and their application in different biomedical approaches.