Search Results (200)

The global demand for food has been increasing, presenting new challenges in meeting this demand. To address this growing need, the use of coating technology through nanoemulsions shows great potential. The use of thyme essential oil stabilized by chitosan nanoparticles offers a promising and sustainable approach for the development of edible coatings. Chitosan was extracted from shrimp shell waste and used to produce nanoparticles via the ionotropic gelation method, using sodium tripolyphosphate (TPP) as a crosslinking agent. To prepare the nanoemulsions, thyme essential oil was used as the dispersed phase, combined with an aqueous phase containing chitosan nanoparticles and Tween 80 as the emulsifier. Two techniques were employed to produce nanoemulsions: high-pressure homogenization and ultrasonication. Nanoemulsion formulations with different concentrations were prepared and characterized in terms of droplet size (Z-Average) and stability using dynamic light scattering (DLS). The average droplet sizes obtained were above 100 nanometers for samples produced via high-pressure homogenization and below 100 nanometers for those prepared using ultrasonication. Analysis of variance (ANOVA) confirmed that both the method (p = 0.002) and the oil phase concentration (p < 0.001) had statistically significant effects on droplet size. Regression analysis showed that oil concentrations below 2.0 g (w/w) increased droplet size, while concentrations above 4.0 g (w/w) significantly reduced it (p < 0.05). However, physical stability tests conducted at 5 °C for 30 days showed consistent values across both formulations, with only minor fluctuations, suggesting overall good stability. Full article

Low-molecular-weight gelators (LMWGs) have attracted growing attention as versatile alternatives to conventional polymeric thickeners and gelators, owing to their ability to form three-dimensional fibrillar networks through non-covalent self-assembly and to undergo reversible sol–gel transitions in response to external stimuli. Among the various stimuli that can be exploited, pH represents a particularly attractive trigger given its direct relevance to biological and physiological environments. This review focuses on three categories of pH-responsive LMWGs that have shown notable progress over the past decade yet remain relatively underexplored in the literature. First, N-oxide-type hydrogelators are discussed, with emphasis on amide amine oxide-based surfactants and pyridine-N-oxide frameworks. The pH-dependent protonation of the N-oxide moiety modulates intermolecular hydrogen bonding, thereby governing self-assembly and gel formation. The structural versatility of these gelators enables rational tuning of aggregate morphology and confers clear pH and temperature responsiveness. Second, recent advances in phenylboronic acid-based LMWGs are highlighted. Although boronic acid derivatives have long been studied as dynamic crosslinking units in polymeric hydrogels, 3-isobutoxyphenylboronic acid was recently identified as the first example of phenylboronic acid functioning as an LMWG, in which gelation is driven primarily by hydrogen bonding and pH responsiveness is exploited for stimuli-triggered gel disruption rather than gel formation. Third, pH-responsive orthogonal self-assembly systems are reviewed. Representative examples include multicomponent hybrid hydrogels combining pH-activated LMWGs with polymer gelators for controlled drug release, pH-triggered self-sorting of two LMWGs without any polymeric component, and bio-based orthogonal hydrogels composed of a glucolipid LMWG and cellulose nanocrystals. For each system, both advantages and remaining limitations are critically assessed. Collectively, this review aims to provide a timely overview of emerging trends in pH-responsive LMWG research and to offer perspectives on the rational design of next-generation stimuli-responsive soft materials. Full article

This study presents a risk assessment of asphaltene–resin–paraffin deposition (ARPD) in the producing formations of the XIII reservoir unit of the Uzen oil field at a late stage of development. The crude oil is characterized by an extremely high paraffin (wax) content of up to 29 wt.%. Long-term operation of the reservoir pressure maintenance (RPM) system with cold water injection has resulted in significant reservoir cooling, with temperatures declining from the initial 60–65 °C to 20–30 °C in zones of intensive waterflooding. To refine the critical phase transition temperatures of paraffin components, a dynamic laboratory approach was applied using a Wax Flow Loop system, which simulates wax deposition processes under flowing conditions. The results indicate that the wax appearance temperature (WAT) ranges from 41.0 to 44.0 °C, significantly exceeding the current bottomhole temperatures in the cooled zones of the reservoir. Intensive bulk crystallization of paraffins occurs within the temperature interval of 33.5–35.0 °C, while loss of oil flowability is observed at 25–34 °C, corresponding to the gelation and structural network formation of wax crystals under reduced thermal conditions. The obtained results confirm the inevitability of bulk oil structuring and solid wax phase precipitation directly within the reservoir porous medium. This process leads to blockage of low-permeability interlayers, deterioration of filtration properties, and a reduction in the displacement efficiency factor by 20–35%. Under the current thermal regime, ARPD should therefore be considered not merely as an operational flow assurance issue, but as a systemic factor limiting reservoir development efficiency. The research results substantiate the need to transition from reactive ARPD removal methods to proactive management of the thermal regime of the reservoir and wells, as well as to the differentiated application of thermal and chemical treatment methods. Full article

Soy protein concentrate (SPC) undergoes continuous thermal and structural changes during passage through a cooling die, yet these changes are often interpreted using viscosity-based descriptions that do not explicitly account for structural development rate (SDR). This study developed a rheology-guided framework to analyze SPC behavior in a three-stage cooling die by integrating isothermal and non-isothermal rheological characterization with computational fluid dynamics (CFD). SPC samples containing 76, 78, and 80% moisture were evaluated using strain sweep, frequency sweep, viscosity, time sweep, and temperature sweep tests. Lower moisture promoted stronger structure development, higher viscosity, and faster gelation. For the 76% moisture sample, peak SDR increased from 6.66 Pa/s at 50 °C to 22.46 Pa/s at 100 °C, while the time to peak decreased from 937 to 360 s. During non-isothermal cooling, the major structure development occurred in the 80–50 °C interval, where ΔG′ reached 4902.54 Pa at 76% moisture. CFD analysis showed that the gelation-kinetics-based model predicted both pressure and extrudate temperature more accurately than the viscosity-based model. Pressure RMSE ranged from 8.57 to 14.43 kPa for the kinetic model, compared with 11.31 to 22.39 kPa for the viscosity model. These results demonstrate that the three-stage cooling die should be interpreted as a coupled thermal, flow, and structure-development domain. Full article

The development of new advanced functional materials from low-molecular-weight gelators and their new potential applications have occupied a considerable place in research. The present study involves the design of dipeptide-based organogelators with enhanced hydrogen bonding network potentials and phase-selective capacities, possessing a minimum gelation concentration of 0.2–0.4% w/v in different fluids. Seven new dipeptide organogelators were prepared based on a one-step reaction from two-component salt forms, the combination of Nε-alkanoyl-L-lysine ethyl ester with N-alkanoyl-L-amino acids (L-alanine, L-leucine, and L-phenylalanine), with high yields of up to 90. All the gel materials were extremely stable at room temperature, having a shelf life of several months, and formed gels in pharmaceutical fluids such as ethyl palmitate, ethyl myristate, and ethyl laurate, 1,2-propanediol, and liquid paraffin (oils widely used in pharmaceutical formulations), which meet the criteria of biological materials delivery. Their gelation properties were evaluated by rheological measurements. A very significant breakthrough in the current study is that organogels remove the toxic dye, crystal violet (CV), from water in a phase-selective manner with an extremely low gelator concentration. The dye and gelators are successively recovered via ethanol precipitation after the completion of the phase extraction process. Molecular dynamic calculations provide evidence for the 3D structures of the gels. Full article

Sol–gel phase transitions are complex far-from-equilibrium processes characterized by limited reproducibility, whose origin remains poorly understood and rarely quantified. We investigated the thermally induced sol–gel transition of agar using turbidimetry. A phenomenological model was applied to extract key kinetic parameters (maximum absorbance, maximum rate, and characteristic times) from 96 independent replicates. Variability was quantified and compared with that of an enzymatic reaction exhibiting similar sigmoidal kinetics, allowing for separation of experimental, intrinsic, and nonergodic contributions. Agar gelation displays markedly higher variability. The total variability (CV ≈ 16%) exceeds both the experimental error (1–2%) and the nonergodic contribution (≈2%), demonstrating that it predominantly arises from intrinsic process dynamics. Variability increases sharply during early stages of gelation and then evolves more gradually, indicating that stochastic nucleation and network formation pathways drive divergent kinetic trajectories despite identical initial conditions. Variability in gelation is therefore not a measurement artifact but an intrinsic hallmark of the sol–gel transition. This inherent stochasticity limits the predictive power of deterministic models, particularly at meso- and microscopic scales, and should be considered a fundamental feature of gel-forming systems. Our approach provides a quantitative framework for characterizing variability in phase transitions and may be extended to more complex biological and soft matter systems. Full article

Limited mechanical robustness and prompt proteolytic degradation preclude wider biomedical application of supramolecular peptide hydrogels. Low-molecular-weight dehydropeptides represent a promising class of hydrogelators, owing to their enhanced proteolytic stability, high self-assembly propensity, biocompatibility, and tunable rheological and drug-release properties. Herein, we prepared a small library of N-succinylated dehydrotripeptides (Suc-L-Xaa-L-Phe-Z-ΔPhe-OMe/-OH; Xaa = Phe or Val), together with the canonical analogs (Suc-L-Phe-L-Phe-L-Phe-OMe/-OH), to assess whether in addition to proteolytic resistance, dehydropeptides offer clear advantages over canonical peptides in terms of self-assembly, gelation efficacy, mechanical performance, and cargo release. Peptide self-assembly, hydrogel formation, and supramolecular organization were investigated by fluorescence and circular dichroism (CD) spectroscopy, molecular dynamic (MD) simulations, Thioflavin T hydrogel staining, ATR-FTIR spectroscopy, transmission electron microscopy (TEM), and rheological measurements. Drug-release performance was evaluated using methyl orange as a model cargo. Overall, the dehydropeptide-based hydrogels displayed enhanced gelation efficacy, improved mechanical properties, and sustained release profiles compared to canonical analogs. Spectroscopic analysis (CD and ATR-FTIR) and molecular dynamic simulations indicated that the dehydropeptides preferentially self-assemble into more ordered supramolecular fibrils, with extended β-sheet-like packing, whereas the canonical peptides predominantly populate more disordered backbone environments. Proteolysis assays with α-chymotrypsin revealed that both canonical and dehydropeptide methyl esters underwent chymotrypsin-catalyzed ester hydrolysis. Importantly, only the canonical dicarboxylic acid underwent further proteolytic degradation. The dehydropeptide dicarboxylic acids revealed fully resistant to proteolysis over extended time periods. These results demonstrate that the incorporation of dehydroamino acid into peptides enables control over supramolecular packing, nanofibrillar network architecture, rheology, and cargo release. This report raises the profile of relatively underexplored dehydropeptide-based soft materials as promising high-performance biomaterials for technological and biomedical applications. Full article

Neurodegenerative diseases feature diverse pathological protein aggregates, including Lewy bodies in Alzheimer’s disease (AD) and skein-like filaments in amyotrophic lateral sclerosis (ALS). The physical mechanisms underlying this morphological diversity remain unclear. Here, we demonstrate that aggregation of the prion-like domain of hnRNPA1 (A1PrD), implicated in AD and ALS, is driven by solution composition and phase transition dynamics. Utilizing 3D timelapse and fluorescence lifetime imaging microscopy, we show that solution conditions modulate phase separation, gelation, and fibrillation, resulting in distinct structures such as fibril, gel, and starburst morphologies. Homotypic and heterotypic interactions between A1PrD and RNA were observed to shift the balance between pathological and physiological condensates. Importantly, amyloid-rich starbursts displayed prion-like infection capabilities toward amyloid-poor condensates. Our findings highlight how the interplay between solution composition and kinetic balances of liquid-liquid phase separation, gelation, and fibrillation shapes the diverse pathological aggregate morphologies characteristic of neurodegenerative diseases. Full article

Fast-curing polyurethane (PU) systems are attractive for high-throughput manufacturing, but quantifying cure kinetics, gelation, and cure-dependent glass transition temperature ($T_g$) is difficult, especially at a low degree of cure (DoC). Here, a fast-reacting BASF PU formulation was studied using non-isothermal differential scanning calorimetry (DSC) at multiple heating rates, rheometry at 50 °C, and molecular dynamics (MD) simulations to extend $T_g\left(\alpha \right)$in the low-DoC regime. DSC provided reaction enthalpy and conversion histories, and Kamal–Sourour (KS) parameters were identified by robust nonlinear fitting, reproducing conversion and curing rate profiles (R² > 0.99 and >0.95). Rheology indicated gelation between 475 and 625 s (DoC ≈ 0.53), and DSC-based $T_g$ at uncured, gelation, and fully cured states, established the experimental $T_g$ trend. MD (LAMMPS) with topological crosslinking and NPT thermal scans extracted $T_g$from density–temperature slopes at selected DoC points. Experimental and MD $T_g$ data were fused with Gaussian process regression constrained by the DiBenedetto relationship (5-fold cross-validation), giving λ ≈ 0.29 and confidence intervals. This framework links kinetics, gelation, and $T_g$ evolution for fast-curing PU and identifies the low-DoC region as the main source of uncertainty. Full article

Background/Objectives: High-voltage, low-current electric shocks inflict superficial second-degree burns on the skin, accompanied by a vicious cycle of excessive oxidative stress and inflammation. As efficient treatment of such electrical burns remains a clinical challenge, we explored the efficacy of an injectable thermosensitive chitosan hydrogel engineered with an antioxidant agent (astaxanthin) and an anti-inflammatory agent (ibuprofen) for the treatment of high-voltage, low-current electrical burn injuries. Methods: The proposed CS/AST/IBU hydrogel was prepared and its thermosensitivity was characterized. Subsequently, the hydrogel was injected into the wounds of male Sprague–Dawley (SD) rats subjected to electrical burn injury (20 kV, 3 mA). Finally, a series of experiments were performed to elucidate the dynamics of wound healing and the mechanisms by which the hydrogel promotes wound repair. Results: The injectable hydrogel, through its thermally responsive gelation effect at 37 °C, adapts to the complex irregularities of the wound surface. This facilitates the release of astaxanthin and ibuprofen throughout the wound, which collectively diminish the formation of reactive oxygen species and MDA. Furthermore, it enhances the synthesis of endogenous antioxidants such as SOD, CAT, and GSH; encourages collagen deposition; stimulates the development of dermal appendages; and fosters neovascularization. It interrupts the deleterious cycle of oxidative stress and inflammation mediated by the NF-κB signaling pathway, thereby suppressing the expression of pro-inflammatory markers such as TNF-α, CD11b, and IL-1β while upregulating CD163, an anti-inflammatory receptor. Conclusions: The use of this multipronged, contour-adaptive hydrogel represents an effective strategy for complex wound management and demonstrates broad therapeutic potential for superficial second-degree electrical burns caused by high-voltage, low-current discharge. Full article

This study investigates the development and characterization of bioactive films incorporating silver nanoparticles (AgNPs) into biocompatible polymers, namely alginate and chitosan, fabricated using two methods, spin-coating and drop-casting, and aiming to enhance their antimicrobial properties. Dynamic light scattering (DLS) and electrophoretic mobility (EM) of the film precursor solutions revealed significant changes in the nanoparticles’ size and Zeta potential (ZP), reflecting the influence of polymer coatings. Alginate contributed to high electrostatic stability due to its negative charge, while chitosan facilitated specific interactions with negatively charged surfaces. Raman spectroscopy revealed that spin-coating conditions did not successfully result in film formation, highlighting the need for further optimization. Therefore, subsequent characterization studies were conducted only for the films formed by drop-casting. Topographical and nanomechanical assessments of these drop-cast films, using atomic force microscopy (AFM) and force spectroscopy, demonstrated that AgNPs reduced adhesion and elasticity in alginate films, while increasing rigidity and adhesion in chitosan-based films. Antimicrobial tests confirmed the efficacy of AgNPs in both precursor solutions and polymer films, with chitosan-based films that retained structural integrity, which makes them suitable for prolonged applications, while alginate films displayed rapid gelation upon hydration, potentially advantageous in short-term applications. The findings underscore the potential of these biopolymer-AgNP composites in creating antimicrobial materials for food packaging, wound dressings, and other biomedical applications. However, challenges related to film deposition methods, such as spin-coating, require further optimization to improve film formation and reproducibility. Full article

This study addresses the challenge of annular gas migration control during the waiting-on-cement (WOC) period in managed pressure cementing for formations with narrow safe pressure windows. A dynamic pressure compensation optimization strategy is proposed by integrating a composite mechanistic model with experimental validation. Based on the hydration degree (T) model, a predictive model for static gel strength development was established. By coupling the gelation-induced suspension effect with cement slurry volumetric shrinkage, a static hydrostatic pressure decline model was developed. Experimental results indicate that the prediction errors of the proposed models are all within 7%, demonstrating improved accuracy compared with traditional empirical approaches and classical shear stress models. In addition, a testing methodology was developed to characterize pressure transmission efficiency during the WOC process, revealing its dynamic attenuation behavior. Experimental results show that when the static gel strength of anti-gas-migration cement slurry reaches 240 Pa, the pressure transmission efficiency ranges from 45% to 49%. Based on these findings, a wellhead backpressure calculation model incorporating the evolution of pressure transmission efficiency was established, providing a quantitative basis for annular pressure management during cement setting. Full article

CO₂ flooding is an effective technique for enhancing oil recovery in low-permeability reservoirs. However, it is often hindered by severe CO₂ channeling. This challenge is particularly pronounced in near-wellbore regions with large pressure differentials and in fractured reservoirs, where high CO₂ injection rates and rapid breakthrough require channel blocking systems with high mechanical strength and excellent CO₂-resistant performance. In this work, a smart responsive polymer was synthesized and subsequently crosslinked with a highly active phenolic resin crosslinking agent to develop a smart responsive polymer gel channel blocking system. The resulting gel exhibits CO₂-responsive strength enhancement and excellent CO₂-resistant performance. The static and dynamic gelation behaviors, nonlinear rheological properties, CO₂-resistant performance, channel blocking, and enhanced oil recovery performance of the smart responsive polymer gel were systematically investigated. The results demonstrate that the polymer gel maintains good structural stability during dynamic transport in the reservoir and does not undergo significant strength degradation under shear conditions. Moreover, the smart responsive polymer gel exhibits excellent CO₂-resistant performance within a temperature range of 80–110 °C, salinity up to 10 × 10⁴ mg/L, and pressure up to 20 MPa. Moreover, the system shows a significant enhancement in channel blocking and enhanced oil recovery performance, highlighting its promising potential for effective CO₂ flooding channel blocking in low-permeability reservoirs. Full article

This study presents a microfluidic platform for non-Newtonian fluid viscosity sensing, integrating a high-flow-rate flow field stabilizer to mitigate flow uniformity limitations under elevated flow rate conditions. Building upon an established dual-phase laminar flow principle that determines relative viscosity via channel occupancy, this research aimed to extend the measurable viscosity range from 1–10 cP to 1–50 cP, which covers viscosity regimes relevant to biomedical fluids, dairy products during gelation, and low-to-moderate viscosity industrial liquids. A flow stabilizer was developed through computational fluid dynamics simulations, optimizing three key design parameters: blocker position, porosity, and the number of outlet paths. The N5 design proved most effective, providing over 50% reduction in standard deviation for asymmetric velocity distribution in high-flow simulations. The system was validated using simulated blood and dairy samples, achieving over 95% viscosity accuracy with less than 5% sample volume error compared to conventional viscometers. The chip successfully captured viscosity transitions during milk acidification and gelation, demonstrating excellent agreement with standard measurements. This low-volume, high-precision platform offers promising potential for applications in food engineering, biomedical diagnostics, and industrial fluid monitoring, enhancing microfluidic rheometry capabilities. Full article

Extrusion processing can induce gel-like network formation in plant proteins, enabling the advancement of structured meat alternatives with tailored textural properties. In this study, extrusion-induced gelation behavior of isolated mung bean protein (IMBP) was systematically investigated during the manufacture of low-moisture meat analogs (LMMA). The effects of key processing variables, rotational speed of the screw, moisture level, and processing temperature on gel network development, hydration behavior, and textural responses were evaluated using response surface methodology as an analytical framework. Increasing moisture content promoted protein hydration and facilitated the formation of continuous gel-like interactions, resulting in enhanced pore development and water-holding capacity. Variations in screw speed and processing temperature further modulated the extent of protein denaturation and network consolidation, influencing nitrogen solubility and mechanical properties. While the integrity index remained relatively insensitive to processing conditions, structural and functional responses exhibited clear dependencies on extrusion-induced gelation dynamics. The extrusion conditions of 39% moisture, 216 rpm, and 159 °C promoted the development of a well-defined protein network, leading to improved functional properties. These findings provide mechanistic insight into extrusion-driven gelation of IMBP and highlight its potential as a protein matrix for gel-based meat analog applications. Full article