Stabilization Mechanism Research Articles

Integrating strategy to investigate the formation and stabilization mechanisms of Curcumin-Cyclodextrin inclusion complexes: experimental characterizations and multi-scale computational simulations.

The Cyclodextrin (CD) encapsulation technology can significantly enhance the water solubility of Curcumin (CUR) and effectively protect it against chemical degradations. In the current study, a combination of experimental and multi-scale computational approaches was used to investigate the binding mechanism between CUR and β-CDs (β-CD, 2-HP-β-CD, Me-β-CD, and DM-β-CD). Phase solubility studies showed that β-CDs exhibited a strong binding affinity with CUR and significantly enhanced its solubility. SEM, PXRD, DSC, and TG analysis confirmed the formation of inclusion complexes, resulting in the transition of CUR from crystalline to an amorphous state. FTIR, 1H, and 13CNMR spectra deduced that CUR may have multiple binding conformations with β-CDs. The rationality of molecular dynamics simulation systems was confirmed by comparing the simulated IR spectrum from quantum mechanics with the experimental IR spectrum. MM-PBSA and umbrella sampling simulation calculated the binding free energy of the CUR/CD inclusion complexes, ranking Me-β-CD > DM-β-CD > 2-HP-β-CD > β-CD, and clarified that van der Waals interaction played a major role in stabilizing the inclusion complexes. RDF analysis confirmed that the release of high-energy water molecules drove the formation of the CUR/CD inclusion complex, and the β-CD substituents affected their exterior hydration layer. Additionally, principal component analysis (PCA) and non-covalent interaction analysis revealed three CUR/CD binding modes: bead-on-string, terminal insertion, and V-shaped-folding. The research strategy adopted here can serve as a paradigm for investigating the encapsulation mechanism of poorly soluble drugs with CDs.

Host Material Viscoelasticity Determines Wrinkling of Fungal Films.

Microbial organisms react to their environment and are able to change it through biological and physical processes. For example, fungi exhibit various growth morphologies depending on their host material. Here, we show how the rheological properties of the host material influence the fungal wrinkling morphology. Rheological data of the host material was set in relation to the growth morphology. On host material with high storage modulus, the fungal film was flat, whereas on host material with low storage modulus, the fungus showed a morphology made of folds and wrinkles. We combined our findings with mechanical instability theories and found that the formation of wrinkles and folds is dependent on the storage modulus of the host material. The connection between the wrinkling morphology and the storage modulus of the host material is shown with simple scaling theories. The amplitude, number of wrinkles, and wrinkle length follow geometrical laws, and the mechanical properties of the fungal film are expected to increase with increasing host material elasticity. The obtained results show the connection between living biological films, how they react to their surroundings, and the underlying physical mechanisms. They can provide a framework to further design fungal materials with specific surface morphologies.

Comparison between Green and Chemical Synthesis of Silver Nanoparticles: Characterization and Antibacterial Activit

Using chemical reduction and green technology, two different approaches are used in the current work to synthesize silver nanoparticles. Pomegranate peel extract has been utilized in green technology applications. Furthermore, In the chemical approach, polyvinylpyrrolidine and ascorbic acid were utilized as reducing agents, and the optical, structural, and antibacterial characteristics of the two versions were investigated. In comparison to the chemical reduction variant (30.38 nm), the particle sizes in the green technique (19.5 nm) were smaller. Comparing green silver nanoparticles to chemically synthesized silver nanoparticles, SEM pictures showed that the former had formed a distinct crystalline shape and were evenly distributed on the surface. Granules constituted the shape of the particles. Additionally, it spreads topically. Whereas the greenly synthesized variant's absorption band was at 280 nm, the chemically synthesized variant's absorption band was at 300 nm. It was demonstrated by spectroscopic data of green silver nanoparticles that they have the capacity to produce and stabilize silver nanoparticles. Chemically produced green silver nanoparticles were also exposed to FTIR analysis to identify active functional groups. Silver particles can also be stabilized by chemically produced silver nanoparticles. To assess the antibacterial activity, the nanoparticle agar diffusion method was employed. The bacteria detected in the medium were Staphylococcus aureus and Escherichia coli. In the green form, the bacterial growth inhibition zone was larger and was produced with varying concentrations of 25 ml, 50 ml, 75 ml, and 100 ml, or 13 ml, 10 ml, 9 ml, and 8 ml for Staphylococcus aureus and 15 ml, 12 ml, 10 ml, and 7 ml for E. coli, respectively. Green-produced transcripts exhibited higher antibacterial responses, which were likely caused by the faster rate of nanoparticle stabilization mechanism by organic compounds found in pomegranate fruit peel extract.

Theoretical insights into the diverse stabilizing effects of fenchyl alcohol/thymol eutectic solvent on carotenoids

Carotenoids, a class of vital natural pigments, are known for their antioxidant properties and are integral to various industrial applications. However, their instability during processing and storage has limited their broader utilization. This study investigated the stabilizing effects of a fenchyl alcohol/thymol-based deep eutectic solvent (DES) on a spectrum of carotenoids, including lutein, zeaxanthin, astaxanthin, and β-carotene. Through a combination of ab initio molecular dynamics (AIMD) simulations and quantum chemical calculations, we elucidated the molecular interactions and stabilization mechanisms within the DES environment (methanol as the benchmark). Our findings reveal that the DES could exert varying degrees of influence on the stability of different types of carotenoids. The temperature-dependent behavior of carotenoids in the DES suggested a complex interplay between hydrogen bonding, dispersion forces, and the inherent structural properties of carotenoids. AIMD simulations provided a detailed picture of the structural organization and hydrogen bond network topology within the DES, highlighting the role of temperature on the stability and orientation of solvent molecules around carotenoids. Energy decomposition analysis (EDA), Hirshfeld surface analysis, and visual study of interactions further dissected the non-covalent interactions, emphasizing the significance of electrostatic and dispersion forces-driven non-covalent interactions (van der Waals dispersion interactions) in stabilizing carotenoids within the DES matrix. In comparison to methanol, the interactions between components of the eutectic system and the target molecules demonstrate enhanced dynamism, increased complementarity, and a greater variety of interaction patterns. This research presented a novel perspective on the use of DESs for the stabilization of carotenoids, offering potential solutions to enhance their industrial applicability and performance. The insights gained from this study are crucial for the development of sustainable and eco-friendly solvent systems, aligning with the growing demand for green chemistry in the pharmaceutical, cosmetic, and food industries.

Mechanisms of soil organic carbon and nitrogen stabilization in mineral-associated organic matter – insights from modeling in phase space

Abstract. Understanding the mechanisms of plant-derived carbon (C) and nitrogen (N) transformation and stabilization in soil is fundamental for predicting soil capacity to mitigate climate change and support other soil functions. The decomposition of plant residues and particulate organic matter (POM) contributes to the formation of mineral-associated (on average more stable) organic matter (MAOM) in soil. MAOM is formed from the binding of dissolved organic matter (ex vivo pathway) or microbial necromass and bioproducts (in vivo pathway) to minerals and metal colloids. Which of these two soil organic matter (SOM) stabilization pathways is more important and under which conditions remains an open question. To address this question, we propose a novel diagnostic model to describe C and N dynamics in MAOM as a function of the dynamics of residues and POM decomposition. Focusing on relations among soil compartments (i.e., modeling in phase space) rather than time trajectories allows isolating the fundamental processes underlying stabilization. Using this diagnostic model in combination with a database of 36 studies in which residue C and N were tracked into POM and MAOM, we found that MAOM is predominantly fueled by necromass produced by microbes decomposing residues and POM. The relevance of this in vivo pathway is higher in clayey soils but lower in C-rich soils and with N-poor added residues. Overall, our novel modeling in phase space proved to be a sound diagnostic tool for the mechanistic investigation of soil C dynamics and supported the current understanding of the critical role of both microbial transformation and mineral capacity for the stabilization of C in mineral soils.

The mitochondrial Na+/Ca2+ exchanger NCLX is implied in the activation of hypoxia-inducible factors

Eukaryotic cells and organisms depend on oxygen for basic living functions, and they display a panoply of adaptations to situations in which oxygen availability is diminished (hypoxia). A number of these responses in animals are mediated by changes in gene expression programs directed by hypoxia-inducible factors (HIFs), whose main mechanism of stabilization and functional activation in response to decreased cytosolic oxygen concentration was elucidated two decades ago. Human acute responses to hypoxia have been known for decades, although their precise molecular mechanism for oxygen sensing is not fully understood. It is already known that a redox component, linked with reactive oxygen species (ROS) production of mitochondrial origin, is implied in these responses. We have recently described a mechanism by which the mitochondrial sodium/calcium exchanger, NCLX, participates in mitochondrial electron transport chain regulation and ROS production in response to acute hypoxia.Here we show that NCLX is also implied in the response to hypoxia mediated by the HIFs. By using a NCLX inhibitor and interference RNA we show that NCLX activity is necessary for HIF-α subunits stabilization in hypoxia and for HIF-1-dependent transcriptional activity. We also show that hypoxic mitochondrial ROS production is not required for HIF-1α stabilization under all circumstances, suggesting that the basal cytosolic redox state or other mechanism(s) could be operating in the NCLX-mediated response to hypoxia that operates through HIF-α stabilization. This finding provides a link between acute and medium-term responses to hypoxia, reinforcing a central role of mitochondrial cell signalling in the response to hypoxia.

Stabilization of arsenic-cadmium co-contaminated soil with the iron-manganese sludge derived amendment: Effects and mechanisms

An iron-manganese sludge-derived amendment was proposed to remediate arsenic (As) and cadmium (Cd) co-contaminated soil, with a strong adsorptive capacity across pH 4 to 10. The Langmuir model defined maximum adsorption at 78.17 mg/g for As(III), 110.48 mg/kg for As(V), and 65.77 mg/g for Cd(II). The X-ray photoelectron spectroscopy (XPS) spectra provided insights into the chemical interactions: As was predominantly complexed or ligand exchanged with iron(hydr)oxides. In contrast, cadmium exhibited a tendency to bond with acylamino and carboxyl groups, in addition to the ferric hydroxyl groups. Notably, 42.15% of the adsorbed As(III) was oxidized into As(V) by Mn(IV) oxides present in the amendment. The soil-verification experiment demonstrated that an amendment dosage of 40 g/kg was efficacious in reducing the leaching concentration of As and Cd to maintained below the safety thresholds of 0.1 mg/L and 0.01 mg/L, respectively, for pH levels 4 to 11, meeting the Chinese Surface Water Quality Standard V (GB3838-2002). After the stabilization, the exchangeable fractions of As and the acid-soluble fractions of Cd were significantly reduced, with these elements being transformed into more stable forms. The amendment maintained the soil's neutral pH and adjusted the soil physicochemical properties. This article presents a holistic approach by examining the organic-inorganic composite of iron-manganese oxides with polyacrylamide, modified as a stabilizing amendment for As and Cd co-contaminated soil. This innovative amendment adeptly navigates the previously conflicting stabilization mechanisms for anionic and cationic metals. Offering dual advantages, the amendment not only remediates soil but also addresses the disposal of waste, presenting a win-win solution for environmental management.

Research advance on soil organic carbon stabilization mechanisms during vegetation restoration on the Loess Plateau, Northwest China.

The Loess Plateau is renowned for its deep soil layer and rich in organic carbon (C). In recent years, numerous ecological restoration projects have been undertaken on the Loess Plateau, with consequence on the stability of soil organic carbon (SOC). The SOC stability is pivotal for its capacity to sequestrate and store C. However, comprehensive review on the characteristics of SOC stability and its mechanisms during vegetation restoration on the Loess Plateau is scarce. Therefore, we summarized the dynamics of SOC stability during vegetation restoration on the Loess Plateau, discussed the mechanisms of SOC stabilization, including mineral protection, physical protection, and biological mechanisms. Furthermore, we prospected the future development directions and research focus of SOC stability research during vegetation restoration on the Loess Plateau to provide scientific support for theory and technology of soil C sequestration and stabilization during vegetation restoration, and to provide scientific reference for achieving the "double-carbon" goals.

DMD and microlens array as a switchable module for illumination angle scanning in optical diffraction tomography.

Optical diffraction tomography (ODT) enables label-free and morphological 3D imaging of biological samples using refractive-index (RI) contrast. To accomplish this, ODT systems typically capture multiple angular-specific scattering measurements, which are used to computationally reconstruct a sample's 3D RI. Standard ODT systems employ scanning mirrors to generate angular illuminations. However, scanning mirrors are limited to illuminating the sample from only one angle at a time. Furthermore, when operated at high speeds, these mirrors may exhibit mechanical instabilities that compromise image quality and measurement speed. Recently, newer ODT systems have been introduced that utilize digital-micromirror devices (DMD), spatial light modulators (SLMs), or LED arrays to achieve switchable angle-scanning with no physically-scanning components. However, these systems associate with power inefficiencies and/or spurious diffraction orders that can also limit imaging performance. In this work, we developed a novel non-interferometric ODT system that utilizes a fully switchable module for angle scanning composed of a DMD and microlens array (MLA). Compared to other switchable ODT systems, this module enables each illumination angle to be generated fully independently from every other illumination angle (i.e., no spurious diffraction orders) while also optimizing the power efficiency based on the required density of illumination angles. We validate the quantitative imaging capability of this system using calibration microspheres. We also demonstrate its capability for imaging multiple-scattering samples by imaging an early-stage zebrafish embryo.

Atomistic Insights into the Stabilization of TDP-43 Protofibrils by ATP.

The aberrant accumulation of the transactive response deoxyribonucleic acid (DNA)-binding protein of 43 kDa (TDP-43) aggregates in the cytoplasm of motor neurons is the main pathological hallmark of amyotrophic lateral sclerosis (ALS). Previous experiments reported that adenosine triphosphate (ATP), the universal energy currency for all living cells, could induce aggregation and enhance the folding of TDP-43 fibrillar aggregates. However, the significance of ATP on TDP-43 fibrillation and the mechanism behind it remain elusive. In this work, we conducted multiple atomistic molecular dynamics (MD) simulations totaling 20 μs to search the critical nucleus size of TDP-43282-360 and investigate the impact of ATP molecules on preformed protofibrils. The results reveal that the trimer is the critical nucleus for TDP-43282-360 fibril formation and the tetramer is the minimal stable nucleus. When ATP molecules bind to the TDP-43282-360 trimer and tetramer, they can consolidate the TDP-43282-360 protofibrils by increasing the content of the β-sheet structure and promoting the formation of hydrogen bonds (H-bonds). Binding site analyses show that the N-terminus of TDP-43282-360 protofibrils is the main binding site of ATP, and R293 dominates the direct binding of ATP. Further analyses reveal that the π-π, cation-π, salt bridge, and H-bonding interactions together contribute to the binding of ATP to TDP-43282-360 protofibrils. This study decoded the detailed stabilization mechanism of protofibrillar TDP-43282-360 oligomers by ATP, and may provide new avenues for the development of drug design against ALS.

Mechanisms of Pickering emulsion formation and stabilization by composite arabinoxylan–whey protein isolate particles

Few systematic studies were performed into the properties of arabinoxylan (AX) and protein composite particles, and their mechanisms of action in an emulsion remain largely unknown. In this study, composite particles based on different concentrations of AX and whey protein isolate (WPI) were constructed, and a systematic characterization was conducted to determine their functional properties. A good compatibility was found between WPI and AX, and the composites exhibited an enhanced thermal stability and consistent particle sizes. Molecular interactions, including hydrogen bonds, were detected between WPI and AX, and the composite particles containing 4% AX exhibited the lowest interfacial tension and the strongest emulsification ability. AX promoted protein adsorption on the oil phase surface, and the desorption energy of the composite particles at the oil/water interface increased accordingly. The stability of an emulsion stabilized by AX–WPI was confirmed by rheological and microstructural investigations. This study therefore provides theoretical support for the application of such emulsions.

Stress-relieved hollow porous carbon nanoring structures anchored with ZnCo2O4 nanoparticles towards super stable lithium storage

Stress-induced structural mechanical instability is a common occurrence in the electrode material during electrochemical cycling, especially for composite material systems. The structural mechanics engineering of nanocomposites comprising electrochemical active materials and carbon with novel structures holds great promise in addressing this issue. However, conventional carbonaceous materials often encounter challenges in long-term durability and high specific capacity stemming from their intrinsic uneven stress distribution and few active sites. Herein, finite element analysis reveals that the ring-like structure effectively mitigates stress concentration from expansion and possesses high packing density, outperforming traditional nanosphere and nanocube architectures. Accordingly, nanocomposites consisting of hollow porous nanostructured N-doped carbon nanorings (N-CNRs) anchored with bimetallic ZnCo2O4 nanoparticles are designed, which exhibit an extraordinary cycling performance for lithium storage with 96.4 % capacity retention following 1000 cycles and an impressively low storage degradation rate of 0.00357 % per cycle, as well as displaying an excellent specific capacity (1218 mA h/g at 0.1 A g−1) and outstanding rate performance (565 mA h/g at 5.0 A g−1). The well-engineered design nanocomposite features the synergistic effect of electrochemically active ZnCo2O4 nanoparticles integrated with structurally stable carbon nanorings for enhanced electrochemical performance.

Mechanical behaviour and instability mechanism of sandstones with impact tendency under different loading paths

ABSTRACT To reveal the instability and failure mechanism of pillars with impact tendency, the Brazilian test, uniaxial compressive test, cyclic loading and unloading (CLU) tests were performed on sandstones which had impact tendency. The stress drop phenomenon was obvious in the fracture stage during the Brazilian test. The main tensile crack with penetration type appeared. Under the CLU condition, the CLU had a significant effect in enhancing the mechanical character of rocks. Under the combined loading, the character stress of rocks tested with the CLU was greater than the uniaxial loading. Moreover, the greater the first cyclic threshold, the greater the character stress of rocks. Under the uniaxial loading, the failed samples showed tensile fractures. The damage location of the samples was closely related to the Poisson effect and the ending face effect. With the electron microscope which had the same magnification, the crack deterioration degree of samples under the uniaxial loading was greater than the CLU condition. Moreover, with the first cycle threshold increasing, the surface roughness of rocks gradually decreased. The quantity of secondary micro cracks gradually decreased. The propagation and penetration phenomenon gradually disappeared. The micro structure and loading properties of rocks were affected by the bonding force and structural characters between the internal structure and matrix. Based on the micro-seismic signal of the damaging threshold, the seismic source damage location can be located. Moreover, the pillar-typed burst area can be forewarned. This research benefits predicting the pillar-typed burst disaster.

Synthesis and performance study of amphoteric polymer suspension stabilizer for cementing slurry at ultra-high temperature

As the number of ultra-deep wells increases, maintaining the suspension stability of cement slurry at ultra-high temperatures becomes increasingly challenging; the development of a suspension stabilizer suitable for ultra-high temperature environments is imperative. Therefore, this study synthesized a temperature-resistant polymer suspension stabilizer (LHAP) using 2-acrylamide-2-methylpropanesulfonic acid (AMPS), N, N-dimethyl acrylamide (DMAA), 4-acryloylmorpholine (ACMO), and quaternary ammonium cationic hydrophobic long-chain monomer hexadecyl dimethylallyl ammonium chloride (DMAAC-16) as raw materials. It was applied to maintain the suspension stability of cement slurry at ultra-high temperatures. The molecular structure and molecular weight of LHAP were characterized and tested using infrared spectroscopy, nuclear magnetic hydrogen spectroscopy, and Ubbelohde viscometer. The thermal stability and viscosity-temperature performance of LHAP were measured using thermogravimetric analysis and rheometer, respectively. Through the segmented density difference testing of cement stone columns, the suspension stability effect of LHAP on cement slurry under high temperature was evaluated. The suspension stabilization mechanism of LHAP was studied through fluorescence probe testing, variable temperature UV visible light testing, variable temperature particle size distribution testing, Zeta potential analysis, Environmental Scanning Electron Microscopy (ESEM) analysis, and scanning electron microscopy (SEM) analysis. The results indicated that the polymer suspension agent LHAP had excellent temperature resistance, and the molecules didn’t undergo significant thermal degradation below 302 ℃. At high temperatures of 220 ℃, LHAP could maintain the suspension stability of cement slurry, and the segmented density difference of cement columns was less than 0.01 g/cm3. Mechanism analysis revealed that in addition to enhancing temperature resistance by introducing sulfonic acid groups and rigid rings, LHAP also effectively maintains the stability of the slurry suspension at ultra-high temperatures by coordinating electrostatic interactions and molecular associations. LHAP can effectively solve the settlement instability problem of cement slurry under ultra-high temperature, which is beneficial for improving the safety and quality of cementing construction in ultra-deep wells.

Atomic-Scale Scanning of Domain Network in the Ferroelectric HfO2 Thin Film.

Ferroelectric HfO2-based thin films have attracted much interest in the utilization of ferroelectricity at the nanoscale for next-generation electronic devices. However, the structural origin and stabilization mechanism of the ferroelectric phase are not understood because the film is typically nanocrystalline with active yet stochastic ferroelectric domains. Here, electron microscopy is used to map the in-plane domain network structures of epitaxially grown ferroelectric Y:HfO2 films in atomic resolution. The ferroelectricity is confirmed in free-standing Y:HfO2 films, allowing for investigating the structural origin for their ferroelectricity by 4D-STEM, high-resolution STEM, and iDPC-STEM. At the grain boundaries of <111>-oriented Pca21 orthorhombic grains, a high-symmetry mixed-(R3m, Pnm21) phase is induced, exhibiting enhanced polarization due to in-plane compressive strain. Nanoscale Pca21 orthorhombic grains and their grain boundaries with mixed-(R3m, Pnm21) phases of higher symmetry cooperatively determine the ferroelectricity of the Y:HfO2 film. It is also found that such ferroelectric domain networks emerge when the film thickness is beyond a finite value. Furthermore, in-plane mapping of oxygen positions overlaid on ferroelectric domains discloses that polarization is suppressed at vertical domain walls, while it is active when domains are aligned horizontally with subangstrom domain walls. In addition, randomly distributed 180° charged domain walls are confined by spacer layers.

Role of secondary hydrogen injection on flame stabilization of ammonia/air swirling flames

Ammonia is widely recognized as one of the most advanced hydrogen carriers and can be utilized as a fuel in gas turbines. Premixing hydrogen into the ammonia carbon free fuel system can substantially enhance stable limits, but it significantly promotes cross-reactions, leading to increased NO production. Recent findings related to other fuels suggest that the alternative approach for mitigating combustion instabilities involves introducing minimal pure hydrogen at the chamber inlet in a non-premixed mode. This may introduce a novel approach to stabilize ammonia/air swirl flames by extending the stability through a minimal hydrogen via secondary injection, with minimal impact on increasing nitrogen oxide emissions. In the present study, the flame stabilization mechanism and nitrogen oxide emission behaviors of swirl ammonia/air flames by a secondary hydrogen injection were compared with the premixed ammonia/ hydrogen/air flames. OH-/NO-PLIF and PIV techniques were applied to reveal the lean blow-off characteristics and the reacting flow features. The NOx emissions were measured by the FTIR gas analyzer. The large eddy simulation method with a developed dynamic thickened flame model was employed to further reveal the experimental findings. Experimental results show that the flame stabilization limits are largely depended on the way in which hydrogen is introduced. The secondary hydrogen injection exhibits the stronger enhancement ability for the lean/rich blow-off limits, primarily due to the local diffusion hydrogen flame at the flame root providing more active radicals and higher temperature gases. The NO emission shows an increase with the addition of premixed hydrogen, while in the secondary hydrogen injection, NO emission deteriorates due to higher temperatures, with the NO emission increasing by less than 10% compared with the ammonia flame. In the large eddy simulation analyses, the physical effects of the secondary hydrogen injection enhance the flame stability by increasing the resistance of the flame root to extinction. The heat release rate and the mass fractions of NH and H near the flame root are significantly increased by 2% secondary hydrogen injection. The enhancement of the ammonia decomposition process is stronger with secondary hydrogen injection than with fully premixed hydrogen addition. For 2% secondary hydrogen injection case, the local hydrogen injection to form a non-premixed combustion mode can provide much higher capability to increase the local heat release rate compared to the fully premixed mode.Novelty and significance statement: Introducing small amount of hydrogen to ammonia flame can effectively improving the flame stabilization in a swirl combustor. In this study, it is found that the flame stabilization limits are largely depended on the way in which hydrogen is introduced. Comparing the way of premixing hydrogen in the unburned mixture, a larger effect on blow-off limits extension was found when introducing a separate non-premixed hydrogen at the chamber inlet, which is mentioned as the secondary hydrogen injection. The lean blow-off limits can be extended from about 0.67 to 0.59 when only introducing 2% secondary hydrogen injection by heat value. The NO emission shows in the secondary hydrogen injection, NO emission deteriorates by less than 10% compared with the ammonia flame. A thickened flame model for non-premixed combustion was established and verified adequate with velocity field and flame structure. The mechanisms of enhancing flame stabilization by hydrogen introduction including physical and chemical effects for premixing and injection cases were revealed. Furthermore, the difference in the mechanisms of the two cases was emphasized.

Wide pH, Adaptable High Internal Phase Pickering Emulsion Stabilized by a Crude Polysaccharide from Thesium chinense Turcz.

The ultrasound-assisted extraction conditions of Thesium chinense Turcz. crude polysaccharide (TTP) were optimized, and a TTP sample with a yield of 11.9% was obtained. TTP demonstrated the ability to stabilize high-internal-phase oil-in-water emulsions with an oil phase volume reaching up to 80%. Additionally, the emulsions stabilized by TTP were examined across different pH levels, ionic strengths, and temperatures. The results indicated that the emulsions stabilized by TTP exhibited stability over a wide pH range of 1-11. The emulsion remained stable under ionic strengths of 0-500 mM and temperatures of 4-55 °C. The microstructure of the emulsions was observed using confocal laser scanning microscopy, and the stabilization mechanism of the emulsion was hypothesized. Soluble polysaccharides formed a network structure in the continuous phase, and the insoluble polysaccharides dispersed in the continuous phase, acting as a bridge structure, which worked together to prevent oil droplet aggregation. This research was significant for developing a new food-grade emulsifier with a wide pH range of applicability.

Chirality and odd mechanics in active columnar phases.

Chiral active materials display odd dynamical effects in both their elastic and viscous responses. We show that the most symmetric mesophase with 2D odd elasticity in three dimensions is chiral, polar, and columnar, with 2D translational order in the plane perpendicular to the columns and no elastic restoring force for their relative sliding. We derive its hydrodynamic equations from those of a chiral active variant of model H. The most striking prediction of the odd dynamics is two distinct types of column oscillation whose frequencies do not vanish at zero wavenumber. In addition, activity leads to a buckling instability coming from the generic force-dipole active stress analogous to the mechanical Helfrich-Hurault instability in passive materials, while the chiral torque-dipole active stress fundamentally modifies the instability by the selection of helical column undulations.

Structure and mechanisms of stabilization of cytokines EMAP II and AIMP1/p43 in complexes with ligands for biomedical use

Structure and mechanisms of stabilization of cytokines EMAP II and AIMP1/p43 in complexes with ligands for biomedical use

A novel Pickering emulsion gels stabilized by cellulose nanofiber/dihydromyricetin composite particles: Microstructure, rheological behavior and oxidative stability

Particle concentrations (w) and oil content (Φ) are crucial factors influencing the gel stability of Pickering emulsions. To understand the stabilization mechanism comprehensively, we prepared emulsion gels stabilized by CNF/DMY composite particles at various w (0.5–1.5 wt%) and Φ (0.2–0.6, v/v). The microstructure revealed the adsorption of these particles at the oil-water interface, with excess particles forming a three-dimensional network structure in the continuous phase. Rheological studies showed that the network structure of Pickering emulsions was significantly influenced by w and Φ, resulting in improved emulsion gel strength that hindered the movement of oil droplets and oxygen in the continuous phase, thereby enhancing emulsion stability. Three scenarios for the critical strain (γco) were observed: at Φ = 0.2, γco decreased with increasing w, while at Φ = 0.4, γco increased with increasing w. At Φ = 0.6, γco remained relatively constant regardless of w. In conclusion, adjusting particle concentration and oil content enabled the control of microstructure, rheological properties, and antioxidant capacity of emulsion gels. These findings could be a valuable resource for formulating and ensuring the quality of emulsion gel-based products in the food industry.