Search Results (267)

High Mobility Group Box 1 (HMGB1) is a central pro-inflammatory mediator released from damaged or stressed cells, where it activates receptors such as the Receptor for Advanced Glycation Endproducts (RAGE). Dendritic polyglycerol sulfate (dPGS), a hyperbranched polyanionic polymer, is known for its anti-inflammatory activity. In this study, we examined how dPGS modulates HMGB1-driven signaling in RAW 264.7 macrophages and human microglia. Recombinant human HMGB1 expressed in Escherichia coli (E. coli) was purified by nickel-nitrilotriacetic acid (Ni-NTA) and heparin chromatography. Proximity ligation assays (PLA) revealed that dPGS significantly disrupted HMGB1/RAGE interactions, particularly under lipopolysaccharide (LPS) stimulation, thereby reducing inflammatory signaling complex formation. This correlated with reduced activation of the nuclear factor kappa B (NF-κB) pathway, demonstrated by decreased nuclear translocation and transcriptional activity. Reverse transcription polymerase chain reaction (RT-PCR) and quantitative real-time PCR (RT-qPCR) showed that dPGS suppressed HMGB1- and LPS-induced transcription of tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS). Enzyme-linked immunosorbent assay (ELISA) and Griess assays confirmed reduced TNF-α secretion and nitric oxide production. Electron paramagnetic resonance (EPR) spectroscopy further showed that dPGS altered HMGB1/soluble RAGE (sRAGE) complex dynamics, providing mechanistic insight into its receptor-disruptive action. Full article

The self-consistent field Poisson–Boltzmann framework is applied for analysis of equilibrium partitioning of ampholytic protein-like nanocolloids between buffer solution and weak (pH-sensitive) versus strong polyelectrolyte (polyanionic) brushes with the same net charge per unit area. The position-dependent nanocolloid net charge and the insertion freeenergy profiles are derived as a function of pH and ionic strength in the solution. It is demonstrated that, similar to strong polyelectrolyte brushes, pH-sensitive brushes are capable of the uptake of nanocolloids in the vicinity of the isoelectric point, that is, when the net charge of the colloid in the buffer has either the opposite or the same sign as the ionized monomer units of the brush. At $pI\ge p{K}_{brush}$ and $pH\ge pI$, the particle absorption patterns by similarly (negatively) charged brushes are qualitatively similar in the cases of strong and weak polyelectrolyte brushes, but the freeenergy barrier at the brush periphery is wider for weak than for strong polyelectrolyte brushes, which may cause stronger kinetic hindrance for the nanocolloid uptake by the brush. A decrease in $pH$ below the IEP leads to a monotonic increase in the depth of the insertion freeenergy minimum inside a strong polyelectrolyte brush, whereas for weak polyelectrolyte brushes, a more peculiar trend is predicted: due to competition between the increasing positive charge of the nanocolloid and the decreasing magnitude of the negative charge of the brush, the absorption is weakened at low $pH$. Full article

Background/Objectives. Efficient nucleic acid delivery into target cells remains a critical challenge in gene therapy. Due to its advantages in biocompatibility and safety, recent research has increasingly focused on non-viral gene delivery. Methods. A series of copolymers—synthesized by integrating thermally sensitive poly(N-isopropylacrylamide) (PNIPAm), hydrophilic poly(ethylene glycol) (PEG) grafts, and a polycationic poly(L-lysine) (PLL) block of varying lengths ((PNIPAm)₇₇-graft-(PEG)₉-block-(PLL)_z, z = 10–65)—were investigated. Plasmid DNA complexation with the copolymers was achieved through temperature-modulated methods. The resulting polyplexes were characterized by evaluating complex strength, particle size, zeta potential, plasmid DNA loading capacity, resistance to anionic stress, stability in serum, and lysosomal membrane destabilization assay. The copolymers’ potential for plasmid DNA delivery was assessed through cytotoxicity and transfection studies in cancer cell lines. Results. Across all complexation methods, the copolymers effectively condensed plasmid DNA into stable polyplexes. Particle sizes (60–90 nm) ranged with no apparent correlation to copolymer type, complexation method, or N/P ratio, whereas zeta potentials (+10–+20 mV) and resistance to polyanionic stress were dependent on the PLL length and N/P ratio. Cytotoxicity analysis revealed a direct correlation between PLL chain length and cell viability, with all copolymers demonstrating minimal cytotoxicity at concentrations required for efficient transfection. PNL-20 ((PNIPAm)₇₇-graft-(PEG)₉-block-(PLL)₂₀) exhibited the highest transfection efficiency among the tested formulations while maintaining low cytotoxicity. Conclusions. The study highlights the promising potential of (PNIPAm)₇₇-graft-(PEG)₉-block-(PLL)_z copolymers for effective plasmid DNA delivery to cancer cells. It reveals the importance of attaining the right balance between polyplex tightness and plasmid release to achieve improved biocompatibility and transfection efficiency. Full article

This review examines sustainable cascading biorefinery strategies for the green alga Ulva, which is globally prevalent in eutrophic marine waters and often forms extensive “green tides.” These blooms cause substantial environmental and economic damage to coastal communities. The primary target products within an Ulva biorefinery typically encompass salts, lipids, proteins, cellulose, and ulvan. Each of these components possesses unique properties and diverse applications, contributing to the economic robustness of the biorefinery. Salts can be repurposed for agricultural or even human consumption. Lipids offer high-value applications in nutraceuticals and animal feed. Proteins present significant potential as plant-based nutritional supplements. Cellulose can be transformed into various advanced materials. Finally, ulvan, a polyanionic oligosaccharide unique to Ulva, holds promise due to its distinct properties, particularly in the biomedical field. Furthermore, state-of-the-art chemical modifications of ulvan are presented with the aim of tailoring its properties and broadening its potential applications. Future research should prioritize optimizing these integrated extraction and fractionation processes. Furthermore, a multi-product biorefining approach, integrated with robust Life Cycle Assessment studies, is vital for transforming this environmental challenge into a significant opportunity for sustainable resource valorization and economic growth. Full article

The design of high-performance drilling fluid systems is of vital importance for the safe and efficient exploitation of natural gas hydrates. Incorporating appropriate nanoparticles into drilling fluids can significantly enhance drilling fluid loss control, wellbore stability, and hydrate inhibition. However, the combined effects of nanoparticles and conventional additives on hydrate inhibition in drilling fluid systems remain poorly understood. In this study, the influence of nanoparticles on hydrate formation was first evaluated in a base mud, followed by an investigation of their combined effects with common drilling fluid additives. The results demonstrate that hydrophilic nano-CaCO₃ particles exhibit hydrate inhibitory effects, with the strongest inhibition observed at 3.0%. Composite system tests (incorporating nanoparticles with sepiolite, filtrate reducers, and flow modifiers) revealed diverse effects on hydrate formation. Specifically, the combination of nanoparticles and sepiolite promoted hydrate formation; the combination of nanoparticles and filtrate reducers showed divergent effects. Mixtures of nanoparticles with 0.2% low-viscosity anionic cellulose (LV-PAC), carboxymethyl starch (CMS), and low-viscosity carboxymethyl cellulose (LV-CMC) inhibited hydrate formation, while mixtures with 0.2% sulfonated phenolic resin (SMP-2) and hydrolyzed ammonium polyacrylonitrile (NH₄-HPAN) accelerated hydrate formation. Notably, the incorporation of nanoparticles with 0.3% guar gum, sesbania gum, high-viscosity carboxymethyl cellulose (HV-CMC), or high-viscosity polyanionic cellulose (HV-PAC) resulted in the complete inhibition of hydrate formation. By contrast, the synergistic inhibition effect of the nanoparticle/xanthan gum (XC) composite system was relatively weak, with the optimal compounding concentration determined to be 0.3%. These findings provide critical insights for the development of drilling fluid systems in natural gas hydrate reservoirs, facilitating the optimization of drilling performance and enhancing operational safety in hydrate-bearing formations. Full article

Bladder cancer remains a significant global health challenge, necessitating innovative therapeutic strategies to enhance treatment efficacy. This study investigates the potential of chitosan nanoparticles as a drug delivery system, using ciprofloxacin as a model compound and utilizing a 3D spheroid model of bladder cancer that better reflects in vivo tumour conditions. The encapsulation efficiency of ciprofloxacin was optimized on the appropriate mass ratio of chitosan to cross-linking tripolyphosphate (TPP) polyanion. The resulting spherical chitosan nanocapsules loaded with ciprofloxacin demonstrated improved stability and controlled drug release, addressing the limitations of non-encapsulated ciprofloxacin. In 3D T24 bladder cancer spheroids, encapsulated ciprofloxacin exhibited enhanced cytotoxicity compared to free-drug formulations, with significant effects observed at ciprofloxacin concentrations of 500 and 1000 μM after 48 and 72 h of exposure. The 3D spheroid model, which better mimics the tumour microenvironment than 2D cultures, enabled a more accurate drug efficacy evaluation. The results demonstrate that chitosan nanocapsules can improve the delivery and cytotoxic profile of ciprofloxacin in vitro, indicating their potential for further development as carriers in localized bladder cancer treatment. Full article

The proteolytic processing of the SARS-CoV-2 spike glycoprotein by host cell membrane-associated proteases is a key step in both the entry of the invading virus into the cell and the release of the newly generated viral particles from the infected cell. Because of the critical importance of this step for the viral infectivity cycle, it has been a target of extensive efforts aimed at identifying highly specific protease inhibitors as potential antiviral agents. An alternative strategy to disrupt the pre-fusioviden processing of the SARS-CoV-2 S glycoprotein aims to protect the substrate rather than directly inhibit the proteases. In this work, we focused on furin, a serine protease located primarily in the Golgi apparatus, but also present on the cell membrane. Its cleavage site within the S glycoprotein is located within the stalk region of the latter and comprises an arginine-rich segment (SPRRARS), which fits the definition of the Cardin–Weintraub glycosaminoglycan recognition motif. Native mass spectrometry (MS) measurements confirmed the binding of a hexadecameric peptide representing the loop region at the S1/S2 interface and incorporating the furin cleavage site (FCS) to heparin fragments of various lengths, as well as unfractionated heparin (UFH), although at the physiological ionic strength, only UFH remains tightly bound to the FCS. The direct LC/MS monitoring of FCS digestion with furin revealed a significant impact of both heparin fragments and UFH on the proteolysis kinetics, although only the latter had IC50 values that could be considered physiologically relevant (0.6 ± 0.1 mg/mL). The results of this work highlight the importance of the long-range and relatively non-specific electrostatic interactions in modulating physiological and pathological processes and emphasize the multi-faceted role played by heparin in managing coronavirus infections. Full article

Nowadays, some amorphous and microcrystalline solid-state electrolytes (SSEs) with dual anions have attained high ionic conductivity and good compatibility with electrodes in all-solid-state lithium-ion batteries (ASSLIBs). In this work, crystalline SSEs of series A (Li_1+xTaO_1+xCl_4−x, −0.70 ≤ x ≤ 0.50) and B (LiTaO_2+yCl_2−2y, −1.22 ≤ y ≤ 0), having great application potential well over ambient temperatures, were prepared at 260–460 °C for 2–10 h using Li₂O, TaCl₅, and LiTaO₃ as the raw materials. The three-phase coexisting samples attained high σ values ranging from 5.20 to 7.35 mS cm⁻¹, which are among the reported high values of amorphous co-essential SSEs and other alloplasmatic crystalline ones. It is attributed to the synergistic effect of the polyanion trans-[O₂Cl₄] and cis-[O₄Cl₂] octahedra framework. Full article

Sodium-ion batteries (SIBs) share similar working principles with lithium-ion batteries while demonstrating cost advantages. However, the current understanding of their safety characteristics remains insufficient, and the thermal runaway mechanisms of different SIB systems have not been fully elucidated. This study investigated the following two mainstream sodium-ion battery systems: polyanion-type compound (PAC) and layered transition metal oxide (TMO) cathodes. Differential scanning calorimetry (DSC) was employed to evaluate the thermal stability of cathodes and anodes, examining the effects of state of charge (SOC), cycling, and overcharging on electrode thermal stability. The thermal stability of electrolytes with different compositions was also characterized and analyzed. Additionally, adiabatic thermal runaway tests were conducted using an accelerating rate calorimeter (ARC) to explore temperature–voltage evolution patterns and temperature rise rates. The study systematically investigated heat-generating reactions during various thermal runaway stages and conducted a comparative analysis of the thermal runaway characteristics between these two battery systems. Full article

Lithium-ion batteries (LIBs) with high power, high capacity, and support for fast charging are increasingly favored by consumers. As a commercial electrode material for power batteries, LiFePO₄ was limited from further wide application due to its low conductivity and lithium-ion diffusion rate. The development of advanced architectures integrating rational conductive networks with optimized ion transport pathways represents a critical frontier in optimizing the performance of cathode materials. In this paper, a novel self-supporting cathode material (designated as LFP@LVP-CES) was synthesized through an integrated coaxial electrospinning and controlled pyrolysis strategy. This methodology directly converts LiFePO₄, Li₃V₂(PO₄)₃, and polyacrylonitrile (PAN)) into flexible, binder-free cathodes with a hierarchical structural organization. The 3D carbon nanofiber (CNF) matrix synergistically integrates LiFePO₄ (Li/Fe/PO_x) and Li₃V₂(PO₄)₃ (Li/V/PO_x) nanoparticles, where CNFs act as a conductive scaffold to enhance electron transport, while the PO_x polyanionic frameworks stabilize Li⁺ diffusion pathways. Morphological characterizations (SEM and TEM) revealed a 3D cross-connected carbon nanofiber matrix (diameter: 250 ± 50 nm) uniformly embedded with active material particles. Electrochemical evaluations demonstrated that the LFP@LVP-CES cathode delivers an initial specific capacity of 165 mAh·g⁻¹ at 0.1 C, maintaining 80 mAh·g⁻¹ at 5 C. Notably, the material exhibited exceptional rate capability and cycling stability, demonstrating a 96% capacity recovery after high-rate cycling upon returning to 0.1 C, along with 97% capacity retention over 200 cycles at 1 C. Detailed kinetic analysis through EIS revealed significantly reduced R_ct and increased Li⁺ diffusion. This superior electrochemical performance can be attributed to the synergistic effects between the 3D conductive network architecture and dual active materials. Compared with traditional coating processes and high-temperature calcination, the preparation of controllable electrospinning and low-temperature pyrolysis to some extent avoid the introduction of harmful substances and reduce raw material consumption and carbon emissions. This original integration strategy establishes a paradigm for designing freestanding electrode architectures through 3D structural design combined with a bimodal active material, providing critical insights for next-generation energy storage systems. Full article

Hydrogels (HDs) offer a promising platform for localized and sustained drug delivery. In this study, carboxymethyl chitosan (CMC)—based hydrogels were crosslinked with genipin and evaluated for the controlled release and tissue retention of suramin, a polyanionic drug with anti-inflammatory and antifibrotic properties. The influence of crosslinking density (1%, 3%, and 5%) on drug release, permeation kinetics, and retention was investigated using in vitro synthetic membranes and reconstructed human epithelial tissue models. The 1% genipin HD exhibited the highest cumulative release and drug retention (48.8 ± 6.8 μg/cm² in synthetic membranes; 24.06 ± 7.33 μg/cm² in epithelial models), along with a sustained release profile governed by first-order and Fickian diffusion kinetics. Notably, the 1% crosslinked formulation also demonstrated enhanced transmembrane flux (>140 μg/cm²/h after six hours), suggesting that lower crosslinking density favors both diffusional mobility and depot functionality. In contrast, free suramin solution displayed limited tissue interaction and minimal permeation, highlighting the role of the hydrogel matrix in regulating local bioavailability. These findings demonstrate that CMC–genipin HD can closely modulate drug delivery kinetics through crosslinking density, offering a biocompatible strategy for localized treatment of ulcerated epithelial conditions such as oral mucositis or chronic wounds. Diffusion models included a synthetic multilayer membrane (Strat-M^®) and a reconstructed human epidermis (EpiDerm™) to simulate skin-like barrier properties. Full article

Na₄Fe₃(PO₄)₂P₂O₇ (NFPP) is recognized as a prospective electrode for sodium-ion batteries (SIBs) because of its structure stability, economic viability and environmental friendliness. Nevertheless, its commercialization is constrained by low operating voltage and limited theoretical capacity, which result in a power density significantly inferior to that of LiFePO₄. To address these limitations, in this work, we first designed and synthesized a series of Mn-doped NFPP to enhance its operating voltage, inspired by the successful design of LiFe_1-xMn_xPO₄ cathodes. This approach was implemented to enhance the operating voltage of the material. Subsequently, the optimized Na₄Fe_1.2Mn_1.8(PO₄)₂P₂O₇ (1.8Mn-NFMPP) sample was selected for further Ti-doped modification to enhance its cycle durability and rate performance. The final Mn/Ti co-doped Na₄Fe_1.2Mn_1.7Ti_0.1(PO₄)₂P₂O₇ (0.1Ti-NFMTPP) material exhibited a high operating voltage of ~3.6 V (vs. Na⁺/Na) in a half cell, with an outstanding reversible capacity of 122.9 mAh g⁻¹ at 0.1 C and remained at 90.6% capacity retention after 100 cycles at 0.5 C. When assembled into a coin-type full cell employing a commercial hard carbon anode, the optimized cathode material exhibited an initial capacity of 101.7 mAh g⁻¹, retaining 86.9% capacity retention over 50 cycles at 0.1 C. These results illustrated that optimal Mn/Ti co-doping is an effective methodology to boost the electrochemical behavior of NFPP materials, achieving mitigation of the Jahn–Teller effect on the Mn³⁺ and Mn dissolution problem, thereby significantly improving structural stability and cycling performance. Full article

The sustainable production of carbon-free fuels such as hydrogen is an important goal in the search for alternative energy sources. Herein, we report a peptide-based system for light-driven hydrogen evolution from water under neutral conditions. The M1 peptide is an ABC triblock polymer featuring two coiled-coil alpha-helical regions flanking a water-soluble, polyanionic, intrinsically disordered region. M1 formed a hydrogel at high concentrations upon binding to cobalt protoporphyrin IX. This process is driven by the terminal regions, which coordinate the metalloporphyrin through histidine residues and form helical oligomers interconnected by flexible, intrinsically disordered regions, resulting in network formation. Co-M1 catalyzes hydrogen production upon irradiation in the presence of a photosensitizer and a sacrificial electron donor; the activity of Co-M1 is eight times higher than that of free Co-PPIX. Full article

Humidity sensors are widely utilized in meteorological research, industrial production, precision instrument maintenance, agriculture, health care, and other fields. However, the long response time and low sensitivity of current metal oxide and hybrid humidity sensors limit their practical applications. In this study, a humidity sensor was prepared using a simple drop-casting method with 2-hydroxy-2-methylpropiophenone (HOMPP) and 1-vinyl-3-butylimidazolium bromide (C₉H₁₅BrN₂) as the humidity sensing materials. This approach offers advantages such as low cost, high chemisorption capacity, and excellent moisture-sensitive performance. The prepared humidity sensors demonstrate high sensitivity, good repeatability, excellent flexibility, low hysteresis, and response/recovery times of 6/12.5 s, respectively, over a wide relative humidity (RH) range (2–97%). Additionally, the sensor exhibits potential for various multifunctional applications, including humidity detection in daily life, respiratory monitoring, non-contact sensing, and flexible electronics applications. Full article

Herein, we investigate the performance and safety of four of the early-stage, commercial Na-ion batteries available in 2024, representing the most popular cathode types across research and commercialization: polyanion (Na-VPF), layered metal oxide (Na-NMF), and a Prussian blue analog (Na-tmCN). The cells deliver a wide range of energy density with Na-tmCN delivering the least (23 Wh/kg) and Na-NMF delivering the most (127 Wh/kg). The Na-VPF cell was in between (47 Wg/kg). Capacity retention under specified cycling conditions and with periodic 0 V excursions was the most robust for the Na-tmCN cells in both cases. Accelerating rate calorimetry (ARC) and nail penetration testing finds that Na-NMF cells do undergo thermal runaway in response to abuse, while the Na-VPF and Na-tmCN exhibit only low self-heating rates (<1 °C/min). During these safety tests, all cells exhibited off-gassing, so we conducted in-line FTIR equipped with a heated gas cell to detect CO, CO₂, CH₄, toxic acid gases (HCN, HF, NH₃), and typical electrolyte components (carbonate ester solvents). Gases similar to those detected during Li-ion failures were found in addition to HCN for the Na-tmCN cell. Our work compares different types of commercial Na-ion batteries for the first time, allowing for a more holistic comparison of the safety and performance tradeoffs for different Na-ion cathode types emerging in 2024. Full article