Magnetic and Plasmonic Nanoparticles for Biomedical Devices

The design of magnetic, plasmonic, and hybrid nanoparticles is a rapidly growing multidisciplinary field that has found various promising biomedical applications, including bioimaging and focused thermal cancer therapy, targeted delivery of drugs, DNA and siRNA molecules, clinical analytics and chemical and biosensing, etc. In particular, magnetic and plasmonic nanoparticles have led to an emerging trend in nanomedicine, theranostics, which combines diagnosis and therapeutic modalities in a single hybrid nanostructure..

Magnetic nanofibers for remotely triggered catalytic activity applied to the degradation of organic pollutants

This work reports on the fabrication and characterization of a novel type of electrospun magnetic nanofibers (MNFs), and their application as a magnetically-activable catalysts for degradation of organic pollutants. The magnetic stimulation capability for the catalytic action is provided by iron-manganese oxide (MnxFe2-xO4) magnetic nanoparticles (MNPs) embedded into electrospun polyacrylonitrile (PAN), which provides stability and chemical resistance. The MNPs (average size d = 40 ± 7 nm) were first obtained by a green and fast sonochemical route, and subsequently embedded into electrospun PAN nanofibers. The final MNFs showed an average diameter of 760 ± 150 nm, providing a superhydrophobic surface with contact angle (θc = 165°), as well as a considerable amount ( 50 % wt.) of embedded MNPs (Mn0.5Fe2.5O4), thermally stable up to temperatures of 330 °C. The catalytic Fe2+/3+/Mn2+/3+/4+ active centers on the MNPs of MNF’s surface could be remotely activated by alternating magnetic fields (AMF) to degrade the methyl blue (MB). Remarkable stability of the MNFs during heating under extreme pH conditions (3 80 %, after several cycles of reusing the same sample without any regeneration process. The capacity of these materials as a catalytic material with magnetic remote activation makes them appealing for those catalytic applications under conditions of darkness or restrained access, where photocatalytic reaction cannot be achieved

Evidence of the spin Seebeck effect in Ni-Zn ferrites polycrystalline slabs

We report on the observation of the spin Seebeck effect in Ni-Zn ferrites slabs with different Zn concentration. All samples have a spinel structure confirmed by XRD and TEM. We fully characterize the magnetic properties by VSM and Mössbauer spectroscopy. Samples exhibit a nonmonotonic magnetization behavior depending on the structural inversion parameter, however we found a spin Seebeck response voltage of about 25.5 nV/K independent of the magnetization and the inversion degree

The relevance of Brownian relaxation as power absorption mechanism in Magnetic Hyperthermia

The Linear Response Theory (LRT) is a widely accepted framework to analyze the power absorption of magnetic nanoparticles for magnetic fluid hyperthermia. Its validity is restricted to low applied fields and/or to highly anisotropic magnetic nanoparticles. Here, we present a systematic experimental analysis and numerical calculations of the specific power absorption for highly anisotropic cobalt ferrite (CoFe 2 O 4 ) magnetic nanoparticles with different average sizes and in different viscous media. The predominance of Brownian relaxation as the origin of the magnetic losses in these particles is established, and the changes of the Specific Power Absorption (SPA) with the viscosity of the carrier liquid are consistent with the LRT approximation. The impact of viscosity on SPA is relevant for the design of MNPs to heat the intracellular medium during in vitro and in vivo experiments. The combined numerical and experimental analyses presented here shed light on the underlying mechanisms that make highly anisotropic MNPs unsuitable for magnetic hyperthermia

Structurally oriented nano-sheets in co thin films: Changing their anisotropic physical properties by thermally-induced relaxation

We show how nanocrystalline Co films formed by separated oblique nano-sheets display anisotropy in their resistivity, magnetization process, surface nano-morphology and optical transmission. After performing a heat treatment at 270 °C, these anisotropies decrease. This loss has been monitored measuring the resistivity as a function of temperature. The resistivity measured parallel to the direction of the nano-sheets has been constant up to 270 °C, but it decreases when measured perpendicular to the nano-sheets. This suggests the existence of a structural relaxation, which produces the change of the Co nano-sheets during annealing. The changes in the nano-morphology and the local chemical composition of the films at the nanoscale after heating above 270 °C have been analysed by scanning transmission electron microscopy (STEM). Thus, an approach and coalescence of the nano-sheets have been directly visualized. The spectrum of activation energies of this structural relaxation has indicated that the coalescence of the nano-sheets has taken place between 1.2 and 1.7 eV. In addition, an increase in the size of the nano-crystals has occurred in the samples annealed at 400 °C. This study may be relevant for the application in devices working, for example, in the GHz range and to achieve the retention of the anisotropy of these films at higher temperatures

Magnetic nanoparticles for magnetically guided therapies against neural diseases

Neurological pathologies and nerve damage are two problems of significant medical and economic impact because of the hurdles of losing nerve functionality in addition to significant mortality and morbidity, and demanding rehabilitation. There are currently a number of examples of how nanotechnology can provide new solutions for biomedical problems. Current strategies for nerve repair rely on the use of functionalized scaffolds working as nerve guidance channels to improve axonal regeneration and to direct axonal re-growth across the nerve lesion site. Since low invasiveness and high selectivity of the growth stimulation are usually conflicting requirements, new approaches are being pursued in order to overcome such limitations. Engineered magnetic nanoparticles (MNPs) have emerged from this need for noninvasive therapies for both positioning and guiding neural cells in response to an external magnetic field. Here, we review the current state of the use of MNPs for neuroprotective and magnetically guided therapies. We discuss some conceivable outcomes of current magnetically driven strategies seeking integrated platforms for regenerative action on damaged tissues

Cell damage produced by magnetic fluid hyperthermia on microglial BV2 cells

We present evidence on the effects of exogenous heating by water bath (WB) and magnetic hyperthermia (MHT) on a glial micro-tumor phantom. To this, magnetic nanoparticles (MNPs) of 30-40 nm were designed to obtain particle sizes for maximum heating efficiency. The specific power absorption (SPA) values (f = 560 kHz, H = 23.9 kA/m) for as prepared colloids (533-605 W/g) dropped to 98-279 W/g in culture medium. The analysis of the intracellular MNPs distribution showed vesicle-trapped MNPs agglomerates spread along the cytoplasm, as well as large (~0.5-0.9 µm) clusters attached to the cell membrane. Immediately after WB and MHT (T = 46 °C for 30 min) the cell viability was ˜70% and, after 4.5 h, decreased to 20-25%, demonstrating that metabolic processes are involved in cell killing. The analysis of the cell structures after MHT revealed a significant damage of the cell membrane that is correlated to the location of MNPs clusters, while local cell damage were less noticeable after WB without MNPs. In spite of the similar thermal effects of WB and MHT on the cell viability, our results suggest that there is an additional mechanism of cell damage related to the presence of MNPs at the intracellular space

Quantifying the leading role of the surface state in the Kondo effect of Co/Ag(111)

Using a combination of scanning tunneling spectroscopy and atomic lateral manipulation, we obtained a systematic variation of the Kondo temperature TK of Co atoms on Ag(111) as a function of the surface-state contribution to the total density of states at the atom adsorption site ρs. By sampling the TK of a Co atom on positions where ρs was spatially resolved beforehand, we obtain a nearly linear relationship between the magnitudes. We interpret the data on the basis of an Anderson model including orbital and spin degrees of freedom [SU(4)] in good agreement with the experimental findings. The fact that the onset of the surface band is near the Fermi level is crucial to finding the observed linear behavior. In light of this model, the quantitative analysis of the experimental data evidences that at least a quarter of the coupling of Co impurities with extended states takes place through the hybridization to surface states. This result is of fundamental relevance in the understanding of Kondo screening of magnetic impurities on noble-metal surfaces, where bulk and surface electronic states coexist.Fil: Moro Lagares, M.. Biology Centre of the Academy of Sciences of the Czech Republic; República Checa. Palacky University; República Checa. Universidad de Zaragoza. Instituto de Nanociencia de Aragón; EspañaFil: Fernández, Joaquín. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; ArgentinaFil: Roura Bas, Pablo Gines. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; ArgentinaFil: Ibarra, M.R.. Universidad de Zaragoza; EspañaFil: Aligia, Armando Ángel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; ArgentinaFil: Serrate, D.. Universidad de Zaragoza; Españ

Thickness-modulated tungsten-carbon superconducting nanostructures grown by focused ion beam induced deposition for vortex pinning up to high magnetic fields

We report efficient vortex pinning in thickness-modulated tungsten–carbon-based (W–C) nanostructures grown by focused ion beam induced deposition (FIBID). By using FIBID, W–C superconducting films have been created with thickness modulation properties exhibiting periodicity from 60 to 140 nm, leading to a strong pinning potential for the vortex lattice. This produces local minima in the resistivity up to high magnetic fields (2.2 T) in a broad temperature range due to commensurability effects between the pinning potential and the vortex lattice. The results show that the combination of single-step FIBID fabrication of superconducting nanostructures with built-in artificial pinning landscapes and the small intrinsic random pinning potential of this material produces strong periodic pinning potentials, maximizing the opportunities for the investigation of fundamental aspects in vortex science under changing external stimuli (e.g., temperature, magnetic field, electrical current)

Sonochemical route for mesoporous silica-coated magnetic nanoparticles towards pH-triggered drug delivery system

This work reports a pH-triggered release system based on core@shell mesoporous magnetic nanoparticles (MNP@mSiO2) obtained using a simple and rapid ultrasound-assisted method. Performed characterization reveals magnetic cores of Fe2.9Mn0.1O4 (38 ± 6 nm) and specific loss power values adequate for hyperthermia (463 W/g), surrounded by a mesoporous silica shell (10 ± 2 nm) with large surface area (269 m2 g-1) functionalized with hydroxyl groups (-OH). MNP@mSiO2 were loaded with DOX and amino-silane grops, providing pH-triggered DOX release at acidic environments, driving by dipolar intermolecular interactions. The experimental DOX release kinetics at pH 5.5, 6.6 and 7.4 were determined and adjusted to Gompertz dissolution model (Nash–Sutcliffe efficiency coefficient (NSE>0.9)), where the only strongly pH-dependent variable is the percentage of DOX released. The pH-triggered response observed in the system was ~20% of the DOX loaded into the MNP@mSiO2 is released at pH 6.6 or 7.4, whereas up to 80 wt% is released at pH 5.5. Time to 50% of release and dissociation rate of the system remaining constant, suggesting no-pH influence on these parameters. The biological assays highlight negligible hemolytic effect and cytocompatibility of the hybrid material, pointing out the potential use of MNP@mSiO2 as a magnetic driven drug delivery system with pH-triggered drug release kinetics at acidic environments. These results probe the feasibility of sonochemical methods in the elaboration of biocompatible and controlled properties nanomaterials for drug release applications, with the advantage of accurately responses predictions by mathematical model and using minimal processing steps or laboratory equipment. © 2021 The Author