Search Results (2,306)

In this study, we investigated how co-solvent and polymer combinations affect the performance of dye-sensitized solar cells (DSSCs) using TiO₂- and ZnO-modified carbon nanotube (CNT) composite papers as photoelectrodes. Co-solvents such as N,N-dimethylformamide (DMF) and ethylene glycol (EG) were incorporated into polyethylene glycol (PEG)- and poly(ethylene oxide) (PEO)-based gel electrolytes to increase the amount of dissolved I₂/KI redox species and evaluate their influence on the wettability of the electrolyte on CNT composite paper electrodes. PEG-based electrolytes containing DMF or EG improved the fill factor (FF) and power conversion efficiency (PCE) relative to the baseline formulation, with the EG–PEG electrolyte achieving the best single-device PCE of 15.58 × 10⁻³% using the CNT/ZnO composite paper. Replacing PEG with PEO or using PEG + PEO blends led to reduced performance, possibly because the modified polymer composition affected electrolyte wetting, spreading behavior, and penetration into the porous electrode. These results suggest that the wettability and viscosity-related behavior of gel electrolytes are important empirical factors associated with the performance of flexible paper DSSCs, and provide practical guidance for the design of paper-based photovoltaic devices. Full article

Microplastics have emerged as a major environmental health concern due to their environmental persistence, fragmentation, and widespread distribution. Conventional adsorption strategies often have limited efficiency, reuse, and scalability, and may generate secondary pollutants. This work explores the use of ferrotitaniferous sand milled for 4, 8, 12, 16, 32, and 52 h and subsequently functionalized with polyethylene glycol (PEG) for the removal of Polyethylene Terephthalate(PET) microplastics. The samples were characterized using Fourier-Transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM). The average particle size of the samples decreases with the milling time from $60\pm 35$ μm to $3\pm 1$ μm. The magnetic properties enable rapid separation of sand–microplastic aggregates from water using magnets. Ferrotitaniferous sand exhibits soft ferrimagnetic behavior, with a maximum saturation of 50.09 emu/g. The remanence and coercivity increase as the average particle size decreases. Ultraviolet–visible (UV-Vis) spectroscopy was used to quantify the hydrothermally fragmented PET microparticles in water. The maximum microplastic adsorption removal was 95% within 30 s for the 12 h milled sample coated with PEG. The results show that PEG increases the samples’ adsorption capacity from 20.48 to 32.36 mg/g. The novelty of this work lies in the use of magnetic Ferrotitaniferous sands as a promising, sustainable resource for magnetic separation technologies. Full article

Porcine epidemic diarrhea (PED), caused by the PED virus (PEDV), remains one of the most devastating diseases in the swine industry, with a mortality rate approaching 90–100% in suckling piglets due to severe dehydration and electrolyte imbalances. Passive immunization with egg yolk antibodies (IgY) represents a promising therapeutic strategy. In this study, we developed a novel recombinant adenovirus, rADM-IFN-G-ped, co-expressing selected antigenic regions of the PEDV S protein and chicken interferon-gamma (ChIFN-γ) as a molecular adjuvant. Laying hens were immunized with this construct to produce PEDV-specific IgY, which was subsequently purified from eggs using a polyethylene glycol (PEG-6000) precipitation method. The induced IgY demonstrated potent neutralizing activity against PEDV in vitro, with a neutralization titer (NT₅₀) of 1:96, which was significantly higher than that of IgY derived from hens immunized with a commercial inactivated PEDV G2b vaccine (NT₅₀ = 1:52). In a passive immunization and challenge trial, piglets treated with the rADM-IFN-G-ped-derived IgY exhibited significantly reduced fecal viral RNA shedding following challenge with the virulent PEDV-NX-2022 strain, compared to control groups. Crucially, while all piglets in the challenge control group succumbed to infection within 72 h, a 50% survival rate was achieved in the IgY-treated group. Histopathological examination of intestinal tissues further confirmed the protective efficacy, showing that IgY treatment markedly alleviated villous atrophy, epithelial necrosis, and inflammatory cell infiltration in the small intestine. These findings demonstrate that vaccination of laying hens with the rADM-IFN-G-ped recombinant adenovirus elicits a robust immune response, enabling the production of protective IgY. This proof-of-concept study establishes the viability of the multi-epitope adenoviral IgY platform as a passive immunization strategy against PEDV. Full article

The widespread use of proton pump inhibitors (PPIs) in clinical practice has increased the number of related hypersensitivity reactions (HSRs). The active ingredient is not always responsible for the reaction. In some cases, HSRs may be related to the excipients contained in the drug. The adverse reactions to anti-SARS-CoV-2 vaccines have drawn the scientific community’s attention to the potential roles of excipients such as polyethylene glycol (PEG) and polysorbate 80. We present a case of a patient with three anaphylactic reactions following the administration of the anti-SARS-CoV-2 vaccine and a history of HSR to omeprazole. Through an in-depth medical history and allergy testing, we found that the patient was sensitized to PEG contained in the vaccine and to the omeprazole formulation used. We also conducted a mini-review of the literature, reporting all cases of reactions to PPIs, both related to the active ingredient and to excipients. Adverse reactions to PPIs are rare but still increasing. To our knowledge, this is the first reported case of anaphylaxis to PPI-related PEG. Some excipients are widely used in commonly used products, including non-pharmaceuticals. Therefore, in patients with multiple episodes of anaphylaxis, it appears necessary to exclude a possible allergy to excipients. This could ensure a greater safety and a better quality of life. Full article

Osteoarthritis is the most prevalent age-related joint disease, yet the limited regenerative capacity of articular cartilage severely constrains spontaneous repair. Here, we present a freeze–thaw polyvinyl alcohol (PVA)/polyethylene glycol (PEG) hydrogel platform featuring a hybrid open–closed macroporous architecture that enables cartilage-mimetic load dissipation for artificial cartilage applications. The hybrid porous structure provides synergistic advantages, where closed pores enhance load-bearing stiffness while open pores facilitate energy dissipation. By systematically tuning polymer composition and processing conditions, clear structure–property relationships among porosity, water content, and mechanical performance are established. An optimized formulation (18 wt.% PVA, 85–124 kDa; 18 wt.% PEG; three freeze–thaw cycles) yields hydrogels with high water content (39.1 ± 7.8 wt.%), high compressive Young’s modulus (3.60 ± 0.67 MPa), and excellent resilience under cyclic loading. Notably, under dynamic compression (2 m/s), a frequently overlooked yet physiologically relevant mechanical property of hydrogels, the materials exhibit nearly twofold enhancement in compressive modulus compared to static conditions, demonstrating pronounced strain-rate-dependent stiffening. Finite element analysis reveals efficient load redistribution across the interconnected porous network, providing mechanistic insight into the observed mechanical robustness. Compared with native cartilage and recently reported hydrogel systems, the developed hydrogels exhibit superior stiffness while maintaining mechanical and structural resilience. In vitro cytotoxicity and direct-contact assays confirm excellent cytocompatibility. These results establish a scalable and cost-effective design strategy for engineering mechanically robust, rate-adaptive hydrogels, advancing the development of next-generation artificial cartilage substitutes. Full article

Eco-friendly biocomposites were prepared from poly(lactic acid) (PLA) plasticized with polyethylene glycol (PEG) and reinforced with Moroccan sugarcane bagasse fibers at 5, 10 and 15 wt%. The aim was to enhance PLA ductility through PEG incorporation while valorizing locally available lignocellulosic residues. Two processing methods, injection molding and melt extrusion additive manufacturing (MEX, 3D printing), were employed to investigate the influence of manufacturing method on the morphological, thermal, rheological and mechanical properties of the composites. Thermal analysis confirmed that PLA maintained its stability within the processing temperature range, supporting its suitability for MEX. Morphological observations revealed improved fiber dispersion and reduced porosity in injection-molded samples, whereas MEX-printed parts exhibited visible interlayer voids. These microstructural differences explained the superior tensile strength and modulus of injection-molded specimens compared to MEX ones. Full article

Local pulmonary delivery offers a non-invasive application route for mRNA therapeutics with the potential for high bioavailability at the target-site of applications such as mucosal vaccination or the treatment of lung diseases. However, efficient delivery remains challenging due to major lung-specific barriers, particularly mucus. Herein, pH-responsive, amphiphilic xenopeptides comprising lipoamino fatty acids and oligoamino acids (OAAs) connected in distinct branched U-shape or bundle topologies were evaluated as mRNA polyplexes for delivery to A549 and Calu-3 lung cells under standard submerged or air–liquid interface (ALI) transfection conditions, and upon intratracheal application in BALB/c mice. Optionally, polyplexes were coated with negatively charged hyaluronic acid (HA) or colloidally stabilized with poly(ethylene glycol) (PEG). For U-shapes, hydrophobic modification of the OAA domain boosted their efficiency. Interestingly, best-performing formulations varied across transfection conditions. While the bundle topology showed the highest potential in submerged cell culture, U-shaped carriers were more efficient under ALI conditions. Polyplex surface modification with HA or PEG did not strongly alter in vitro transfections, whereas hydrophobized U-shape core polyplexes combined with surface modification enhanced their efficiency in vivo. Thus, the cationizable core and surface properties of mRNA nanoparticles require specific balancing in various lung cell models and lung. Full article

A critical challenge in coalbed methane (CBM) extraction is the severe formation damage induced by conventional foam fracturing fluids, primarily through polymer retention and hydrogen bond disruption within the microporous matrix. This study presents a molecularly engineered, low-damage foam fracturing fluid that leverages synergistic nanoparticle–surfactant interactions to construct a robust interfacial pseudo-gel network, thereby decoupling effective fracture stimulation from adverse geochemical damage. The primary novelties of this work are threefold: (i) establishing a direct, quantitative cause-and-effect relationship between molecular interfacial architecture and reservoir protection, (ii) proposing a comprehensive “interfacial control” design paradigm that engineers viscoelasticity at the gas–liquid interface rather than through bulk polymer gelation, and (iii) demonstrating the complete decoupling of foam stability from formation damage in a polymer-free system. A systematic optimization methodology was employed: initial foaming agents were screened via the Waring Blender method, evaluating foam volume, half-life, and a derived comprehensive index; subsequently, synergistic binary surfactant mixtures and foam stabilizers were assessed to formulate the final systems. An optimized formulation, designated Foam System I (0.5 wt.% fluorosurfactant FK + 0.5 wt.% nano-silica RX + 2.0 wt.% KCl), demonstrated exceptional foam quality (Γ = 77.1 ± 1.5%) and kinetic stability (T₁/₂ > 350 s). Rheological characterization confirmed shear-thinning behavior conforming to the Herschel–Bulkley model (n = 0.38–0.42, R² > 0.98) and a structural recovery of 92.5 ± 2.1%—comparable to crosslinked polymer gels but achieved without any bulk viscosifier. Core flood analyses revealed that Foam System I induced a permeability damage of only 12.75 ± 1.8%, representing a 55–75% reduction compared to polyethylene glycol (PEG)-stabilized reference fluids (28.36–51.91%). X-ray photoelectron spectroscopy (XPS) correlated this enhanced reservoir compatibility with an 18.0 ± 2.0% suppression of oxygen-containing functional group adsorption, attributed to the steric hindrance conferred by the fluorinated hydrophobic moieties. This work establishes an “interfacial control” paradigm wherein gel-like stabilization for proppant transport is achieved via interfacial viscoelasticity rather than bulk polymer gelation, thereby directly addressing the critical imperative to harmonize fracture conductivity with reservoir protection in unconventional energy development. The findings are validated for shallow CBM reservoir conditions (25–35 °C), with extension to higher-temperature formations identified as a priority for future investigation. Full article

This study investigates spherical methyl silicone resin, a potentially environmentally friendly additive free of sulfur, phosphorus, and chlorine, as a lubricant additive in polyethylene glycol 200 (PEG 200) base oils. We evaluated concentration-response characteristics and tribological performance across PEG base oils containing 0.01–0.05 wt% resin. Tribological testing was conducted with a four-ball wear tester at 98 N and 1450 rpm for 30 min. All tested concentrations demonstrated excellent friction-reduction and anti-wear performance, with an optimal efficacy observed at 0.02 wt%. Surface characterization was performed using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. This friction-reducing and anti-wear performance is attributed to the formation of silicon-oxygen species and graphene-like carbon structures, thereby effectively suppressing direct surface contact and mitigating wear. Consequently, spherical methyl silicone resin demonstrates considerable potential as a green lubricant additive for bearing steel applications. Full article

Localized surface plasmon resonance (LSPR) is an optical phenomenon that occurs when light interacts with free electrons on the surface of metallic thin films, producing intensified electromagnetic fields at specific sites, often called “hot spots”. LSPR-based sensing technologies respond to chemical and associated optical interfacial changes. Inherent advantages include enhanced sensitivity, compact size, low production cost, and strong potential for integration into portable, point-of-care diagnostic systems. This study focuses on a detailed investigation into the surface functionalization of localized surface plasmon resonance (LSPR)-based nanohole array (NHA) sensors for biomedical applications. Gold-coated NHA surfaces were functionalized using polyethylene glycol (PEG) self-assembled monolayers (SAMs), enabling specific attachment of biomolecular species. As a proof-of-concept, bovine serum albumin (BSA) and SARS-CoV-2 nanobody proteins were successfully immobilized on the PEGylated surfaces. Individual steps of surface modification including PEGylation, protein immobilization and nanobody immobilization were validated through a dual-method approach which combined measurement of LSPR optical spectral shifts and x-ray photoelectron spectroscopy (XPS) chemical analyses. Reproducibility was assessed across multiple sensors and repeated trials, confirming the repeatability of each functionalization and binding process. The sensor system, consisting of NHA-based plasmonic platform, microfluidics, and a portable optical spectrometer, exhibits the capability for reliable and sensitive, label-free detection of biomolecular targets, including viral antigens, in liquid-phase environments. Full article

This study evaluated the effects of polyethylene glycol concentrations in enhancing the physiological performance of the rice varieties and their recovery ability after drought stress. The experiment comprised of IR64, NIL-SUB1DRO1, and NILDRO1. Seed priming was conducted by submerging 5 g of samples in petri dishes containing 100 mL of 5% and 10% PEG solutions. Drought stress significantly reduced all the growth traits, with the susceptible genotypes IR64 recorded highest reduction of shoot length 36%, tiller number 41.3%, shoot dry weight 77%, and root dry weight 72% compared to non-primed NILDRO1 and NIL-SUB1DRO1 with reduction in shoot length 34–35%, tiller number 34–45%, root dry weight 60–66%, and shoot dry weight (70–71%). Similar results were recorded for IR64, Pn, 63%, gs 78% E 66%, and RWC 66%, respectively, compared with NILDRO1 (55%, 60%, and 58%), while NIL-SUB1DRO1 showed reductions of 55%, 50%, and 54%. PEG 5% and 10% significantly enhanced primed IR64 Pn (29–57%), gs (70%), E (56–64%), and RWC 65%. During the recovery phase, primed seedlings showed a more rapid restoration of growth and photosynthetic efficiency than the non-primed seedlings. PEG 5% and 10% were effective in mitigating drought stress and enhanced recovery ability of rice. Full article

Background: Hot-melt extrusion (HME) is a promising technology for the manufacturing of drug products; however, its application is limited by elevated thermal and shear stresses that may induce degradation of thermolabile active pharmaceutical ingredients. One of the approaches to reducing processing temperatures is the use of polymeric systems with tailored thermal and rheological properties. The aim of the study was to develop an approach for the design of polymeric systems exhibiting a transient plasticization window, enabling a reduction in melt viscosity and improved processability under low-temperature extrusion conditions, followed by the formation of a structurally coherent matrix upon cooling. Methods: The compatibility of the initial polymers was assessed using laser microinterferometry. Based on the obtained data, three- and four-component polymeric compositions were designed and prepared by hot-melt extrusion. The resulting materials were characterized by differential scanning calorimetry, melt rheology analysis, and storage stability assessment. Thermal and rheological data were used to iteratively optimize the polymeric systems. Results: A four-component polymeric system based on PVP K-29/32, PEG 400, PEG 1500, and HPC EF was developed, suitable for processing by hot-melt extrusion at 70 °C. The final system enabled formation of a homogeneous extrudate, exhibited reproducible rheological behavior, and remained stable in the solid-state during storage, with no evidence of cold flow. Conclusions: It was established that, in the design of polymeric systems for hot-melt extrusion, the key factor is not achieving the lowest possible glass transition temperature, but rather the design of a system in which viscosity is transiently reduced under processing conditions and followed by structural stabilization upon cooling. The proposed approach may be applied in the development of polymeric premixes for the preparation of dosage forms by hot-melt extrusion, including those incorporating thermolabile active pharmaceutical ingredients. Full article

Hierarchical functionalisation of the UiO-66(Zr)-NH₂ metal–organic framework with cysteine, poly(ethylene glycol) (PEG), and the SARS-CoV-2 spike receptor-binding domain (RBD) was developed to enable receptor-specific interaction with the angiotensin-converting enzyme 2 receptor (ACE2) in model cells. Post-synthetic modification using cysteine and heterobifunctional PEG linkers allowed controlled bioconjugation of SpyTag-labelled RBD via SpyTag/SpyCatcher chemistry, while preserving the crystallinity, microporosity, and intrinsic optical properties of the UiO-66(Zr)-NH₂ framework. Comprehensive physicochemical characterisation confirmed successful surface functionalisation, tunable aggregation behaviour, and retention of multimodal optical characteristics. Cellular studies in HEK293T and HeLa cells overexpressing EGFP-tagged ACE2 demonstrated enhanced and selective association and uptake of RBD-functionalised nanoparticles compared with non-targeted analogues. Multimodal fluorescence imaging, fluorescence lifetime imaging microscopy, flow-cytometry, and electron microscopy indicated ACE2-dependent endocytic internalisation, with predominant localisation in endosomal and autophagosomal compartments, while both amine- and cysteine-modified formulations exhibited good biocompatibility. Overall, this study establishes a virus-mimetic, ACE2-targeted UiO-66(Zr)-based nanosystem as a proof-of-concept biointerface platform for receptor-specific cellular delivery and imaging, providing a foundation for future MOF-based nanocarriers exploiting ligand–receptor interactions. Full article

Autoimmune diseases are characterized by chronic inflammation, immune dysregulation, and excessive oxidative stress, which collectively contribute to a progressive tissue damage and organ dysfunction. Although conventional immunosuppressive and anti-inflammatory therapies remain the main therapeutic approach, their clinical efficacy is often limited by poor pharmacokinetic properties, low tissue selectivity, systemic toxicity, and adverse effects following long-term administration. In this context, antioxidant-based nanoformulations have emerged as promising multi-target therapeutic strategies for the modulation of oxidative and inflammatory pathways involved in autoimmune disorders. This review focuses on polymeric and non-polymeric nanoformulations designed to improve the solubility, stability, bioavailability, controlled release, and targeted delivery of antioxidant and anti-inflammatory agents for autoimmune disease treatment. Recent advances in nanocarrier systems applications, including nanogels, poly(lactic-co-glycolic acid) (PLGA), polyethylene glycol (PEG), polymethacrylate, chitosan, hyaluronic acid, hydroxyapatite (HAP), lipid-based and ROS-responsive nanosystems, are discussed. The therapeutic potential of nanoencapsulated steroidal and non-steroidal anti-inflammatory drugs, antioxidant compounds, enzymes, inorganic elements, and nucleic acid-binding systems is evaluated through preclinical and limited clinical evidence. Many of these reported nanoformulations exhibit enhanced therapeutic efficacy, improved tissue targeting, reduced systemic toxicity, and the ability to simultaneously modulate oxidative stress and inflammatory signaling pathways. Despite the encouraging findings, important challenges remain regarding clinical translation, long-term safety, reproducibility, and large-scale production. In overall, antioxidant nanoformulations represent a promising and evolving platform for the development of more effective and targeted therapies against autoimmune diseases. Full article

Background: Traumatic brain injury (TBI) affects millions of individuals annually and remains a major global cause of neurological disability and death. Tau protein hyperphosphorylation, particularly in its cis conformation, is a major pathological hallmark contributing to neurodegeneration following TBI. Single-chain variable fragments (scFvs), despite their diagnostic potential, suffer from rapid renal clearance and short circulation half-lives, which limit their in vivo performance. PEGylation is therefore employed to prolong systemic circulation and improve the pharmacokinetic behavior of scFvs, enabling more effective brain retention and target engagement. Methods: In this study, we utilized a previously validated anti-cis p-tau scFv antibody fragment, radiolabeled with technetium-99m tricarbonyl (^99mTc(CO)₃), as a diagnostic tracer to detect tau pathology in TBI rat models. The antibody was conjugated with polyethylene glycol (PEG, 20 kDa); PEGylation efficiency was determined by quantifying the products on SDS-PAGE, and the products were subsequently radiolabeled. Results: Radiochemical purity (RCP) was ~95.4% for the non-PEGylated tracer (^99mTc-AININ20) and ~92.7% for the PEGylated form (^99mTc-AININ20-PEG), with both showing >90% radiochemical purity consistently. Upon systemic administration, PEGylated scFv was able to cross the blood–brain barrier (BBB) and selectively accumulated in injured regions, as confirmed by single-photon emission computed tomography (SPECT) imaging. Both PEGylated and non-PEGylated scFv tracers showed significantly higher brain uptake in TBI rats compared to healthy controls (p < 0.0001). At 24 h, the PEGylated form exhibited a significantly higher brain signal than the non-PEGylated version (p < 0.0001), indicating improved tracer retention. Biodistribution analysis at 2 h post-injection showed significantly reduced renal clearance for the PEGylated tracer and increased hepatic uptake compared to the non-PEGylated form. At 24 h, in vivo imaging confirmed sustained brain retention, highlighting improved pharmacokinetics and imaging potential. Conclusions: These results support PEGylated scFv as a promising SPECT imaging agent for early detection of tauopathy in TBI, offering enhanced brain retention and improved pharmacokinetics. Full article