Search Results (23,508)

Hypertension and chronic kidney disease (CKD) are closely linked conditions and represent common global health problems. Hypertension is a leading risk factor for cardiovascular disease, which is the main cause of mortality in CKD. Endothelial injury underlies the etiopathogenesis of both hypertension and CKD. The endothelial glycocalyx (eGC) is a dynamic, negatively charged, carbohydrate-rich layer that covers the luminal surface of endothelial cells. Its primary physiological function is to protect the endothelium, including the regulation of vascular permeability and homeostasis. Damage to the eGC, known as “shedding”, is an early predictor of endothelial dysfunction and is driven by oxidative stress and low-grade inflammation. In hypertension, loss of eGC integrity—often impaired by a high-salt diet—can reduce the bioavailability of nitric oxide (NO) and increase arterial stiffness. Similarly, in CKD, uremic toxicity, hypertension, and inflammation damage the eGC, resulting in increased permeability, albuminuria, and higher cardiovascular risk. This review summarizes current evidence and underscores the potential of eGC shedding markers, especially syndecan 1 (SDC-1) and hyaluronic acid (HA), as early predictors of vascular risk and disease progression in hypertension and CKD. Full article

This study focused on elucidating the effects of chitosan (Ch), hyaluronic acid (HA), and titanium dioxide nanoparticles (nano-TiO₂) on the physicochemical characteristics of a model bacterial membrane (layer) composed of the phospholipid DPPG (1,2-dipalmitoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt). The membrane was prepared on mica using the Langmuir–Blodgett (LB) technique from an aqueous subphase containing Ch, HA and/or TiO₂. Its surface properties were subsequently characterized by optical profilometry and surface free energy estimation. The nanoscale topography of the DPPG layer provided a biomimetic platform that reflects the organization of bacterial membranes, enabling a precise evaluation of how external agents, such as Ch, HA, and nano-TiO₂, modify the surface’s structural and energetic properties. The results showed that the LB films exhibit mildly heterogeneous topography, which can be attributed to lipid domains with distinct molecular packing densities. Depending on the type of biopolymer employed with TiO₂, distinct topographic architectures of the DPPG monolayers were obtained. Furthermore, the presence of nano-TiO₂ was clearly manifested as a topographic irregularity, while the analysis of hydrophilic–hydrophobic properties revealed a structurally perturbed lipid film. The results provide detailed insight into how these specific molecules (Ch, HA, nano-TiO₂) interact at the molecular level with model bacterial membranes, offering a comprehensive picture of cell–microenvironment interactions. Full article

The complex surface architecture of natural oyster reefs is widely considered to promote biological attachment, yet the underlying mechanisms and the relevance to the design of artificial reefs are not fully understood. Here, we combined field experiments, 3D surface characterization, and numerical modelling to quantify how reef-like roughness regulates biofouling development and near-wall flow around artificial substrates. Surface morphological characteristics of natural oyster reefs were first obtained by 3D scanning and used to fabricate concrete panels with simulated rough textures, while traditional smooth concrete panels served as controls. The two types of panels were simultaneously deployed in the target sea area for a hanging-panel experiment. Samples were collected after 3, 6, 9, and 12 months to track changes in biofouling communities. At each sampling time, the panel surfaces were quantified by canopy roughness ($R_C$), surface heterogeneity ($\sigma$), and fractal dimension ($D$), and these metrics were integrated into numerical simulations combined to resolve the flow field, turbulence kinetic, and near-wall shear stress around the colonized panels. The research results show that, after 12-month immersion, the mean thickness of the biofouling layer on rough and control panels reached 6.39 mm and 5.91 mm, respectively. Rough panels exhibited consistently higher $R_C$ and $\mathsf{\sigma }$ than controls, and these two parameters are strongly linearly correlated ($R^2=0.891)$. Numerical simulations reveal that increased $R_C$ enlarges the oyster settlement shear-stress window (OSSW), indicating more favorable hydrodynamic conditions for oyster settlement and growth on rough panels. Nevertheless, the hydrodynamic differences between the initial rough panels and control panels gradually diminish over time, suggesting that biological growth can progressively naturalize initially smooth substrates. These findings advance the mechanistic understanding of how small-scale roughness and biofouling co-evolve to shape oyster habitat quality and provide a quantitative basis for the eco-engineering design of artificial oyster reefs. Full article

In this study, commercial Ospray-2507 super-duplex stainless steel powder was investigated for the first time as a potential metal support material for solid oxide cells. Initially, metal supports were fabricated and processed in air using various sintering profiles, followed by comprehensive mechanical, structural and electrochemical characterization. The optimal sintering condition was identified as 900 °C for 5 h. Subsequently, sintering under a H₂ atmosphere was explored, and its effects on the microstructural and functional properties of the metal supports were systematically to assessed to evaluate the influence of the sintering atmosphere on material performance. Although X-ray diffraction patterns showed no phase changes between the two sintering atmospheres, notable improvements were observed in mechanical, electrochemical, and microstructural properties under H₂ sintering. XPS spectra reveal that both air- and hydrogen-treated surfaces remain rich in chromium (Cr) and Manganese (Mn), which together dominate the surface and consequently attenuate the signal from the underlying iron. The thickness of the Cr- and Mn-based oxide layer decreases when sintering MS in H₂ atmosphere. Specifically, mechanical strength, as measured by three-point bending tests, increased by a factor of 12.5, and hardness rose from 500.3 to 523.5 HV. Furthermore, electrical conductivity also improved significantly, exhibiting an approximately 2.3–2.4 fold increase under H₂-sintered conditions. Full article

The practical application of inorganic ferroelectric fillers in flexible piezoelectric composites is critically constrained by low polarization efficiency and severe interfacial incompatibility with polymer matrices. Herein, we report a multi-level in situ surface modification strategy that simultaneously addresses both limitations. High-purity one-dimensional tetragonal barium titanate nanofibers (BTO NFs) are first synthesized via sol–gel electrospinning combined with a two-step gradient annealing process, which precisely controls phase evolution and preserves structural continuity. To overcome the detrimental acid-induced degradation of BTO NFs during functionalization, a polydopamine (PDA) buffer layer is first conformally coated, followed by the liquid-phase deposition of a conductive polypyrrole (PPy) shell, forming a robust core–shell PPy@PBT NFs architecture. Incorporating only 4 wt% of these multifunctional fillers into a poly(vinylidene fluoride) (PVDF) matrix yields a dramatic enhancement in electromechanical performance. The resulting flexible piezoelectric energy harvesters achieve a piezoelectric coefficient (d₃₃) of 28.7 pC/N, an output voltage of 13 V, and an output current of 0.7 μA, representing substantial improvements over unmodified filler systems. This synergistic enhancement originates from the PDA-mediated interfacial stress transfer and the PPy-induced Maxwell–Wagner polarization intensification, establishing a robust and generalizable paradigm for high-performance flexible piezoelectric composites in self-powered wearable electronics. Full article

Aiming at the rain protection problem of outdoor precision instruments such as total stations, this paper designs an environmentally adaptive intelligent protection system based on D-S evidence fusion and state machine control. In terms of mechanical structure, the protective cover is designed as a sinking type, which not only improves the safety of the equipment but also avoids the shielding problem of the working surface compared with the traditional upward-lifting structure. The system collects data from multi-source meteorological sensors and uses D-S evidence theory for fusion decision-making. To alleviate decision conflicts in high-conflict scenarios, a conflict-guided dynamic weight adjustment strategy is introduced. Combined with a dual-layer finite state machine, the system realizes coordinated control between environmental perception and protection actions and can activate protection within 30 s under severe weather. Simulation results show that the improved method increases the response speed by 41.9–62.5% compared with traditional D-S fusion in weather transition conditions. In a 28-day field test, the system achieves a daily protection success rate of 96.4% and 100% reliability in critical weather transitions. The proposed system can provide reliable support for the all-weather safe operation of field precision measurement equipment. Full article

The redox mechanisms of silica-supported Ni particles were investigated using their in situ X-ray absorption fine structure, providing mechanistic insights into partially reduced NiO and partially oxidized metallic Ni. The results of surface oxidation of partially reduced NiO particles at room temperature revealed that the surface was not fully covered with metallic Ni and that metallic Ni had also formed within the particle interior. During NiO particle reduction, the process initiates at specific surface sites, and before the metallic Ni phase fully covers the surface, O²⁻ ions are expelled from the particle. Conversely, the oxidation of metallic Ni particles progresses inward from the surface, with an accompanying increase in the thickness of the NiO layer that forms upon O₂ exposure at room temperature. This mechanism is supported by observations that the reduction of a thin NiO shell on metallic Ni particles was completed below 200 °C, while reduction temperatures shifted to higher values as the NiO layer thickness increased. The distinct oxidation and reduction mechanisms are attributed to differences in the migration direction of O²⁻ ions. During reduction, it is proposed that O²⁻ ions within the particles migrate to the surface along the interface between the NiO phase and the metallic Ni phase. This study elucidates the detailed mechanism behind the redox interconversion between NiO and metallic Ni in solid catalyst particles. Full article

In this work, poly(acrylic acid)-based layers were injected to form a sandwich layer between the cationic and anionic species for a compact and effective fire-retardant coating on cotton fabric using the layer-by-layer coating technique. From the SEM analysis, as the number of tri-layers increases, the attachment intensity increases, as can be seen for poly(acrylic acid) chitosan and bentonite clay PCB-5TL (the highest tri-layers), while in the case of halloysite-based coatings, as the number of tri-layers increases, instead of attachment, the agglomeration increases due to the high surface area of halloysite nanoclay tubes. FTIR and UV confirmed the finding from the new peak entry and an increase in thickness. The highest thermal residue, ~18%, was obtained for poly(acrylic acid) chitosan and halloysite nanoclay PCH-5TL with a maximum degradation peak intensity at ~389 °C. From the flammability and after-burning SEM investigation test, it was observed that the halloysite-based coating with a higher number of layers offered higher resistance against the flame spread and ignition and, thus, produced a higher amount of char. Full article

We conducted a paired gravity and seismic survey at Kentland Crater with the goal of investigating its subsurface density structure. Our results show that the complex crater hosts a ~4.5 mGal Bouguer gravity high corresponding to the central uplift. The southeastern portion of the crater structure exhibits a low-gravity annulus at 3.5–4.5 km radius, with an adjacent high that we define as the rim at ~5.0 km radius, implying a 10 km apparent diameter. Passive seismic data is used to characterize the low-density glacial till layer, which blankets the bedrock throughout the study area. The central gravity anomaly persists after removing the gravitational influence of the till layer. Kentland’s large, positive central gravity anomaly is likely due to the removal of the low-density material beneath the original crater floor by extensive erosion via glacial scouring. We therefore suggest that the impact-induced porosity at Kentland Crater was likely confined to the original near-surface (<900 m), which aligns with recent numerical modeling. Due to the wide range of diameter estimates, we conclude that the current geometry of Kentland Crater remains ill-defined. Compiled datasets are provided here for use in future investigations. Full article

Soil salinity poses a major challenge to agricultural productivity, especially threatening food security in arid and semi-arid areas. Traditional soil reclamation methods, such as leaching, chemical amendments, and drainage engineering, usually need large amounts of water, involve high costs, and can lead to environmental problems. This review compiles existing knowledge on innovative strategies for managing saline soils, focusing on buried interlayer systems that use materials like straw, sand, gravel–sand mixtures, and biochar. These interlayers improve soil hydraulic properties by preventing capillary rise, encouraging salt leaching, and reducing surface salt buildup. Biochar stands out as a particularly useful material because of its stability, large surface area, porosity, and high cation exchange capacity. These features help improve soil structure, increase water retention, and effectively retain sodium. Evidence from lab and field tests shows that buried biochar layers can stop salt from moving upward, aid in desalinating the root zone, and boost crop yields. While straw and sand interlayers show potential in reducing salinity, biochar is noted for its multifunctionality and long-term effectiveness in addressing salinity problems. The success of buried biochar systems depends on several factors, including the properties of the biochar, how much is used, how deep it is buried, and the specific soil and climate conditions. This review highlights how these systems work, compares their performance, and points out research gaps, advocating for their potential as a sustainable, resource-efficient way to manage salinity and improve soil health over the long term. A substantial proportion of the existing evidence is derived from controlled laboratory studies, and the buried biochar layer approach remains an emerging technique that requires further validation under field conditions. Still, significant knowledge gaps persist regarding long-term performance and water-salt dynamics, while site-specific soil variability and scalability challenges may limit the effective implementation of biochar interlayer systems under field conditions. Full article

Advances in dental material science over recent decades have significantly improved the mechanical, physical, esthetic, and adhesive properties of restorative systems. As clinical performance and durability have reached high standards, research has progressively shifted from purely mechanical replacement toward the development of bioactive materials capable of interacting beneficially with biological tissues. Rather than functioning solely as passive restoratives, contemporary materials are increasingly designed to contribute to disease prevention and tissue repair. Bioactive functionality encompasses both bioprotective and biopromotive effects, including antimicrobial activity, reinforcement of the dental substrate, promotion of remineralization, modulation of inflammatory responses, and stimulation of regenerative pathways. In this context, the surface pre-reacted glass ionomer (S-PRG) particle has emerged as a multifunctional bioactive technology. Its unique three-layer structure enables sustained release of multiple ions, fluoride, strontium, boron, sodium, silicate, and aluminum, associated with mineralization, biofilm inhibition, inflammatory regulation, and activation of cellular signaling pathways. An integrative review was conducted through a literature search in PubMed, SciELO and Scopus using the descriptors “Surface-reaction-type prereacted glass ionomer” and “S-PRG.” Experimental studies evaluating antimicrobial, anti-inflammatory, remineralizing, cellular, or regenerative effects of S-PRG-containing materials were considered eligible. A total of 49 studies met the inclusion criteria and were analyzed through descriptive synthesis. The available evidence indicates that the biological activity of S-PRG-containing materials extends beyond caries prevention, including modulation of inflammatory responses, enhancement of mineralization processes, and stimulation of cellular pathways related to tissue repair. These findings highlight the potential of S-PRG technology as a promising strategy for the development of restorative materials with regenerative and preventive properties. Full article

The molecular chaperone paradigm has shaped modern views of assisted protein folding, yet it does not fully capture the physical context in which de novo folding occurs in cells. A defining feature of the cellular milieu is macromolecular tethering in cis, whereby nascent polypeptides remain physically linked—through covalent or persistent associations—to ribosomes, lipid bilayers, or pre-folded domains of multidomain proteins. Because molecular chaperones have traditionally been defined as reversible binders acting in trans, this cis-acting mode has remained conceptually underappreciated. Cellular macromolecules, by virtue of their steric bulk and surface charges, can suppress aggregation of tethered polypeptides, thereby increasing productive folding yield. By analogy to colloidal stability, this repulsion-mediated control of aggregation suggests that cellular macromolecules can exhibit intrinsic chaperone-like activity largely independent of whether the linkage occurs in cis or in trans. This property provides a conceptual basis for linking cis- and trans-acting chaperoning. Thus, macromolecular tethering in cis may constitute a built-in layer of cellular chaperoning, distinct in physical linkage yet mechanistically related to conventional molecular chaperones. Full article

Dark current represents a fundamental limiting factor in photodiode performance, establishing the noise floor and constraining detectivity in low-light applications. This comprehensive literature review examines publications covering the physical mechanisms underlying dark current generation and diverse techniques employed for its reduction. Covered mechanisms include diffusion current, Shockley–Read–Hall (SRH) generation–recombination, trap-assisted tunneling, band-to-band tunneling, and surface leakage, each examined with respect to its physical origin and characteristic signatures. Reduction strategies are categorized into thermal management approaches, surface passivation techniques including atomic-layer-deposited aluminum oxide (ALD Al₂O₃), guard ring architectures (attached, floating, and combined configurations), gettering and defect engineering methods, doping profile optimization, bias voltage management, and advanced device architectures such as pinned photodiodes and black silicon structures. A classification table organizes all the reviewed literature by material system, reduction technique, and key findings. Special emphasis is placed on silicon, germanium, III–V compounds, and emerging material photodiodes relevant to near-infrared detection, CMOS imaging, single-photon avalanche diodes (SPADs), and Time-of-Flight (ToF) applications. Full article

Silver films are key building blocks for plasmonic and nanophotonic devices, whose optical performance and device reliability are highly sensitive to particulate contamination introduced during fabrication and operation. Herein, a non-destructive surface cleaning strategy specifically applicable to silver film systems is proposed, based on the synergistic regulation of the mechanical properties of a polymer layer and its interfacial adhesion to the silver film. Such regulation is achieved by tuning hydrogen-bond-mediated interactions within a modified poly(vinyl alcohol) (PVA) layer, enabling effective control over the locus of fracture during peeling, such that fracture preferentially occurs at the polymer/silver interface. Unlike conventional polymer-assisted cleaning methods that suffer from an inherent trade-off between bulk cohesion and interfacial adhesion, this approach decouples the two properties through molecular-level hydrogen-bond redistribution. As a result, particulate contaminants can be efficiently removed from the silver surface while preserving the structural integrity of the silver film. The proposed method achieves a particle removal efficiency of up to 98% for contaminants larger than 30 nm and can be stably applied to silver films with lateral dimensions ranging from 1 inch to 12 inches, demonstrating excellent scalability. By further adjusting the processing parameters and compositional ratios of the polymer layer, this strategy is expected to be adaptable to silver films with different thicknesses and structural configurations, providing a reliable surface cleaning solution for improving the performance and reliability of plasmonic and optoelectronic thin-film devices. Full article

Pavement energy harvesting has been investigated as a means of converting traffic loading, solar radiation, and pavement thermal gradients into usable electricity or heat. This paper reviews 135 publications available through March 2026 and evaluates the field from a pavement engineering perspective. The literature is organized into six technology families: piezoelectric systems, mechanical-electromagnetic systems, triboelectric systems, thermoelectric systems, hydronic/geothermal/solar-thermal pavements, and photovoltaic or pavement-integrated photovoltaic-thermal systems. The review considers not only reported energy output, but also structural compatibility, durability, constructability, maintenance requirements, safety, and deployment conditions. The synthesis shows that the most credible near-term roles of piezoelectric and triboelectric systems are self-powered sensing and other localized low-power functions rather than bulk electricity generation. Mechanical-electromagnetic systems can produce larger event-level output, but their practicality is limited to low-speed and highly controlled settings because they rely on deliberate surface displacement. Thermoelectric systems are mechanically compatible with pavements, yet their performance remains constrained by weak and transient temperature gradients. Hydronic and solar-thermal pavements are presently the most infrastructure-compatible option for large-area energy recovery because they deliver useful heat and align with snow-melting, seasonal storage, and adjacent building-energy applications. Photovoltaic and photovoltaic-thermal pavements offer direct electrical generation, but continued challenges with transparent cover layers, surface friction, durability, fouling, and maintenance still limit broad roadway deployment. Overall, the review indicates that future progress will depend less on maximizing peak output in isolated prototypes and more on integrated pavement-energy design, standardized performance reporting, durability assessment, techno-economic evaluation, and corridor-scale demonstration. Full article