Search Results (85)

Due to their excellent physicochemical properties, the nanoparticles (NPs) have been utilized in various potential applications, including environmental remediation, energy storage, and nanomedicine. In this work, the ultrasonic and manual stirring approaches were used to integrate yttrium oxide (Y₂O₃) nanoparticles (NPs) into reduced graphene oxide (RGO) and carbon nanotubes (CNTs) to enhance their photocatalytic and anticancer properties. Pure Y₂O₃NPs, Y₂O₃/RGO NCs, and Y₂O₃/CNTs NCs were characterized using different analytical techniques, such as XRD, SEM, EDX with Elemental Mapping, FTIR, UV-Vis, PL, and DLS to investigate their improved structural, surface morphological, chemical bonding, optical, and surface charge properties. XRD data confirmed the successful integration of Y₂O₃into RGO and CNTs, with minor changes in crystallite sizes. SEM images with EDX analysis revealed that Y₂O₃NPs were uniformly distributed on RGO and CNTs, reducing aggregation. Chemical bonding and interactions between Y₂O₃and carbon materials were investigated using Fourier Transform Infrared (FTIR) analysis. UV and PL results suggest that the optical studies showed a shift in absorption peaks upon integration with RGO and CNTs. This indicates enhanced light absorption and modifications to the band gap between (3.79–4.40 eV) for the obtained samples. In the photocatalytic experiment, the degradation efficiency of bromophenol blue (BPB) dye for Y₂O₃RGO NCs was up to 87.3%, outperforming pure Y₂O₃NPs (45.83%) and Y₂O₃/CNTs NCs (66.78%) after 120 min of UV irradiation. Additionally, the MTT assay demonstrated that Y₂O₃/RGO NCs exhibited the highest anticancer activity against MG-63 bone cancer cells with an IC50 value of 45.7 µg/mL compared to Y₂O₃CNTs NCs and pure Y₂O₃NPs. This work highlights that Y₂O₃/RGO NCs could be used in significant applications, including environmental remediation and in vivo cancer therapy studies. Full article

Eukaryotic cells respond to oxidative stress (OS), a physiological condition characterized by the accumulation of reactive oxygen species (ROS), through various protective mechanisms. The antioxidant defense system (ADS) is activated either by post-translational modifications of pre-existing proteins or through the induction of gene expression. These mechanisms protect cellular biomolecules against ROS damage. Although extensive research has been conducted in different species, there is limited information regarding the specific response of Yarrowia lipolytica to OS. This study aims to elucidate the molecular mechanisms by which Y. lipolytica responds to OS by analyzing the expression of genes encoding enzymes involved in antioxidant response, such as superoxide dismutase (Sod), catalase (Cat), and glutathione peroxidase (Gpx). The Y. lipolytica genome contains three CAT genes, one SOD gene, one copper chaperone for Sod (CCS) gene, and one GPX gene. The expression profiles of these genes were assessed in Y. lipolytica cells exposed to H₂O₂ [5 mM] over time. All genes reached their maximal expression within the first 15 min of exposure. Comparative analysis between young and aged Y. lipolytica cells subjected to OS revealed that young cells exhibited higher expression levels for all genes, with CAT3 and SOD showing the highest expression values. These findings suggest that the enzymes encoded by these genes play a crucial role in the antioxidant response of this species. To our knowledge, this is the first study demonstrating that the ADS in Y. lipolytica is regulated at the transcriptional level. Full article

Objective: Yttria-stabilized tetragonal zirconia polycrystal (Y-TZP), a variant of zirconia (ZrO₂), has attracted interest as a substitute for titanium in dental and orthopedic implants, valued for its biocompatibility and aesthetics that resemble natural teeth. However, its bioinert surface limits osseointegration, making surface modifications such as calcium phosphate (CaP) coatings highly relevant. Materials and methods: The review process adhered to the PRISMA guidelines. Electronic searches of PubMed, Scopus, Web of Science, Embase, and Cochrane Library (July 2025) identified studies evaluating CaP-coated zirconia implants. Eligible studies included in vitro, in vivo, and preclinical investigations with a control group. Data on coating type, deposition method, and biological outcomes were extracted and analyzed. Results: A total of 27 studies were analyzed, featuring different calcium phosphate (CaP) coatings including β-tricalcium phosphate (β-TCP), hydroxyapatite (HA), octacalcium phosphate (OCP), and various composites. These coatings were applied using diverse techniques such as RF magnetron sputtering, sol–gel processing, biomimetic methods, and laser-based approaches. In multiple investigations, calcium phosphate coatings enhanced osteoblast attachment, proliferation, alkaline phosphatase (ALP) expression, and bone-to-implant contact (BIC) relative to unmodified zirconia surfaces. Multifunctional coatings incorporating growth factors, antibiotics, or nanoparticles showed additional benefits. Conclusion: CaP coatings enhance the bioactivity of zirconia implants and represent a promising strategy to overcome their inertness. Further standardized approaches and long-term studies are essential to verify their translational relevance. Full article

Background/Objectives: The growing prevalence of metabolic-associated steatotic liver disease (MASLD)/metabolic-associated steatohepatitis (MASH) is forecasted to be over 55% by 2040, representing a significant driver of cirrhosis and highlighting demand for effective therapeutic interventions. The therapeutic landscape is evolving with agents, like glucagon-like peptide-1 receptor agonists (GLP-1 RAs), under active investigation. A common concern across emerging therapies is potentially precipitating decompensation in patients with existing cirrhosis, necessitating careful consideration in this population. Case Presentation: A 46 y.o. female with obesity and cirrhosis from MASH and alcohol who underwent a deceased-donor liver transplant developed steatohepatitis within a year post-transplant after gaining 36 kg. Transient elastography revealed controlled attenuation parameter (CAP) 400 dB/m (S3 steatosis) and liver stiffness measurement (LSM) 61.2 kPa (advanced fibrosis). Follow-up biopsy confirmed severe steatohepatitis (NAS 7/8) and advanced fibrosis (F3), attributed to metabolic dysfunction without evidence of alcohol recurrence. She decompensated with ascites and varices, leading to transplant re-enlistment at MELD-Na 29. Despite two years of intensive lifestyle modification, losing 17 kg, and recompensation, her follow-up elastography showed persistent steatosis (S3) and advanced fibrosis (F4). Subsequent allograft biopsy revealed progression to cirrhosis (F4) with ongoing steatohepatitis (NAS 3/8). Tirzepatide was initiated for the development of type 2 diabetes, attributed to steroids used for immunosuppression. After 2 years on tirzepatide, she lost 43.1 kg. Shockingly, her follow-up elastography demonstrated fibrosis regression with LSM 5.5 kPa (F1) and steatohepatitis resolution with CAP 204 dB/m (S0). Follow-up liver biopsy confirmed fibrosis regression to F2-F3 and steatohepatitis resolution (NAS 1/8). Conclusions: This case challenges the widely accepted dogma that liver MASH cirrhosis is irreversible. Using multiple liver fibrosis monitoring modalities, cirrhosis reversal was demonstrated and attributed to mechanisms of GLP-1/GIP RA therapy. This study suggests that GLP-1/GIP RA may be safe in cirrhosis and may result in fibrosis regression. Full article

This article deals with the effect of Kr¹⁵⁺ ion irradiation on the structure and properties of partially stabilized zirconium dioxide (ZrO₂ + 3 mol. % Y₂O₃) ceramics. Ion irradiation is used to simulate radiation damage typical of operating conditions in nuclear reactors and space technology. It is shown that with an increase in the irradiation fluence, point defects are formed, dislocations accumulate, and the crystal lattice parameters change. At high fluences (>10¹³ ions/cm²), a phase transition of the monoclinic (m-ZrO₂) phase to the tetragonal (t-ZrO₂) and cubic (c-ZrO₂) modifications is observed, which is accompanied by a decrease in the crystallite size and an increase in internal stresses. Changes in the mechanical properties of the material were also observed: at moderate irradiation fluences, strengthening is observed due to the formation of dislocation structures, whereas at high fluences (>10¹⁴ ions/cm²), a decrease in strength and a potential amorphization of the structure begins. The change in the phase composition was confirmed by X-ray phase analysis and Raman spectroscopy. The results obtained allow a deeper understanding of the mechanisms of radiation-induced phase transformations in stabilized ZrO₂ and can be used in the development of ceramic materials with increased radiation resistance. Full article

Protein functional effector (pfe)RNAs were introduced in 2015 as PIWI-interacting-like small noncoding (nc)RNAs and were later categorized as a novel group based on being 2′-O-methylated at their 3′-end, directly binding and affecting protein function, but not levels, and not matching known RNAs. Here, we document that human pfeRNAs match fragments of GenBank database-annotated human ncRNAs. PDLpfeRNAa matches the 3′-half fragment of a mitochondrial transfer (t)RNA, and PDLpfeRNAb matches a 28S ribosomal (r)RNA fragment. These PDLpfeRNAs are known to bind to tumor programmed death ligand (PD-L)1, enhancing or inhibiting its interaction with lymphocyte PD-1 and consequently tumor immune escape, respectively. In a validated 8-pfeRNA-set classifier for pulmonary nodule presence and benign vs. malignant nature, seven here match one or more of the following: transfer, micro, Y, PIWI, long (lnc)RNAs, and a PDLpfeRNAa fragment. The previously identified chromosomal locations of these pfeRNAs and their matches partially overlap. Another 2-pfeRNA set was previously determined to distinguish between controls, patients with pulmonary tuberculosis, and those with lung cancer. One pfeRNA, previously shown to bind p60-DMAD and affect apoptosis, complements small nucleolar RNA SNORD45C, matching smaller 18S rRNA and lncRNA segments. Thus, pfeRNAs appear to have a common origin with known multifunctional ncRNA fragments. Differential modification may contribute to the multifunctionality of ncRNAs. For instance, for tRNA fragments, stabilizing 3′-end 2′-O-methylation, 3′-aminoacylation, and glycosylation modifications may regulate protein function, translation, and extracellular effects, respectively. One ncRNA gene can encode multiple fragments, multiple genes can encode the same fragment, and differentially modified ncRNA fragments might synergize or antagonize each other. Full article

Nickel-rich layered oxides such as LiNi_xMn_yCo_zO₂ (NMC), LiNi_xCo_yAl_zO₂ (NCA), and LiNi_xMn_yCo_zAl_{(1–x–y–z)}O₂ (NMCA), where x ≥ 0.6, have emerged as key cathode materials in lithium-ion batteries due to their high operating voltage and superior energy density. These materials, characterized by low cobalt content, offer a promising path toward sustainable and cost-effective energy storage solutions. However, their electrochemical performance remains below theoretical expectations, primarily due to challenges related to structural instability, limited thermal safety, and suboptimal cycle life. Intensive research efforts have been devoted to addressing these issues, resulting in substantial performance improvements and enabling the development of next-generation lithium-ion batteries with higher nickel content and reduced cobalt dependency. In this review, we present recent advances in material design and engineering strategies to overcome the problems limiting their electrochemical performance (cation mixing, phase stability, oxygen release, microcracks during cycling). These strategies include synthesis methods to optimize the morphology (size of the particles, core–shell and gradient structures), surface modifications of the Ni-rich particles, and doping. A detailed comparison between these strategies and the synergetic effects of their combination is presented. We also highlight the synergistic role of compatible lithium salts and electrolytes in achieving state-of-the-art nickel-rich lithium-ion batteries. Full article

Silicon oxynitride (SiO_xN_y, hereafter denoted as SiON) thin films represent an intermediate phase between silicon dioxide (SiO₂) and silicon nitride (Si₃N₄). Through systematic compositional ratio adjustments, the refractive index can be precisely tuned across a wide range from 1.45 to 2.3. However, the underlying mechanism governing the influence of elemental composition on film structural quality remains insufficiently understood. To address this knowledge gap, we systematically investigate the effects of key industrial plasma-enhanced chemical vapor deposition (PECVD) parameters—including precursor gas selection and flow rate ratios—on SiON film properties. Our experimental measurements reveal that stoichiometric SiO_xN_y (x = y) achieves a minimum surface roughness of 0.18 nm. As oxygen content decreases and nitrogen content increases, progressive replacement of Si-O bonds by Si-N bonds correlates with increased structural defect density within the film matrix. Capacitance–voltage (C-V) characterization demonstrates a corresponding enhancement in device capacitance following these compositional modifications. Recent studies confirm that controlled modulation of film stoichiometry enables precise tailoring of dielectric properties and capacitive behavior, as demonstrated in SiON-based power electronics, thereby advancing applications in related fields. Full article

Increased levels of reactive oxygen species (ROS) are a hallmark of cardiovascular disease. ROS impact the function of proteins largely through thiol modification leading to redox signalling. Acute, targeted interference with local ROS levels has been difficult. Therefore, how dynamics in redox signalling impact cardiovascular health is still a matter of current research. An inducible, endothelial cell-specific knock-in mouse model expressing a yeast D-amino acid oxidase enzyme was generated (Hipp11-Flox-Stop-Flox-yDAO-Cdh5-CreERT2^+/0 referred to as ecDAO). DAO releases H₂O₂ as a by-product of the conversion of D-amino acids into imino acids. The D-amino acid treatment of DAO-expressing cells therefore increases their intracellular H₂O₂ production. The induction of yDAO in the ecDAO mice was performed with tamoxifen. Subsequently, the mice received D-Alanine (D-Ala, 0.5 M) through drinking water, and the effects on ROS production and vascular and cardiac function were determined. ecDAO induction increased endothelial ROS production as well as ROS production in the lung, which is rich in endothelial cells. The functional consequences of this were, however limited: After minimally invasive myocardial infarction, there was no difference in the outcome between the control (CTL) and ecDAO mice. With respect to vascular function, three days of D-Ala slightly improved vascular function as demonstrated by an increase in the diameter of the carotid artery in vivo and decreased vessel constriction to phenylephrine. Fifty-two days of D-Ala induced cardiac remodelling, increased peripheral resistance, and overoxidation of peroxiredoxins. In conclusion, acute stimulation of endothelial ROS improves cardiovascular function, whereas prolonged ROS exposure deteriorates it. Full article

Polymer-matrix composites with ceramic fillers have various applications, one of which is the modification of the electric field. For this purpose, in this work, high-permittivity silicone composites with different polarization titanates were produced by mechanical mixing. The ceramic fillers chosen were CaCu₃Ti₄O₁₂, K_xFe_yTi_8−yO₁₆, and BaTiO₃ powders with high permittivity values and uniformly distributed in the polymer volume. Ceramic powders were studied by X-ray phase analysis and scanning electron microscopy methods. The proportion of ceramic powder was 25 wt.%. In parallel, composites were prepared with the addition of 25 wt.% glycerin. The functional properties of silicone composites were studied using the following parameters: the electrical strength and permittivity. The addition of all types of ceramic fillers, both together and without glycerin, led to a decrease in electrical strength (below 15 kV·mm⁻¹); the exception is the sample with the CCTO without glycerin (about 28 kV·mm⁻¹). The permittivity and the dielectric loss tangent of the composites increased as a result of the addition of fillers, especially noticeable in combination with glycerol in the low-frequency region. The obtained results are in good agreement with the literature data and can be used in the field of insulation in a high-permittivity layer to equalize equipotential fields. Full article

This study reports the synthesis, characterization, and catalytic performance of a series of catalysts of Ru supported on CeO₂-Y₂O₃ composites (Ru/CeYX; X = 0, 33, 66, and 100 wt.% Y₂O₃) for CO₂ hydrogenation. Supported material modification (Y₂O₃-CeO₂), by the Y₂O₃ incorporation, allowed a change in selectivity from methane to RWGS of the CO₂ hydrogenation reaction. This change in selectivity is correlated with the variation in the physicochemical properties caused by Y₂O₃ addition. X-ray diffraction (XRD) analysis confirmed the formation of crystalline fluorite-phase CeO₂ and α-Y₂O₃. High-resolution transmission electron microscopy (HR-TEM) and energy-dispersive X-ray spectroscopy (EDS) elemental mapping revealed the formation of a homogeneous CeO₂-Y₂O₃ nanocomposite. As the Y₂O₃ content increased, the specific surface area, measured by BET, showed a decreasing trend from 106.3 to 51.7 m² g⁻¹. X-ray photoelectron spectroscopy (XPS) of Ce3d indicated a similar Ce³⁺/Ce⁴⁺ ratio across all CeO₂-containing materials, while the O1s spectra showed a reduction in oxygen vacancies with increasing Y₂O₃ content, which is attributed to the decreased surface area upon composite formation. Catalytically, the addition of Y₂O₃ influenced both conversion and selectivity. CO₂ conversion decreased with increasing Y₂O₃ content, with the lowest conversion observed for Ru/CeY100. Regarding selectivity, methane was the dominant product for Ru/CeY0 (pure CeO₂), while CO was the main product for Ru/CeY33, Ru/CeY66, and Ru/CeY100, indicating a shift towards the reverse water–gas shift (RWGS) reaction. The highest RWGS reaction rate was observed with the Ru/CeY33 catalyst under all tested conditions. The observed differences in conversion and selectivity are attributed to a reduction in active sites due to the decrease in surface area and oxygen vacancies, both of which are important for CO₂ adsorption. In order to verify the surface species catalytically active for RWGS, the samples were characterized by FTIR spectroscopy under reaction conditions. Full article

To enhance the high-temperature oxidation resistance of molybdenum-based materials, Y₂O₃-CeO₂ co-modified silicide coatings were produced on molybdenum substrates using two-step pack cementation. The microstructure and phase composition of Y₂O₃-CeO₂ co-modified composite coatings were examined both before and after oxidation. A detailed analysis of the antioxidant properties of the co-modified coatings and the mechanisms behind the modifications was also conducted. The incorporation of 1.0 wt.% CeO₂ and 1.5 wt.% Y₂O₃ into the composite coatings resulted in a dense, non-porous, maximum-thickness microstructure. This microstructure is characterized by the uniform distribution of parallel MoSi₂ and MoB layers on the substrate. In particular, the coating containing 1.5 wt.% Y₂O₃ exhibited superior oxidation resistance, with a weight gain of 0.29 mg/cm² and an oxidation rate constant of 6.68 × 10⁻⁴ mg²/(cm⁴·h) after oxidation at 1150 °C for 255 h. During oxidation, a dense SiO₂ oxide film is formed through the cooperation of Y₂O₃ and CeO₂, inhibiting further Si diffusion into the substrate and reducing the formation of the Mo₅Si₃ layer. Full article

Catalytic alkane hydroxylation activities of the iron complex encapsulated into the micropore of the Y-type zeolite and mesoporous zeolites, the latter of which were obtained by the partial removal of aluminum and alkaline treatment, have been explored by using H₂O₂ as the oxidant. The iron complex with tris(pyridylmethyl)amine (=TPA) encapsulated into the micropore of the genuine Y-type zeolite was a more stable and effective cyclohexane hydroxylating heterogeneous catalyst compared to the corresponding copper analogue as well as the non-encapsulated homogeneous Fe-TPA complex. The chemical modification of the zeolite supports with the organic groups led to changing the catalytic activity depending on the size and the hydrophobic or hydrophilic nature of the added organic groups. When the content of water in the solvent was increased, the activity of the hydrophilic longer chain-modified catalyst was improved compared to that applied on the reaction with the non-aqueous solvent. The hydrophobic fluoroalkyl modifier located near the entrance of the micropore hindered the access of the substrate and aqueous H₂O₂ to the encapsulated iron complex site in the genuine Y-type zeolite. On the other hand, the hydrophobic modification effectively improved the activity of the catalyst with the zeolite support having higher amounts of mesopores. The synergistic effect of the wider bore diameters and the hydrophobic nature derived from the fluoroalkyl chains led to the concentration of the hydrocarbon substrate near the active iron complex. Full article

As new technologies are developed, the demand for rare earth elements (REEs) has increased, despite limited awareness of their significant impact on people and the environment. In this study, waste fly ash was used as a precursor to synthesize inorganic aluminosilicate polymers by adding an activator to the alumina and silica compounds of the ash. Due to their structure and adsorption potential, their application for the removal of selected REEs (Gd³⁺, Y³⁺, and Sc³⁺) from water has been investigated. A decrease in the intensity of the quartz peak at 2θ of 26.6° in the XRD spectrum and the disappearance of the albite and mullite peaks due to dissolution during alkaline activation in both modified samples were observed. The appearance of a peaks at 2θ of 29.3° and 39.3° corresponding to calcite in the modified sample indicates the presence of wood ash. A shifting of the band in the DRIFT spectrum to 1030 cm⁻¹ on the spectra of modified samples corresponds to the vibrations of Al-O and Si-O bonds and the formation of a polymeric network structure (Si-O-Si or Si-O-Al). According to pH_PZC values, thermodynamic and kinetic parameters, and chemical composition, the presumed mechanism of REE adsorption is chemisorption and ion exchange. The highest adsorption efficiencies (up to 95%) for all examined REEs in both single and mixed REE solutions were obtained from an alkali-activated mixture of fly ash and wood ash. The results of this research are significant for expanding knowledge about the removal of REEs from the environment, the reduction of waste ash by their modification, and their potential subsequent use in construction as additives. Full article

A new compound [Y₂(sq)₃(H₂O)₄] (Y-sq; sq = squarate (C₄O₄^2–)) was prepared and structurally characterized. Since the RE-sq family (RE = Y, Dy, Yb, Lu) gave isostructural crystals, the objective of this study is to explore the effects of diamagnetic dilution on the SIM behavior through systematic investigation and comparison of diamagnetically diluted and undiluted forms. The 1%-Diluted Dy compounds, Dy@Y-sq and Dy@Lu-sq, showed AC magnetic susceptibility peaks without any DC bias field (H_DC), whereas undiluted Dy-sq showed no AC out-of-phase response under the same conditions. The Orbach and Raman mechanisms are assumed in the Arrhenius plots, giving U_eff/k_B = 139(5) and 135(8) K for Dy@Y-sq and Dy@Lu-sq, respectively, at H_DC = 0 Oe. In contrast, Yb@Y-sq and Yb@Lu-sq behaved different; Yb@Y-sq can be regarded as a field-induced SIM because AC out-of-phase response was recorded only when H_DC was present. On the other hand, Yb@Lu-sq showed a relaxation independent from temperature around 2 K at H_DC = 0 Oe, possibly ascribed to a quantum-tunneling-magnetization mechanism. Applying H_DC = 400 Oe afforded U_eff = 61.2(14) and 62.5(16) K for Yb@Y-sq and Yb@Lu-sq, respectively. The Y/Lu matrix dependence may be related to spin–phonon coupling. The dilution technique is a facile and versatile tool for modification of SIM characteristics. Full article