Nanoscale engineering of hybrid magnetite–carbon nanofibre materials for magnetic resonance imaging contrast agents

Magnetic nanomaterials show significant promise as contrast agents for magnetic resonance imaging (MRI). We have developed a new highly efficient one-step procedure for the synthesis of magnetically- functionalised hollow carbon nanofibres, where (i) the carbon nanofibres act as both a template and a support for the nucleation and growth of magnetite nanoparticles and (ii) the structural (size, dispersity and morphology) and functional (magnetisation and coercivity) properties of the magnetic nanoparticles formed on nanofibres are strictly controlled by the mass ratio of the magnetite precursor to the nanofibres and the solvent employed during synthesis. We have shown that our magnetite-nanofibre materials are effectively solubilised in water resulting in a stable suspension that has been employed as a ‘‘negative’’ MRI contrast agent with an excellent transverse relaxivity (r2) of (268 13) mM s 1, surpassing current commercial materials and state-of-the-art magnetic nanoscale platforms in performance for MRI contrast at high magnetic fields. The preparation and evaluation of this unique hybrid nanomaterial represents a critical step towards the realisation of a highly efficient ‘‘smart’’ MRI theranostic agent – a material that allows for the combined diagnosis (with MRI), treatment (with magnetic targeting) and follow-up of a disease (with MRI) – currently in high demand for various clinical applications, including stratified nanomedicine

The Structure and Magnetic Properties of Sm₂Fe₁₇C<em>_x</em> Compounds Prepared from Ball-Milled Mixtures of Sm₂Fe₁₇ and Carbon Nanotubes or Graphite

The processing route of Sm2Fe17 carbides is shorter than that of nitrides, which can potentially be used for cost-effective mid-performance magnets’ production. The magnetic properties of Sm2Fe17Cx compounds can be controlled at the annealing step, which allows them to be used for a variety of applications. In this work, X-ray diffraction (XRD) analysis, Mössbauer spectroscopy, scanning and transmission electron microscopy (SEM, TEM) and vibrating sample magnetometry (VSM) were used for characterization of the structure and magnetic properties of Sm2Fe17Cx compounds. The powder samples were prepared by high-energy ball milling of Sm2Fe17 mixtures with carbon nanotubes (CNT) or graphite with subsequent annealing. The formation of Sm2Fe17Cx compounds after annealing was followed by the formation of α-Fe and amorphous Sm2O3. The hyperfine field values of Fe atoms of all the Sm2Fe17 lattice sites increased by 12% on average after annealing that was caused by carbon diffusion. The coercivity of the samples peaked after annealing at 375 °C. The samples with CNT demonstrated an increase of up to 14% in coercivity and 5% in specific remanence in the range of 250–375 °C annealing temperatures

Structure and Magnetic Properties of SrFe12&minus;xInxO19 Compounds for Magnetic Hyperthermia Applications

In this work, complex studies of the structure and magnetic properties of SrFe12&minus;xInxO19 powders obtained by the mechanochemical and citrate methods were carried out. The solubility of In in strontium hexaferrite SrFe&#8321;&#8322;O&#8321;&#8329; at 1200 &deg;C was determined. The structure and properties of the powders were studied using X-ray diffraction analysis, M&ouml;ssbauer spectroscopy and scanning electron microscopy. Measurements of magnetic properties in magnetic fields up to 1600 kA/m were also performed. Additionally, the hyperthermia effect was investigated. The possibility of controlling the coercivity of the samples in the range from 188.9 kA/m to 22.3 kA/m and saturation magnetization from 63.5 A&middot;m2/kg to 44.2 A&middot;m2/kg with an increase in the degree of In doping was also demonstrated. Investigation of the magnetic hyperthermia of the samples was carried out by temperature measurement with an IR camera when they were introduced into alternating magnetic fields of various frequencies (144, 261 and 508 kHz) and amplitudes (between 11.96 and 19.94 kA/m). According to the study result, there was detected the heating of the SrFe12&minus;xInxO19 sample (x = 1.7). The highest values of magnetic hyperthermia of the sample were observed in a 19.94 kA/m magnetic field and a frequency of 261 kHz. At a concentration of 56.67 g/L, the sample was heated from 23 to 41 &deg;C within 2 min. The parameters SLP (specific loss power) and ILP (intrinsic loss power) were calculated

Impact of Ag on the Limit of Detection towards NH3-Sensing in Spray-Coated WO3 Thin-Films

Ag-doped WO3 (Ag&ndash;WO3) films were deposited on a soda-lime glass substrate via a facile spray pyrolysis technique. The surface roughness of the films varied between 0.6 nm and 4.3 nm, as verified by the Atomic Force Microscopy (AFM) studies. Ammonia (NH3)-sensing measurements of the films were performed for various concentrations at an optimum sensor working temperature of 200 &deg;C. Enrichment of oxygen vacancies confirmed by X-ray Photoelectron Spectroscopy (XPS) in 1% Ag&ndash;WO3 enhanced the sensor response from 1.06 to 3.29, approximately 3 times higher than that of undoped WO3. Limit of detection (LOD) up to 500 ppb is achieved for 1% Ag&ndash;WO3, substantiating the role of Ag in improving sensor performance

Structural synergy of NanoAl2O3/NanoAl composites with high thermomechanical properties and ductility

Achieving a combination of high strength and ductility in metal-based composites is still a difficult task, and it is especially challenging in a wide temperature range. Here, nanoAl2O3/nanoAl composites with high tensile and compressive strength and excellent ductility at 25 and 500 °C were obtained using Al and Al2O3 nanopowders via a combination of high-energy ball milling (HEBM) and spark plasma sintering (SPS). Being about three times lighter than conventional high-strength steel (with a density of 2.7 g/cm3 vs. that of 7.8 g/cm3 for steel), the nanoAl2O3/nanoAl materials demonstrated tensile strength and elongation before failure comparable with those of steel. The nanoAl2O3/nanoAl composites were strengthened with two types of Al2O3 NPs, in situ formed, and introduced into the powder mixture. The resulting materials had a bimodal microstructure consisting of Al with micron and submicron grains surrounded by an Al/Al2O3 framework whose structural components were all in the size range of 20–50 nm. Among the studied compositions (0, 1, 2, 3, 4, 5, 10, and 20 wt.% of Al2O3), the Al-3%Al2O3 material showed the best thermomechanical properties, such as a tensile strength of 512 MPa and 280 MPa and a compressive strength of 489 MPa and 344 MPa at 25 and 500 °C, respectively, with an elongation to failure of 15–18%. These results show the promise of nanoAl2O3/nanoAl composites for use as small items in the automotive and aviation industries.</p

Physical Vapor Deposition Features of Ultrathin Nanocrystals of Bi2(TexSe1- x)3

Structural and electronic properties of ultrathin nanocrystals of chalcogenide Bi2(TexSe1-x)3were studied. The nanocrystals were formed from the parent compound Bi2Te2Se on as-grown and thermally oxidized Si(100) substrates using Ar-assisted physical vapor deposition, resulting in well-faceted single crystals several quintuple layers thick and a few hundreds nanometers large. The chemical composition and structure of the nanocrystals were analyzed by energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, electron backscattering, and X-ray diffraction. The electron transport through nanocrystals connected to superconducting Nb electrodes demonstrated Josephson behavior, with the predominance of the topological channels [ Stolyarov et al. Commun. Mater., 2020, 1, 38 ]. The present paper focuses on the effect of the growth conditions on the morphology, structural, and electronic properties of nanocrystals

Study of Cytotoxicity and Internalization of Redox-Responsive Iron Oxide Nanoparticles on PC-3 and 4T1 Cancer Cell Lines

Redox-responsive and magnetic nanomaterials are widely used in tumor treatment separately, and while the application of their combined functionalities is perspective, exactly how such synergistic effects can be implemented is still unclear. This report investigates the internalization dynamics of magnetic redox-responsive nanoparticles (MNP-SS) and their cytotoxicity toward PC-3 and 4T1 cell lines. It is shown that MNP-SS synthesized by covalent grafting of polyethylene glycol (PEG) on the magnetic nanoparticle (MNP) surface via SS-bonds lose their colloidal stability and aggregate fully in a solution containing DTT, and partially in conditioned media, whereas the PEGylated MNP (MNP-PEG) without S-S linker control remains stable under the same conditions. Internalized MNP-SS lose the PEG shell more quickly, causing enhanced magnetic core dissolution and thus increased toxicity. This was confirmed by fluorescence microscopy using MNP-SS dual-labeled by Cy3 via labile disulfide, and Cy5 via a rigid linker. The dyes demonstrated a significant difference in fluorescence dynamics and intensity. Additionally, MNP-SS demonstrate quicker cellular uptake compared to MNP-PEG, as confirmed by TEM analysis. The combination of disulfide bonds, leading to faster dissolution of the iron oxide core, and the high-oxidative potential Fe3+ ions can synergically enhance oxidative stress in comparison with more stable coating without SS-bonds in the case of MNP-PEG. It decreases the cancer cell viability, especially for the 4T1, which is known for being sensitive to ferroptosis-triggering factors. In this work, we have shown the effect of redox-responsive grafting of the MNP surface as a key factor affecting MNP-internalization rate and dissolution with the release of iron ions inside cancer cells. This kind of synergistic effect is described for the first time and can be used not only in combination with drug delivery, but also in treatment of tumors responsive to ferroptosis

Features of the Phase Preferences, Long- and Short-Range Order in <i>Ln</i>₂(WO₄)₃ (<i>Ln</i> = Gd, Dy, Ho, Yb) with Their Relation to Hydration Behavior

The effect of synthesis conditions on the features of the long- and short-range order of Ln2(WO4)3 (Ln = Gd, Dy, Ho, Yb) powders synthesized via coprecipitation of salts has been studied by a complex of physico-chemical techniques including synchrotron X-ray powder diffraction, X-ray absorption spectroscopy, Raman and infrared spectroscopy, and simultaneous thermal analysis. It was found that crystallization of amorphous precursors begins at 600 °C/3 h and leads to the formation of the monoclinic structure with sp. gr. C12/c1(15) for Ln2(WO4)3 (Ln = Gd, Dy) and with sp. gr. P121/a1(14) for Ln = Yb, whereas crystallization of Ho precursor requires even higher temperature. After annealing at 1000 °C, the P121/a1(14) phase becomes the dominant phase component for all heavy lanthanoid types except for Ln = Gd. It was shown that the Ln (Ln = Dy, Ho, and Yb) tungstates with the P121/a1(14) monoclinic structure correspond to trihydrates Ln2(WO4)3·3H2O formed due to a rapid spontaneous hydration under ambient conditions. It was concluded that the proneness to hydration is due to a specific structure of the P121/a1(14) phase with large voids available to water molecules. Modifications in the local structure of Ln-O coordination shell accompanying the structure type change and hydration are monitored using EXAFS spectroscopy