Search Results (2,024)

Background/Objectives: Calcium–phosphorus metabolism is critical for skeletal development in weaned piglets. This study evaluated the effects of dietary 25-hydroxyvitamin D₃ (25-OH-VD₃) in combination with phytase and probiotics on mineral metabolism, bone development, and related molecular mechanisms in weaned piglets. Methods: Sixty 28-day-old weaned piglets (7.1 ± 1.30 kg) were randomly assigned to four dietary treatments for 31 days (including 3 days of acclimation): CON (basal diet + 50 µg/kg 25-OH-VD₃), HI (CON + 50 mg/kg phytase), CY (CON +10 mg/kg probiotics), HICY (CON + 50 mg/kg phytase + 10 mg/kg probiotics). Apparent calcium digestibility, serum biochemical indices, bone mineral density (BMD), and mRNA and protein expression of calcium–phosphorus transport- and metabolism-related genes in jejunal mucosa and kidney were assessed. Results: Compared with CON, piglets in the HI, CY, and HICY groups showed higher apparent calcium digestibility (p < 0.05). Serum transforming growth factor-β was elevated in CY and HICY (p < 0.05). HI enhanced metatarsal and toe BMD (p < 0.05) and upregulated jejunal solute carrier family 34, member 2 (SLC34A2) and SLC34A3 mRNA expression (p < 0.05). In contrast, HICY reduced mRNA expression of transient receptor potential cation channel subfamily V member 6 and calcium-binding protein D28k, as well as of calcium-binding protein D9k and cytochrome P450 27B1 in the kidney (p < 0.05). Renal calcium-sensing receptor protein abundance increased in CY (p < 0.05). Conclusions: Supplementation of 25-OH-VD₃ with phytase and/or probiotics improved calcium utilization and modulated key transport pathways, contributing to enhanced bone development in weaned piglets. These findings highlight coordinated nutritional regulation of mineral metabolism during early post-weaning growth. Full article

Rare-earth elements including the fifteen lanthanides, from lanthanum (La) to lutetium (Lu), together with scandium (Sc) and yttrium (Y), can act either as matrix cations or as active luminescent centers when incorporated into host lattices. Owing to their relatively large ionic radii, high coordination numbers, and structural stability, ions such as La, Lu, Sc, Y, and gadolinium (Gd) typically serve as matrix cations in rare-earth vanadate (REVO₄)-based phosphors, while other trivalent lanthanide (Ln³⁺) ions act as active luminescent centers. These REVO₄ phosphors have proved to be good host lattices for optically active Ln³⁺ ions giving strong luminescence assigned to absorption of the vanadate (VO₄³⁻) groups, and the efficient energy transfer between host lattice and Ln³⁺ ions. The unique electronic configuration of Ln³⁺ ions, particularly their unpaired 4f electrons, makes them ideal for applications in luminescence, magnetism, electronic and magnetic relaxation, and catalysis. Due to their complementary luminescent characteristics, Ln³⁺-doped REVO₄ phosphors have attracted significant attention in recent years. Their unique optical properties make them highly valuable across a broad spectrum of applications. This paper provides a comprehensive review of the state of the art in Ln³⁺ (Eu³⁺, Sm³⁺, Tm³⁺, Er³⁺, Ho³⁺, Tb³⁺, Nd³⁺, and Yb³⁺)-doped REVO₄ (RE = Y, Gd, Lu, La) phosphors. It examines current synthesis approaches, alongside the development of advanced strategies, and explores structural characteristics, innovative designs, and luminescent behavior, including both downconversion and upconversion processes and sensing applications, of the Ln³⁺-doped REVO₄ phosphors. Full article

Water is one of the most valuable resources on the planet; without it, life as we know it could not exist. Consequently, its increasing scarcity and pollution, which are mainly due to industrialization and changing consumption patterns, intensify the stress on water resources. At the same time, industrial activities contribute to water contamination with pollutants such as heavy metals, further reducing water availability. Due to their risks to human health and ecosystems, effective removal strategies are essential. Among the emerging approaches, polymer-based additive manufacturing (AM), commonly known as 3D printing (3DP), has gained attention for water treatment due to its versatility, precise control over structure and porosity, and ease of processing, while remaining at a low cost. Additionally, the polymers used have interesting adsorbent properties and allow for the incorporation of functional additives, further enhancing their performance. This review analyses the recent advances in 3D-printed polymeric materials for the removal of heavy metals and dyes, focusing on material composition, manufacturing technologies, geometry, removal mechanisms, performance, and regeneration. It was concluded that metal ions and cationic dyes are primarily removed through adsorption, due to interactions with negatively charged surfaces that are often enhanced by high-affinity additives. Anionic dyes are generally less effectively removed by adsorption and often rely on degradation mechanisms. However, adsorption of anionic dyes can occur, for instance when the adsorbent surface is modified to introduce positively charged functional groups. The ability of 3DP to create hierarchical porous structures combining micro-, meso-, and macropores improves fluid flow and contact area, thereby enhancing the removal efficiency. Full article

This study compared the regulatory effects of dietary supplementation with natural clinoptilolite (CLN) versus a dietary cation-anion difference (DCAD) regimen on calcium homeostasis in dairy cows during the last 21 days prepartum. Results showed that cows in the DCAD group exhibited significantly higher blood ionized calcium (iCa) and parathyroid hormone (PTH) concentrations than those in the CLN group (p < 0.05). Serum PTH concentrations displayed a declining trend in both groups prepartum, which deviates from the classical theory of compensatory PTH secretion, suggesting that alternative compensatory pathways may be involved in the regulation of calcium homeostasis during the periparturient period in dairy cows. Monitoring of calcium homeostasis and related metabolic parameters following postpartum oral calcium bolus administration revealed that the incidence of subclinical hypocalcemia in the DCAD group was 26%, lower than the 62% observed in the CLN group. However, blood iCa concentrations returned to normal levels more rapidly in the CLN group. Additionally, CLN supplementation was associated with more stable blood pH and lower prepartum serum potassium concentrations (p < 0.05) that remained within the physiological range, which may contribute to improved tissue sensitivity to PTH. Full article

The high-pressure structural evolution of Gd₂Ce₂O₇ has been studied by synchrotron X-ray diffraction (up to 31.8 GPa) and Raman spectroscopy (up to 38.9 GPa). A pressure-induced phase transition from cubic (space group Ia-3) to monoclinic (C2/m) crystal structure was observed to initiate at 11.3 GPa. This transition was primarily driven by the compression-induced cation rearrangement, which significantly altered the local coordination environment. The structural transformation proceeded via a gradual, continuous pathway and persisted up to the maximum experimental pressure of 31.8 GPa. Notably, the high-pressure phase remains stable upon complete decompression, confirming an irreversible structural transformation of Gd₂Ce₂O₇. Full article

Chitosan, owing to its abundant amino and hydroxyl functional groups, serves as an effective biosorbent for the removal of toxic metal(loid) ions from water. This review summarizes recent advances in chitosan-based adsorbents specifically for arsenate (As(V)) and copper ions (Cu(II)), with an emphasis on adsorption mechanisms and electrospun nanofiber technologies. A conceptual “charge adaptation–structure synergy” model is proposed to elucidate the distinct adsorption behaviors of chitosan toward anionic and cationic substances: under acidic conditions, As(V) adsorption is dominated by electrostatic attraction to protonated amino groups, whereas at pH values near or above the pKa, Cu(II) removal proceeds via synergistic chelation involving deprotonated amino and hydroxyl groups. Competitive and synergistic interactions in binary systems, particularly between As(V) and coexisting anions such as phosphate, are also discussed. Notably, the kinetic advantages of electrospun chitosan nanofibers are highlighted, with equilibrium times shortened from several hours to approximately 0.5–2.6 h. Key challenges and future research directions are further discussed, including scalable manufacturing and the treatment of complex wastewater matrices. Full article

A diverse range of 4-dimethylaminopyridinium (DMAP) bis(trifluoromethylsulfonyl)-amide ionic liquids with specific functionalities (alkyl, alkoxy, hydroxyalkyl and benzyl) were designed, characterized and compared with their pyridinium analogs in terms of their physical and radiolytic properties. The influence of the dimethylamino group on ionic liquid structure was investigated by X-ray diffraction and molecular dynamics simulations. The influence of the electron-donating ability of the dimethylamino-substituted cation is evident in the differences in the electronic density of states between the DMAP and pyridinium ILs. This leads to substantial changes in the radical transients observed in pulse radiolysis of the neat ILs. It was found that the DMAP salts were higher melting, more viscous and less conducting than their pyridinium analogs. However, the DMAP salts exhibited higher thermal stabilities and could therefore be useful for high-temperature applications. Full article

Zinc and iron are essential micronutrients in crop nutrition, and polymer-based nanogels have emerged as promising carriers to modulate their availability in sustainable agricultural systems. Here, a polymeric model receptor was designed to investigate how the nature and position of electron-donating (–NH₂) and electron-withdrawing (–NO₂) substituents control the recognition of Zn²⁺ and Fe²⁺ cations. Using a combination of density functional theory calculations, energy decomposition analysis with natural orbitals for chemical valence (EDA–NOCV), electrostatic potential (ESP) mapping, and quantum theory of atoms in molecules (QTAIM) method, the receptor–cation interactions are dissected into electrostatic, Pauli repulsion, orbital, and dispersion contributions. The results show that complex stability is governed mainly by orbital and electrostatic terms, with Fe²⁺ forming the most stable complex (−393.57 kcal mol⁻¹) with regard to a Zn²⁺ similar complex (−288.80 kcal mol⁻¹). Zn²⁺ complexes exhibit a broad tunability with substituent pattern. Electron-donating groups systematically strengthen both electrostatic and orbital components, whereas nitro substituents display a pronounced positional effect, ranging from strong destabilization to significant stabilization of Zn²⁺ binding. These findings establish molecular-level guidelines for engineering polymeric nanogels with tunable affinity and selectivity toward micronutrient cations in agricultural applications. Full article

Amphiphilic cationic lipids based on the 1,4-dihydropyridine (1,4-DHP) scaffold represent a versatile platform for the development of self-assembling delivery systems. In this work, a series of ten new amphiphilic 1,4-DHP derivatives bearing branched ester substituents at the 3,5-positions and quaternized cationic groups at the 2,6-positions were designed and synthesized. The effect of branched ester chain length and branching on nanoparticle formation was investigated. The self-assembling properties of the synthesized amphiphiles were evaluated by dynamic light scattering using an ethanol injection method. All compounds formed positively charged nanoparticles with hydrodynamic diameters ranging from 52 to 439 nm and polydispersity index from 0.194 to 0.452. Amphiphiles 14b–17b with 2-hexyldecyl substituents formed smaller particles, with an average diameter below 100 nm. Several derivatives exhibited good stability over a 14-day storage period at room temperature. To clarify structure–property relationships, lipophilicity (AlogP), polar surface area (PSA), and pK_a values were calculated using Schrödinger computational tools. The compounds displayed high lipophilicity AlogP 8.98–19.32, while PSA values remained within a narrow range. The calculated pK_a values ranged from 7.20 to 10.99. The results demonstrate that both the length and architecture of branched ester chains significantly influence nanoparticle size, homogeneity, and stability, highlighting branched-chain 1,4-DHP amphiphiles as promising synthetic lipid candidates for further development of delivery systems after evaluation of biological properties. Full article

Managing excessive water production in oil fields during primary, secondary, or enhanced recovery remains challenging. It increases costs and reduces hydrocarbon recovery, particularly in reservoirs with high-conductivity pathways such as high-permeability zones and fractures. Hydrogels are commonly used for water blocking and retention; however, their effectiveness diminishes at higher flow rates due to mechanical weaknesses and structural limitations. These problems are intensified under harsh environmental conditions, including high temperatures, salinity, and hardness. In this study, we investigate how altering the molecular suprastructure of preformed particle gel (PPG) can improve its effectiveness in shear-responsive water-blockage treatments, particularly when traditional PPGs cannot control rising flow rates. We enhance the shear-responsive mechanical properties of a composite PPG by increasing the density and diversity of intermolecular interactions. We use two different strategies: first, incorporating cationic groups into the polymer backbone to form a polyampholyte network with stronger electrostatic interactions; second, adding a linear anionic polymer to generate a secondary interpenetrating network that can undergo a coil–stretch transition under thermal and shear stimuli, thereby enhancing its own solvation and whole-network expansion. Molecular simulations provide an interpretation of the experimentally observed shear-thickening response and enhanced disproportionate permeability reduction at high flow rates. The water residual resistance factor of the improved PPGs deviates from the typical shear-thinning power-law behavior (n < 1) observed in conventional PPG, showing shear-thickening (n > 1). Tests reveal a strong ability to preferentially reduce water flow over oil, with Disproportionate Permeability Reduction increasing from 8 to 117 in the high-flow-rate zone. The enhanced strength and thermal stability also improve resistance to washout under high-pressure gradients. This research provides a novel approach to tailoring the microscopic architecture of PPGs to achieve selective, robust water blockage, offering a high-efficiency solution for complex reservoir environments. Full article

The purpose of our study was to assess if spinacetin (SPC), a flavonoid found in spinach, can alleviate the cyclophosphamide (CYP)-induced changes in cystometric and inflammatory parameters indicative of the development of hemorrhagic cystitis. The animal experiments were conducted in female Wistar rats. The cohort of 60 animals was grouped as follows: I—control, II—CYP group, III—SPC group, and IV—CYP + SPC group. The cystometry and biochemical analyses were performed after a fortnight of SPC administration. SPC was found to restore normal cystometric parameters in CYP-induced cystitis and, similarly, it normalized c-Fos expression changes in the central micturition regions. SPC further prevented a massive increase in the bladder wall thickness/permeability due to exposition to CYP administration. CYP instillation resulted in the elevation of biomarkers found in urine (brain-derived neurotrophic factor, BDNF, and nerve growth factor, NGF), and in the bladder detrusor muscle (Rho kinase and vesicular acetylcholine transporter, VAChT), which were successfully restored after administration of SPC. As for the biomarkers in the bladder urothelium, the CYP-induced increases in TNF-α, IL-1β, IL-6, calcitonin gene-related peptide (CGRP), malondialdehyde, 3-nitrotyrosine, insulin-like growth factor-binding protein 3 (IGFBP-3), occludin, organic cation transporter 3 (OCT-3), orosomucoid-1 (ORM1), pituitary adenylate cyclase receptor 1 (PAC1), synaptosomal-associated protein 23 (SNAP23), SNAP25, and synaptic vesicle glycoprotein (SV2A) levels were attenuated by SPC. Finally, CYP administration resulted in a decrease in the heparin-binding EGF-like growth factor (HB-EGF), hemopexin (HPX), T-H protein, and tight junction protein (Z01), and we noted the successful restoration of all these changes in concentrations after application of SPC. In summary, SPC robustly mitigated cyclophosphamide (CYP)-induced cystometric dysfunction and biochemical alterations characteristic of iatrogenic hemorrhagic cystitis. These findings position SPC as a compelling therapeutic candidate and warrant further translational investigation for the management of CYP-induced bladder injury. Full article

Hypochlorous acid (HClO) is widely used as a low-cost and effective disinfectant; however, its instability under heat and light necessitates simple and reliable monitoring methods. Herein, we report a morphology-evolving thin-film colorimetric sensor that enables intuitive visual detection of HClO through simultaneous color and pattern transitions. The sensor integrates two polymer films with distinct charge-state response behaviors, patterned in X-shaped and circular geometries on a single substrate. Upon exposure to HClO, chlorine-induced modification of amide and amine groups alters the surface charge states, thereby switching the adsorption preference for anionic and cationic dyes. This mechanism results in a pronounced transformation from a blue X-shaped motif to a red circular pattern, enabling direct visual discrimination between different HClO concentrations. Quantitative analysis of RGB values confirmed semi-quantitative detection in the sub-millimolar to millimolar range. The sensor exhibited a linear response in the range of 0–3 mM (R² > 0.979) with a limit of detection of 0.103 mM. The sensor further demonstrated practical applicability by tracking photodecomposition of a commercial disinfectant. This work demonstrates pattern-coupled colorimetric sensing as a straightforward, user-friendly approach for HClO monitoring. Full article

The structural characterization of GG-rich DNA sequences in presence of metal ions provides essential insight into quadruplex stability and ion-dependent conformational specifics. We report the crystal structure of the GG-quadruplex formed by the sequence GGGGTTTTGGGG in the presence of Zn²⁺, K⁺, and Na⁺. It was deposited in the RCSB Protein Data Bank under the accession code 9FTA. The structure was determined by single-crystal X-ray diffraction at a resolution of 2.49 Å in the space group P2₁2₁2₁. It reveals a parallel-stranded, two-G-tetrad stabilized by K⁺ ions within the central channel, while Na⁺ and Zn²⁺ occupy peripheral and groove-associated sites. Zn²⁺ ions are engaged in noncanonical coordination interactions with phosphate oxygens and structured water molecules, contributing to lattice stabilization and subtle adjustments in groove dimensions. The T4 loop forms a compact, ordered motif that contributes to crystal packing rather than intramolecular G4 stabilization. The presence of mixed cations produces a sole lattice architecture mediated by ions that provides structural insight into how bivalent and monovalent metals mutually modulate G-quadruplex topology. These results suggest a basis for understanding the specific ion effects on G4 structures and may direct the design of metal open DNA architectures. Full article

This study evaluated serum eosinophil cationic protein (ECP) as a biomarker for pediatric allergic airway diseases. A cross-sectional analysis was performed on children (1–17 years) with allergic asthma (AA, n = 124), allergic rhinitis (AR, n = 74), acute bronchitis (AB, n = 72), and healthy controls (HC, n = 58). Serum ECP, total IgE, eosinophil counts, allergen sensitization, and lung function were measured. Diagnostic performance was assessed using receiver operating characteristic (ROC) curves, and correlations among biomarkers were examined. Compared with HC, serum ECP levels were significantly elevated across all disease groups (AA, AR, and AB), with a particularly marked difference observed between AA and AR patients (p < 0.0001). The combination of ECP and IgE significantly improved the diagnostic accuracy for AA (AUC = 0.9494) and AR (AUC = 0.9501). Higher ECP levels were associated with increased sensitization to specific inhalant allergens and impaired pulmonary function, particularly in small airway indices. Serum ECP reflects eosinophil-mediated airway inflammation and enhances diagnostic performance for pediatric AA and AR, supporting its role as an auxiliary biomarker in evaluating pediatric allergic airway diseases. Full article

The removal of water pollutants, specifically the organophosphorus pesticides chlorpyrifos (CHP) and azinphos-methyl (AZM), as well as the dye Rhodamine B (RB), was investigated through the valorization of grape pomace, an abundant agricultural byproduct. For the first time, hydrochars derived from grape pomace were utilized as adsorbents for these contaminants following KOH activation (HCK) and pyrolysis at 400 °C (PHC). The study aimed to evaluate the adsorption performance, determine the optimal conditions, and elucidate the adsorption mechanisms. Physicochemical characterization using SEM, FTIR, BET surface area analysis, stability, and pH_PZC measurements revealed distinct differences in surface morphology, functional groups, porosity, and surface charge. Under optimized conditions, maximum adsorption capacities reached 751.0, 3.98, and 1.39 mg g⁻¹ for RB, CHP, and AZM, respectively, on HCK, and 616.0 (RB), 30.10 (CHP), and 9.15 mg g⁻¹ (AZM) on PHC, indicating that the selected hydrochars efficiently removed the investigated pollutants from water. Kinetic modeling demonstrated pseudo-first-order adsorption for RB and CHP on HCK and pseudo-second-order adsorption for AZM on HCK and all pollutants on PHC. Thermodynamic analysis confirmed that adsorption processes were spontaneous and favorable, with enhancements dependent on temperature. These findings suggest that HCK is particularly effective for cationic dyes, while PHC exhibits greater affinity toward organophosphorus pesticides, offering complementary applications and providing new mechanistic insights into hydrochar-based pollutant removal. Full article