Search Results (7)

The Segura mining field, the easternmost segment of the Góis–Panasqueira–Segura tin–tungsten metallogenic belt (north–central Portugal), includes Sn-W quartz veins and Li-Sn aplite-pegmatites, which are believed to be genetically related to Variscan Granites. Sediment geochemistry indicates granite-related Ti-enrichments, locally disturbed by mineralization, suggesting magmatic and metamorphic/metasomatic titaniferous phases. Therefore, Segura alluvial samples and the geochemistry of their TiO₂ polymorphs (rutile, anatase, and brookite) were investigated, and their potential as exploration tools for Sn and W deposits was evaluated. The heavy-mineral assemblages proved to be good proxies for bedrock geology, and TiO₂ polymorph abundances were found to be suitable indicators of magmatic and/or metasomatic hydrothermal processes. The trace element geochemistry of Segura’s alluvial rutile, anatase, and brookite is highly variable, implying multiple sources and a diversity of mineral-forming processes. The main compositional differences between TiO₂ polymorphs are related to intrinsic (structural) factors, and to the P-T-X extrinsic parameters of their forming environments. Anomalous enrichments, up to 9% Nb, 6% Sn and W, 3% Fe, 2% Ta, and 1% V in rutile, and up to 1.8% Fe, 1.7% Ta, 1.2% Nb, 1.1% W 0.5% Sn and V in anatase, were registered. Brookite usually has low trace element content (<0.5%), except for Fe (~1%). HFSE-rich and granitophile-rich rutile is most likely magmatic, forming in extremely differentiated melts, with Sn and W contents enabling the discrimination between Sn-dominant and W-dominant systems. Trace element geochemical distribution maps show pronounced negative Sn (rutile+anatase) and W (rutile) anomalies linked to hydrothermal cassiterite precipitation, as opposed to their hydrothermal alteration halos and to W-dominant cassiterite-free mineralized areas, where primary hydrothermal rutile shows enrichments similar to magmatic rutile. This contribution recognizes that trace element geochemistry of alluvial TiO₂ polymorphs can be a robust, cost- and time-effective, exploration tool for Sn(W) and W(Sn) ore deposit systems. Full article

Globally, cancer is the second most common cause of death, and Europe accounts for almost 25% of the global cancer burden, although its people make up only 10% of the world’s population. Conventional systemically administered anti-cancer drugs come with important drawbacks such as inefficiency due to poor bioavailability and improper biodistribution, severe side effects associated with low therapeutic indices, and the development of multidrug resistance. Therefore, smart nano-engineered targeted drug-delivery systems with tailored pharmacokinetics and biodistribution which can selectively deliver anti-cancer agents directly to the tumor site are the solution to most difficulties encountered with conventional therapeutic tools. Here, we report on the synthesis, physicochemical characterization, and in vitro evaluation of biocompatibility and anti-tumor activity of novel magnetically targetable SPIONs based on magnetite (Fe₃O₄) nanoparticles’ surface modified with β-cyclodextrin (CD) and paclitaxel (PTX)–guest–host inclusion complexes (Fe₃O₄@β-CD/PTX). Both pristine Fe₃O₄@β-CD nanopowders and PTX-loaded thin films fabricated by MAPLE technique were investigated. Pristine Fe₃O₄@β-CD and Fe₃O₄@β-CD/PTX thin films were physicochemically characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), thermal analysis, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The biocompatibility of bare magnetic nanocomposite thin films was evaluated by MTT cell viability assay on a normal 3T3 osteoblast cell line culture and by measuring the level of NO in the culture medium. No significant modifications, neither in cell viability nor in NO level, could be observed, thereby demonstrating the excellent biocompatibility of the SPIONs thin films. Inverted phase-contrast microscopy showed no evident adverse effect on the morphology of normal osteoblasts. On the other hand, Fe₃O₄@β-CD/PTX films decreased the cell viability of the MG-63 osteosarcoma cell line by 85%, demonstrating excellent anti-tumor activity. The obtained results recommend these magnetic hybrid films as promising candidates for future delivery, and hyperthermia applications in cancer treatment. Full article

In the present work, the porous metal-organic framework (MOF) Basolite^®F300 (Fe-BTC) was tested as a potential drug-releasing depot to enhance the solubility of the anticancer drug paclitaxel (PTX) and to prepare controlled release formulations after its encapsulation in amphiphilic methoxy poly(ethylene glycol)-poly(ε-caprolactone) (mPEG-PCL) nanoparticles. Investigation revealed that drug adsorption in Fe-BTC reached approximately 40%, a relatively high level, and also led to an overall drug amorphization as confirmed by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). The dissolution rate of PTX-loaded MOF was substantially enhanced achieving a complete (100%) release within four days, while the neat drug only reached a 13% maximum rate (3–4 days). This PTX-Fe-BTC nanocomposite was further encapsulated into a mPEG-PCL matrix, a typical aliphatic amphiphilic copolyester synthesized in our lab, whose biocompatibility was validated by in vitro cytotoxicity tests toward human umbilical vein endothelial cells (HUVEC). Encapsulation was performed according to the solid-in-oil-in-water emulsion/solvent evaporation technique, resulting in nanoparticles of about 143 nm, slightly larger of those prepared without the pre-adsorption of PTX on Fe-BTC (138 nm, respectively). Transmission electron microscopy (TEM) imaging revealed that spherical nanoparticles with embedded PTX-loaded Fe-BTC nanoparticles were indeed fabricated, with sizes ranging from 80 to 150 nm. Regions of the composite Fe-BTC-PTX system in the infrared (IR) spectrum are identified as signatures of the drug-MOF interaction. The dissolution profiles of all nanoparticles showed an initial burst release, attributed to the drug amount located at the nanoparticles surface or close to it, followed by a steadily and controlled release. This is corroborated by computational analysis that reveals that PTX attaches effectively to Fe-BTC building blocks, but its relatively large size limits diffusion through crystalline regions of Fe-BTC. The dissolution behaviour can be described through a bimodal diffusivity model. The nanoparticles studied could serve as potential chemotherapeutic candidates for PTX delivery. Full article

A newly discovered tungsten ore district containing more than 300,000 tons of WO₃ in southern Anhui Province has attracted great attention. The Zhuxiling W (Mo) deposit in the district is dominated by skarn tungsten mineralization. This paper conducted in suit EPMA and LA-ICPMS spot and mapping analysis of the skarn mineral garnet to reveal the evolution of fluids, metasomatic dynamics, and formation conditions of skarn. Two generations of garnet have been identified for Zhuxiling W (Mo) skarn: 1) Gt-I generation garnet is isotropic, Al-rich grossular without zoning. As a further subdivision, Gt-IB garnet (Adr_19-46Grs_49-77 (Sps+Pyr+Alm)_4-5) contains significantly high content of Ti and Mn compared with Gt-IA garnet (Adr_3-42Grs_53-96 (Sps+Pyr+Alm)_1-5). 2) Gt-II generation garnet is anisotropic, Fe-rich andradite with oscillatory zoning. Gt-II garnet displays compositional changes with a decrease of Fe and an increase of Mn from proximal skarn (Gt-IIA) to distal skarn (Gt-IIB) with the presence of subcalcic garnet for Gt-IIB type (Sps+Pyr+Alm = 56–68). The presence of pyrrhotite associated with subcalcic garnet indicates a relatively reduced skarn system. Gt-I grossular is overall enriched in Cr, Zr, Y, Nb, and Ta compared with the Gt-II andradite, and both W and Sn strongly favor Fe-rich garnet compared with Al-rich garnet. Gt-IA grossular garnet presents a REE trend with an upward-facing parabola peaking at Pr and Nd in contrast to low and flat HREE, and Gt-IB grossular garnet has a distinct REE pattern with enriched HREE. Gt-IIA andradite garnet displays a right-dipping REE pattern (enriched LREE and depleted HREE) with a prominent positive Eu anomaly (Eu/Eu* = 3.6–15.3). In contrast, Gt-IIB andradite garnet shows depleted LREE and enriched HREE with a weak positive Eu anomaly (Eu/Eu* = 0–6.0). The incorporation and fractionation of REE in garnet are collectively controlled by crystal chemistry and extrinsic factors, such as P–T–X conditions of fluids, fluid/rock ratios, and mineral growth kinetics. Major and trace elements of two generations of garnet combined with optical and textural characteristics suggest that Gt-I Al-rich grossular garnets grow slowly through diffusive metasomatism under a closed system, whereas Gt-II Fe-rich andradite represent rapid growth garnet formed by the infiltration metasomatism of magmatic fluids in an open system. The Mn-rich garnet implies active fluid–rock interaction with Mn-rich dolomitic limestone of the Lantian Group in the district. Full article

The electronic band structures of the ordered L1₂ and L1₀ phases of the Pt_xM_1−x (M = Fe, Co and Ni) alloys were investigated using spin-polarized density functional theory (DFT). The relative contributions of both itinerant (Stoner) and localized magnetism at the high-symmetry k-points were determined and discussed qualitatively. Significant directional effects were identified along the A and R directions of the L1₀ and L1₂ alloys, respectively, and are discussed in terms of charge channeling effects. Full article

This paper presents the results of an investigation into rapidly quenched Fe-based alloys with the chemical formula: Fe₆₁Co₁₀B₂₀W₁Y_8−xPt_x (where x = 3, 4, 5). In these alloys, a small quantity of Pt was added, and the Y content was reduced concurrently. Samples of the aforementioned alloys were injection-cast in the form of plates with the dimensions: 0.5 mm × 10 mm × 10 mm. The resulting structure was examined using X-ray diffractometry (XRD), Mössbauer spectroscopy and scanning electron microscopy (SEM). The results of the structural research reveal that, with a small addition of Pt, areas rich in Pt and Y are created—in which Fe-Pt and Pt-Y compounds, with different crystallographic systems, are formed. It has also been shown that an increase in Pt content, at the expense of Y, contributed to the formation of fewer crystalline phases, i.e., it allowed a material with a more homogeneous structure to be obtained. Magnetic properties of the Fe₆₁Co₁₀B₂₀W₁Y_8−xPt_x (where x = 3, 4, 5) alloy samples were tested using a vibrating sample magnetometer (VSM). The magnetic properties of the investigated materials revealed that the saturation magnetisation increased with increasing Pt content, at the expense of Y. This effect is due to the occurrence of different proportions of crystalline magnetic phases within the volume of each alloy. Full article

Magnetic hybrid inorganic/organic nanocarriers are promising alternatives for targeted cancer treatment. The present study evaluates the preparation of manganese ferrite magnetic nanoparticles (MnFe₂O₄ MNPs) encapsulated within Paclitaxel (PTX) loaded thioether-containing ω-hydroxyacid-co-poly(d,l-lactic acid) (TEHA-co-PDLLA) polymeric nanoparticles, for the combined hyperthermia and chemotherapy treatment of cancer. Initially, TEHA-co-PDLLA semitelechelic block copolymers were synthesized and characterized by ¹H-NMR, FTIR, DSC, and XRD. FTIR analysis showed the formation of an ester bond between the two compounds, while DSC and XRD analysis showed that the prepared copolymers were amorphous. MnFe₂O₄ MNPs of relatively small crystallite size (12 nm) and moderate saturation magnetization (64 emu·g⁻¹) were solvothermally synthesized in the sole presence of octadecylamine (ODA). PTX was amorphously dispersed within the polymeric matrix using emulsification/solvent evaporation method. Scanning electron microscopy along with energy-dispersive X-ray spectroscopy and transmission electron microscopy showed that the MnFe₂O₄ nanoparticles were effectively encapsulated within the drug-loaded polymeric nanoparticles. Dynamic light scattering measurements showed that the prepared nanoparticles had an average particle size of less than 160 nm with satisfactory yield and encapsulation efficiency. Diphasic PTX in vitro release over 18 days was observed while PTX dissolution rate was mainly controlled by the TEHA content. Finally, hyperthermia measurements and cytotoxicity studies were performed to evaluate the magnetic response, as well as the anticancer activity and the biocompatibility of the prepared nanocarriers. Full article