Synthesis and magnetic behavior of ultra-small bimetallic FeCo/graphite nanoparticles.

FeCo-alloy graphite-coated nanoparticles with mean particle diameter under 8 nm have been synthesized following a CVD carbon-deficient method. The superior magnetic properties of FeCo-alloy nanoparticles makes them good candidates to be used as magnetic filler in magneto-polymer composites. Thanks to the protective effect of the graphite shell, FeCo nanoparticles are stable under oxygen atmosphere up to 200 ° C. The as-prepared nanoparticles presented a highly long range chemically ordered core being ferromagnetic at room temperature with a saturation magnetization at room temperature close to the bulk value. After annealing at 750 K the saturation magnetization and the coercive field increase. To investigate the processes involved in the thermal treatment, the temperature dependence of the magnetization and the particle composition, size and structure have been characterized before and after annealing. Besides powder x-ray diffraction (XRD) and x-ray photoelectron spectroscopy (XPS), a detailed study by means of advanced transmission electron microscopy (TEM) techniques has been carried out. In particular, aberration corrected scanning transmission electron microscopy (STEM), has shown that nanoparticles became faceted after the thermal treatment, as a mechanism to reach the thermodynamic equilibrium within the metastable phase. This outstanding feature, not previously reported, leads to an increase of the shape anisotropy, which in turn might be the origin of the observed increase of the coercive field after annealing.

Synthesis and characterization of ultra-small magnetic FeNi/G and NiCo/G nanoparticles.

Ultra-small magnetic nanoparticles consisting of NiCo and FeNi alloys enclosed within graphitic shells (NiCo/G and FeNi/G) have been synthesized. The particles, which retained the face centered cubic (fcc) symmetry of the original bulk metals, together with the graphitic coating were characterized by means of aberration corrected scanning transmission electron microscopy (STEM), obtaining mean particle sizes of 2.6 nm and 6.2 nm for NiCo/G and FeNi/G, respectively. Due to the enhancement of the thermal stability by the graphite shell, the graphite coated FeNi and NiCo were stable under oxygen atmosphere up to 170 °C. The effectiveness of the graphite shell was confirmed when unprotected bimetallic FeNi and NiCo were prepared and chemical characterization revealed that more than 60 at.% of the samples was oxygen due to the massive oxidation of the bimetallic nanoparticles.

Use of a polyol liquid collection medium to obtain ultrasmall magnetic nanoparticles by laser pyrolysis.

The present work addresses the main bottleneck in the synthesis of magnetic nanoparticles by laser pyrolysis. Since the introduction of laser pyrolysis for the production of nanoparticles nearly three decades ago, this method has been repeatedly presented as a highly promising alternative, on account of two main characteristics: (i) its flexibility, since nanoparticles can be formed from a wide variety of precursors in both gas and liquid phase, and (ii) its continuous nature, avoiding the intrinsic variability of batch processing. However, the results reported to date invariably show considerable aggregation of the obtained nanoparticles, which strongly limits their application in most fields. In this work, we have been able to circumvent this problem by collecting the particles in a polyol liquid medium. This method prevents the formation of aggregates and renders a uniform distribution of well dispersed ultrasmall nanoparticles (<4 nm) in a water-compatible solvent. We consider that the effectiveness of this novel collection method for the production of well-dispersed magnetic nanoparticles will be of high interest to a wide range of scientists working in the nanoparticle synthesis field and may enable new applications wherever there is a strict requirement for non-agglomerated nanoparticles.

Chitosan derivatives as nanocarriers for hLDHA inhibitors delivery to hepatic cells: A selective strategy for targeting primary hyperoxaluria diseases.

Primary hyperoxalurias (PHs) are a group of inherited alterations of the hepatic glyoxylate metabolism that result in an excess of oxalate production by the oxidation of glyoxylate by the human lactate dehydrogenase A enzyme (hLDHA). The selective liver inhibition of this enzyme is one of the therapeutic strategies followed in the treatment of this disease. Even though several efforts have been recently performed using gene silencing by the RNA interference approach, small-molecule inhibitors that selectively reach hepatocytes are preferred since they present the advantages of a lower production cost and better pharmacological properties. In that sense, the design, synthesis, and physicochemical characterization by NMR, FTIR, DLS and TEM of two nanocarriers based on chitosan conjugates (1, non-redox-sensitive; 2, redox-sensitive) have been performed to (i) achieve the selective transport of hLDHA inhibitors into hepatocytes and (ii) their disruption once they reach the hepatocytes cytosol. Polymer 2 self-assembled into micelles in water and showed high drug loadings (19.8-24.5 %) and encapsulation efficiencies (31.9-40.8%) for the hLDHA inhibitors (I-III) tested. The non-redox-sensitive micelle 1 remained stable under different glutathione (GSH) concentrations (10 µM and 10 mM), and just a residual release of the inhibitor encapsulated was observed (less than 10 %). On the other hand, micelle 2 was sufficiently stable under in vitro physiological conditions (10 µM, GSH) but it quickly disassembled under the simulated reducing conditions present inside hepatocytes (10 mM GSH), achieving a 60 % release of the hLDHA inhibitor encapsulated after 24 h, confirming the responsiveness of the developed carrier to the high levels of intracellular GSH.

Enhancement of the fatigue life of recycled PP by incorporation of recycled opaque PET collected from household milk bottle wastes.

Opaque PET (Polyethylene terephthalate) was recently introduced as a dairy packaging, mainly for milk bottles. Opaque PET, obtained as PET filled with mineral nanoparticles, allows for a reduction of bottles' thickness, thus a cost reduction for industrials. For this reason, the use of opaque PET is steadily increasing. However, its recyclability is nowadays an issue: although the recycling channels are well established for transparent PET, the presence of opaque PET in the household wastes weakens the existing recycling channels. Besides, many initiatives are launched in Europe to turn wastes into resources, as one key to a more circular economy. One of the biggest challenges is an efficient sorting of the plastic solid wastes since the PET is not miscible with other plastics such as polypropylene (PP) from the bottle caps and polyethylene (PE) from the other milk bottles. In this work, the mechanical properties of uncompatibilized blends of opaque PET (rPET-O) with recycled polypropylene (rPP) have been studied; both are collected from household wastes. The tensile properties and the fatigue life of rPP, monitored by in-situ digital image correlation and in-situ infrared thermography, are increased by the incorporation of rPET-O. rPET-O/rPP blends may be substituted to rPP for similar applications, with no need to sort the caps from the bottles. Thus, as a concept, the incorporation of opaque PET into the PP recycling sector may be a new route to absorb some of the growing amounts of opaque PET.

A unique multidrug nanomedicine made of squalenoyl-gemcitabine and alkyl-lysophospholipid edelfosine.

Among anticancer nanomedicines, squalenoyl nanocomposites have obtained encouraging outcomes in a great variety of tumors. The prodrug squalenoyl-gemcitabine has been chosen in this study to construct a novel multidrug nanosystem in combination with edelfosine, an alkyl-lysophopholipid with proven anticancer activity. Given their amphiphilic nature, it was hypothesized that both anticancer compounds, with complementary molecular targets, could lead to the formation of a new multitherapy nanomedicine. Nanoassemblies were formulated by the nanoprecipitation method and characterized by dynamic light scattering, transmission electron microscopy and X-ray photoelectron spectroscopy. Because free edelfosine is highly hemolytic, hemolysis experiments were performed using human blood erythrocytes and nanoassemblies efficacy was evaluated in a patient-derived metastatic pediatric osteosarcoma cell line. It was observed that these molecules spontaneously self-assembled as stable and monodisperse nanoassemblies of 51 ±â€¯1 nm in a surfactant/polymer free-aqueous suspension. Compared to squalenoyl-gemcitabine nanoassemblies, the combination of squalenoyl-gemcitabine with edelfosine resulted in smaller particle size and a new supramolecular conformation, with higher stability and drug content, and ameliorated antitumor profile.