Search Results (503)

Diagnosis of dengue virus infections typically relies on RT-PCR-based methods, for which reliable positive controls are essential. Viral RNA is an ideal positive control, but its inherent instability poses a major challenge. Herein, we report a simple and effective method for stabilizing dengue virus RNA by immobilizing it onto silk fibroin films (RNA-SFFs). We evaluated various substrate surfaces for RNA-SFFs preparation and found that the inner surface of sealable bags is optimal for uniform film formation and easy harvesting. Screening different silk fibroin concentrations revealed that even low concentrations (2.8%) effectively preserved RNA well and kept Ct constant for up to 16 days at 25 °C, 37 °C, and even 45 °C (extreme weather for transportations). Due to its rapid film formation and ease of peeling, 7% silk fibroin was selected. Notably, the RNA-SFFs demonstrated robust resistance to UV irradiation, with no significant Ct value changes after 4 h of exposure. Long-term stability testing at −20 °C, 25 °C, and 37 °C showed that dengue serotype 1–4 RNA-SFFs remained stable for the entire duration of the study—up to 56 weeks (approximately 14 months)—at all tested temperatures. These results demonstrate that RNA-SFFs are highly stable, portable, and practical as positive controls for dengue diagnostics, with strong potential for use in on-site and resource-limited settings. Full article

The optimization of the microstructural homogeneity and residual stress distribution in Ti sputtering targets for OLED 6G applications is essential for improving dimensional stability, durability, and deposition performance. Herein, 3N Ti plates were hot-rolled at 730 °C and then annealed at 600 °C and 700 °C for different durations to investigate the effects of annealing parameters on microstructural evolution and stress relaxation. X-ray diffraction analysis revealed that hexagonal α-Ti with progressive development of the (002) orientation was produced during annealing under all the conditions. Electron backscatter diffraction analyses showed that short-time annealing at 600 °C (≤30 min) generated heterogeneous grains, high dislocation density, and mixed grain boundary character, whereas extended annealing (≥60 min) produced a more uniform microstructure. However, residual stress differences between the plate center and edge remained significant under this condition. Conversely, annealing at 700 °C promoted progressive recrystallization, as indicated by increased high-angle grain boundary fractions and decreased kernel average misorientation values, and facilitated grain growth stabilization across the plate. Prolonged annealing improved microstructural and residual stress uniformity significantly, and near-complete homogenization was achieved after 5 h. These findings demonstrate that annealing at 700 °C for sufficient time is optimal for producing homogeneous microstructures and uniform residual stress distributions, providing valuable guidelines for Ti sputtering target processing. Full article

As a favorable hydrophilic additive for antifouling modification of polyvinylidene fluoride (PVDF) membrane, titanium dioxide (TiO₂) nanoparticles have been applied for years. Sodium dodecyl sulfonate (SDS), a representative anionic surfactant, has been proven to benefit the dispersion of nano-TiO₂ via an electro-spatial stabilizing mechanism. In this study, various proportionally SDS-functionalized TiO₂ nanoparticles were adopted to modify PVDF membrane. Dispersion and stability of SDS-functionalized TiO₂ nanoparticles in casting solutions were evaluated by multiple light scattering technology. The properties and antifouling performance of PVDF/SDS-TiO₂ composite membranes were assessed. The uniformity of surface pores as well as structures on cross-section morphologies was modified. The finger-like structure of PVDF/SDS-TiO₂ composite membrane was adequately developed at the SDS/TiO₂ mass ratio of 1:1. The improved antifouling performance was corroborated by the increasing free energy of cohesion and adhesion as well as the interaction energy barrier between membrane surfaces and approaching foulants assessed by classic extended Derjaguin–Landau–Verwey–Overbeek (XDLVO) theory, the low flux decline during bovine serum albumin (BSA) solution filtration process, and the high critical flux (38 L/(m²·h·kPa)) in membrane bioreactor. This study exploits a promising way to modify PVDF membrane applicable to the wastewater treatment field. Full article

The present work investigates the electrochemical behavior of the Zr2.5Nb alloy in a biomedical context, emphasizing the influence of electrochemical oxidation treatment on its stability in simulated physiological environments. The alloy samples were oxidized in 1 M H₂SO₄ under controlled voltages (200–275 V) and times (1 min), identifying 200 V–1 min as the optimal condition for obtaining a uniform porous oxide layer with an average pore diameter of ~90 nm. The corrosion resistance was evaluated using open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) in Ringer’s solution and Ringer’s solution containing 40 g/L H₂O₂ to simulate physiological and inflammatory conditions. Electrochemical tests revealed that electrochemically oxidized samples exhibited a polarization resistance up to 14.78 MΩ·cm², about 26 times higher than that of the untreated alloy (0.56 MΩ·cm²). After 77 h of immersion, the oxidized alloy maintained a high resistance (17.54 MΩ·cm²), confirming long-term stability. Scanning Electron Microscopy (SEM–EDX) and X-Ray Diffraction (XRD) analyses highlighted significant increases in oxygen content and the transformation from the monoclinic baddeleyite to the cubic arkelite phase of ZrO₂, contributing to enhanced corrosion resistance. These findings demonstrate that controlled electrochemical oxidation significantly improves the durability of Zr2.5Nb alloy in oxidative environments, supporting its potential for long-term biomedical implant applications. Full article

Superparamagnetic iron oxide nanoparticles (SPIONs) with sizes below 10 nm are biocompatible and non-toxic, making them promising for biomedical applications. To prevent their agglomeration and enhance their functionality, the nanoparticles were coated with citric acid (CA), which modifies the surface charge, improves dispersion stability, and facilitates biomedical use. In this work, a modular flow-through microreactor system was employed to synthesize and coat the nanoparticles in a single, continuous two-step process. The system enables precise control over temperature and mixing, ensuring uniform reaction conditions and minimizing hot spots. The synthesized Fe₃O₄ nanoparticles exhibited an average crystallite size of ~5 nm (XRD) and particle sizes of 4–6 nm (TEM). FTIR analysis confirmed the successful surface functionalization with CA, while TGA indicated a coating mass fraction of approximately 4–20 wt%, increasing with higher CA concentration. Zeta potential measurements revealed strong colloidal stability, with values around −35 mV at pH 6.5. Among the tested CA concentrations, the sample with a molar ratio of Fe₃O₄:CA = 1:0.25 exhibited the most favorable properties, including narrow size distribution and improved dispersion stability. These findings demonstrate that the continuous modular flow approach enables the reproducible synthesis of highly stable, sub-10 nm CA-coated SPIONs, offering promising potential for biomedical applications, particularly as magnetic resonance imaging (MRI) contrast agents. Full article

This study aimed to investigate the interactions between soluble soybean polysaccharides (SSPS) and milk proteins, namely, casein and whey protein, and to evaluate their effects on the stability of acidified milk beverages under different degrees of thermal denaturation. Casein, whey protein, and SSPS were used as raw materials to prepare mixed solutions under varying pH conditions. A combination of analytical techniques, including centrifugal sedimentation rate, particle size distribution, ζ-potential measurement, differential scanning calorimetry (DSC), size-exclusion chromatography (SEC), and LUMisizer stability analysis, was employed to systematically examine the interactions between SSPS and the two proteins, as well as the influence of thermal treatment at 120–140 °C (casein) and 65–78 °C (whey protein). The results demonstrated that under acidic conditions (pH 3.5–4.5), SSPS formed compact complexes with casein, effectively stabilizing casein dispersions through steric hindrance and electrostatic repulsion. In contrast, SSPS exhibited a limited stabilizing ability toward whey protein due to its strong tendency to aggregate, which hindered the formation of uniform complexes. Regarding thermal denaturation, casein heated at 140 °C for more than 40 min showed pronounced κ-casein dissociation and aggregation, resulting in reduced stability of the SSPS–casein system. For whey protein, increasing thermal denaturation (complete denaturation at 78 °C for 30 min) led to the formation of larger aggregates, with particle size increasing from 198.23 nm to 213.33 nm and ζ-potential decreasing from −3.77 mV to −2.01 mV, thereby diminishing the stability of the SSPS–whey protein system. Overall, this study elucidates the interaction mechanisms of SSPS with casein and whey protein, and highlights the role of thermal denaturation, thereby providing theoretical guidance for the effective application of SSPS in acidified milk beverages. Full article

The reliance on carbon-based fuels remains a major contributor to greenhouse gas emissions, emphasizing the need for sustainable alternatives such as hydrogen. Sodium borohydride (NaBH₄), with a hydrogen content of 10.6 wt%, is a promising chemical hydrogen storage material capable of releasing four moles of H₂ per mole through hydrolysis; however, effective catalysts are essential for practical implementation. In this study, silver nanoparticles supported on glucose-derived carbon microspheres (AgSC) were synthesized and evaluated for catalytic NaBH₄ hydrolysis. Structural characterization (XRD, TEM, SEM, EDS) confirmed the uniform dispersion of metallic silver nanoparticles on the carbon support with no detectable Ag₂O phase. AgSC exhibited superior catalytic activity compared to unsupported Ag or bare carbon, achieving the highest hydrogen generation under neutral pH, elevated temperatures, and 835 µmol NaBH₄. The catalyst displayed an activation energy of 54 kJ mol⁻¹, turnover numbers (TONs) of 1.4 × 10⁵–1.9 × 10⁵, and turnover frequencies (TOFs) of 7.1 × 10⁴–9.3 × 10⁴ h⁻¹, demonstrating efficient utilization of active sites. pH-dependent studies revealed optimal hydrogen yield under neutral conditions, while acidic and basic media reduced performance due to surface poisoning and BH₄⁻ stabilization, respectively. Reusability tests showed only ~5% activity loss after five cycles. These findings establish AgSC as a stable, efficient, and recyclable catalyst for on-demand hydrogen generation, supporting sustainable clean fuel technologies. Full article

This study presents a green and sustainable approach for synthesizing zinc oxide nanoparticles (ZnO-NPs) using Melia azedarach leaf extract as a reducing and stabilizing agent, with zinc acetate as the precursor. The synthesized nanoparticles were thoroughly characterized to assess their structural, morphological, and physicochemical properties, revealing nanoscale dimensions, enhanced crystallinity, and improved stability compared to commercial ZnO. Controlled release experiments under plant-relevant pH conditions demonstrated a gradual and sustained release of Zn²⁺ ions, accompanied by buffering effects and re-precipitation of Zn(OH)₂, highlighting their potential for long-term nutrient availability in soil systems. Unlike conventional studies that focus mainly on synthesis or characterization, this work emphasizes the functional performance of ZnO-NPs as nanofertilizers, combining eco-friendly production with practical agricultural applications. The plant-mediated synthesis yielded nanoparticles with uniform size distribution, enhanced dispersion, and stability, which are critical for efficient nutrient delivery and persistence in soil. Overall, this study provides a cost-effective, scalable, and environmentally benign strategy for producing ZnO nanoparticles and offers valuable insights into the development of sustainable nanofertilizers aimed at improving crop nutrition, soil fertility, and agricultural productivity. Full article

A highly active Co/Beta catalyst was prepared via ion-exchange method, in which sodium cations in the beta zeolite framework were replaced by cobalt ions using an aqueous cobalt nitrate solution. Based on XRD, SEM, TEM, XPS, and nitrogen adsorption–desorption analyses, it was confirmed that cobalt species successfully took the place of sodium ions in beta zeolite, while the cobalt species diffused with a uniform dispersion. Strong electronic coupling between cobalt species and zeolite framework oxygen stabilizes Co²⁺ sites in the material. The catalysts perform high efficiency in dye Acid Orange II (AO7) degradation reactions, which gives more than 99.5% removal efficiency at room temperature and initial pH within 10 min under low catalyst dosage. The advantages of the Co/Beta catalyst are reasonably attributed to its maximized metal−zeolite synergistic efficiency. Full article

Culinary herbs and spices are highly valued for their contribution to aroma, color, and overall flavor in traditional foods. Microbial inactivation in fresh herbs and spices is challenging due to their complex surface structures and dense natural microflora, which limit the effectiveness of conventional methods. Atmospheric cold plasma (ACP) is an innovative non-thermal technology with potential applications in the fresh spice industry. This study investigates the efficacy of ACP, generated using a practical, simple, and original system that allows uniform treatment without complex equipment, on microbial inactivation and quality attributes of fresh spices. Treatments of 1 and 3 min were applied, and their effects on natural microflora, Escherichia coli, and Pseudomonas syringae spp. were evaluated on the first day and after 7 days of storage. Results showed that 3 min treatments achieved higher reductions in natural microflora (2.91 log CFU g⁻¹), E. coli (2.76 log CFU g⁻¹), and P. syringae spp. (2.24 log CFU g⁻¹) compared to 1 min treatments (1.87, 1.93, and 1.65 log CFU g⁻¹, respectively). Different herbs exhibited varying responses to ACP, reflecting differences in leaf structure and chemical composition, which highlights the need for tailored treatment strategies. ACP treatment did not significantly affect water activity, color, or moisture content (except for rosemary, bay leaf, and thyme), nor total anthocyanin content (TAA), total phenolic content (TPC), total antioxidant capacity (TAC), or total flavonoid content (TFC). However, total chlorophyll content (TCC) and pH increased significantly in most samples (except rosemary and dill). Scanning electron microscopy (SEM) revealed that the tissue integrity of rosemary and mint was affected by ACP, although more than 50% of carvone in mint was preserved, and its concentration increased. The observed microbial reductions and 3–8-day shelf-life extension suggest meaningful improvements in safety and storage stability for industrial applications. Overall, ACP demonstrates promise as a safe, efficient, and scalable alternative to conventional decontamination methods, with broad potential for enhancing the quality and shelf life of fresh spices. Full article

Organophosphate pesticides are among the most persistent and toxic contaminants in aquatic environments, requiring effective strategies for detection and remediation. In this work, density functional theory (DFT) calculations were employed to investigate the adsorption of nine representative organophosphates (glyphosate, malathion, diazinon, azinphos-methyl, fenitrothion, parathion-methyl, disulfoton, tokuthion, and ethoprophos) on mercaptobenzothiazole disulfide (MBTS) and MBTS-functionalized graphene (G–MBTS). All simulations were performed in aqueous solution using the SMD solvation model with dispersion corrections and counterpoise correction for basis set superposition error. MBTS alone displayed a range of affinities, suggesting potential selectivity across the organophosphates, with adsorption energies ranging from 0.27 to 1.05 eV, malathion being the strongest binder and glyphosate the weakest. Anchoring of MBTS to graphene was found to be highly favorable (1.26 eV), but the key advantage is producing stable adsorption platforms that promote planar orientations and $\pi$–$\pi$/dispersive interactions. But the key advantage is not stronger binding but the tuning of interfacial electronic properties: all G–MBTS–OP complexes show uniform, narrow HOMO-LUMO gaps (∼0.79 eV) and systematically larger charge redistribution. These features are expected to enhance electrochemical readout even when adsorption strength was comparable or slightly lower (0.47–0.88 eV) relative to MBTS alone. A Quantum Theory of Atoms in Molecules (QTAIM) analysis of the G–MBTS–malathion complex revealed a dual stabilization mechanism: multiple weak C–H⋯$\pi$ interactions with graphene combined with stronger S⋯O and hydrogen-bonding interactions with MBTS. These results advance the molecular-level understanding of pesticide–surface interactions and highlight MBTS-functionalized graphene as a promising platform for the selective detection of organophosphates in water. Full article

Aflatoxin B1 (AFB1) and its metabolite aflatoxin M1 (AFM1) are stable and carcinogenic mycotoxins that are commonly found in dairy products, posing serious food safety concerns. However, conventional degradation methods face limited degradation efficiency and high energy demand. Here, we develop an innovative polyvinylidene fluoride (PVDF) composite membrane incorporating Fe/Co-based metal-organic frameworks (MOF) (Named Fe/Co-MIL-88B(NH₂)) and CaO₂ for targeted aflatoxin removal from milk. This system integrates two synergistic mechanisms: (1) hierarchical porous MOF structures enabling superior aflatoxin adsorption capacity and peroxidase-like catalytic activity, and (2) CaO₂ acts as a controllable-release H₂O₂ donor, supplying a steady flux of reactive oxygen species without the addition of exogenous H₂O₂. Moreover, the PVDF membrane with mechanical stability offers uniform immobilization of active components, which prevents the aggregation of nanozymes. As a result, the integrated membrane achieves high degradation efficiency for AFB1 and AFM1, exceeding 95% within 60 min. By eliminating external oxidant addition and minimizing collateral nutrient damage, the technology demonstrates remarkable operational stability (>10 cycles) and milk quality preservation capability. This breakthrough establishes an efficient and reusable detoxification method, providing new opportunities for mycotoxin mitigation in dairy products through spatiotemporal control of reactive oxygen species. Full article

Background/Objectives: Lidocaine hydrochloride (LD-HCl) is the most commonly used local anesthetic in dentistry, often administered with epinephrine to extend its duration and reduce systemic absorption. However, its relatively short duration of action, the need for repeated injections, and the unpleasant taste may limit patient compliance and procedural efficiency. This study aimed to develop and evaluate a novel injectable nanoemulsion-based in situ gel depot system of LD to provide prolonged anesthetic activity. Methods: LD-loaded nanoemulsions were formulated by high-shear homogenization followed by probe sonication, employing Miglyol 812 N (oil phase), a combination of Tween 80 and soy lecithin (surfactant–co-surfactant), glycerin, and deionized water (aqueous phase). The selected nanoemulsion (S1) was dispersed in a thermoreversible poloxamer solution to form a nanoemulgel. The preparation was evaluated for globule diameter and uniformity, zeta potential, surface morphology, pH, drug content, stability, rheological behavior, injectability, and in vitro drug release. Analgesic efficacy was assessed via tail-flick and thermal paw withdrawal latency tests in Wistar rats. Cardiovascular safety was monitored using non-invasive electrocardiography and blood pressure measurements. Results: The developed nanoemulsions demonstrated a spherical shape, nanometer size (206 nm), high zeta-potential (−66.67 mV) and uniform size distribution, with a polydispersity index of approximately 0.40, while the nanoemulgel demonstrated appropriate thixotropic properties for parenteral administration. In vitro release profiles showed steady LD release (5 h), following the Higuchi model. In vivo studies showed significantly prolonged analgesic effects lasting up to 150 min (2.5 h) compared to standard LD-HCl injection (p < 0.001), with no adverse cardiovascular effects observed. Conclusions: The developed injectable LD in situ nanoemulgel offers a promising, patient-friendly alternative for prolonged anesthetic delivery in dental and operative procedures, potentially reducing the need for repeated injections and enhancing procedural comfort. Full article

Methane dry reforming (DRM) represents a promising route for the simultaneous valorization of CH₄ and CO₂ into syngas; however, conventional Ni-based catalysts suffer from rapid deactivation due to sintering and carbon deposition. In this work, we present a synergistically engineered Ni-based catalyst integrating hierarchical SiC confinement, Pd promotion via oleic-acid-assisted complexation, and MgO surface modification to overcome these challenges. Under optimized reaction conditions (CH₄/CO₂ = 1:1, 750 °C, GHSV = 36,000 mL g⁻¹ h⁻¹), the multifunctional NiPd/Si–xMg catalyst achieved steady-state conversions of 85% for CH₄ and 84% for CO₂, maintaining an H₂/CO ratio close to 1.0 over 100 h of continuous operation without noticeable deactivation. In contrast, the reference Ni/SiC and Ni/MgO catalysts exhibited initial conversions of 75–80% but declined by more than 50% within the same period, confirming the superior durability of the optimized system. Thermogravimetric analysis (TGA) revealed a drastic reduction in carbon deposition—from 119.0 mg C g⁻¹ for Ni/SiC to 81.4 mg C g⁻¹ for NiPd/Si-xMg—indicating enhanced coke resistance. Transmission electron microscopy (TEM) confirmed uniform Ni dispersion with an average particle size of 7.2 ± 1.8 nm, while H₂-TPR and CO₂-TPD analyses demonstrated improved reducibility and surface basicity. The combination of SiC confinement, Pd-induced hydrogen spillover, and MgO-mediated CO₂ activation effectively mitigated sintering and carbon accumulation, resulting in high activity, stability, and carbon tolerance. This integrated catalyst design provides a robust pathway toward industrially viable DRM systems for sustainable syngas production. Full article

Electrospun fibers serve as a medium for the targeted release of active compounds, facilitating the desired therapeutic effects in drug administration. The point of this study was to find the best conditions for making electrospun fibers from cellulose acetate (CA) and poly(ε-caprolactone) (PCL), mixed with pure oxyresveratrol extract from Artrocarpus lakoocha Roxberg (Moraceae). Additionally, the study focused on evaluating the antioxidant properties, antityrosinase activity, and freeze–thaw stability of the resulting fibers. We incorporated a concentration of oxyresveratrol at 0.1% w/w into various mass ratios of CA/PCL blended fiber sheets (1:0, 3:1, 1:1, 1:3), utilizing mixed solvents of acetone/DMF (2:1% v/v) and chloroform/DMF (9:1% v/v) for preparation. The fiber sheets displayed a continuous and uniform structure, with fiber diameters ranging from 300 to 1000 nanometers. We investigated the release kinetics of oxyresveratrol from the fibrous substrates using the total immersion technique, specifically in phosphate-buffered saline at a pH of 7.4. The results showed that the fiber sheet with a 3:1 w/w ratio of CA to PCL and a 0.1 w/w loading of oxyresveratrol showed the most significant release of oxyresveratrol at the 2 h mark, and it continued to release consistently at this peak value for up to 24 h. The antioxidant and anti-tyrosinase properties of oxyresveratrol in fiber sheets were more stable than those of free oxyresveratrol at the same concentrations. The fiber sheet presents a promising avenue for a user-friendly transdermal patch application. Full article