Diabetic refractory wounds are a prevalent and severe complication of diabetes, whose pathological progression is jointly mediated by multiple factors, including oxidative stress imbalance, chronic inflammation, impaired angiogenesis, bacterial infection, and biofilm formation. Current clinical hydrogel dressings generally suffer from drawbacks such as single-function performance, potential toxicity of nano-components, static networks incompatible with dynamic wound conditions, and the absence of bionic repair signals. Therefore, they cannot simultaneously satisfy the dual repair requirements of complex pathological microenvironments and dynamic mechanical properties for diabetic wounds. In this study, a multi-functional dynamically responsive composite hydrogel (MC group) with high-efficiency antioxidant, antibacterial, and pro-angiogenic capacities was fabricated. Using SDS-C18 micelles as hydrophobic units, a rigid–flexible dual-network framework was constructed with polyvinyl alcohol (PVA) and methacrylated hyaluronic acid (HAMA). Manganese dioxide nanozymes were introduced to scavenge reactive oxygen species (ROS) and mitigate oxidative stress. Calcium-ion-mediated dynamic micelle reconstruction was adopted to regulate the hydrophilic–hydrophobic balance, while achieving antibacterial effects and facilitating tissue regeneration. In vitro experiments verified that the MC hydrogel possesses mechanical properties well-matched to human soft tissues (fracture stress: 25 kPa) and excellent biocompatibility (cell viability > 100%, hemolysis rate: only 0.13%). It also exhibits prominent antioxidant activity (DPPH radical-scavenging rate: 36.95%), antibacterial performance (>99.86% bactericidal rate against Staphylococcus aureus, survival rate of Escherichia coli reduced to 15.95%), and cell-migration-promoting activity (endothelial cell migration rate of 83.72% and mouse fibroblast migration rate of 90.88% within 24 h). In the full-thickness skin defect model of diabetic mice, the wound-healing rate reached 99% on day 16. Moreover, it promoted ordered collagen deposition, skin appendage regeneration, and functional microvascular reconstruction, thereby accomplishing high-quality tissue repair. This design synergistically intervenes in multiple pathological links of diabetic wounds, overcomes several key limitations of existing dressings, and provides an innovative strategy for developing smart dressings.
The service life of SBS-modified asphalt mixtures with physical gel structures is strongly influenced by the loading sequence–interaction coupling effects. However, conventional linear models fail to accurately capture the influence of such coupling effects on fatigue life. This study, therefore, aims to develop a life prediction method for SBS-modified asphalt mixtures that explicitly accounts for the loading sequence–interaction coupling effects. First, indirect tensile monotonic loading tests, as well as constant-amplitude and variable-amplitude indirect tensile repeated loading tests were conducted to determine the fatigue life of SBS-modified asphalt mixtures under different loading modes. Subsequently, a viscoelastic fatigue damage model was developed to analyze the accumulation of fatigue damage in SBS-modified asphalt mixtures. Subsequently, the effects of loading sequence and loading interaction on the fatigue damage accumulation process in SBS-modified asphalt mixtures were investigated. Based on these analyses, a nonlinear fatigue damage accumulation model considering the loading sequence–interaction coupling effects was established. Finally, a nonlinear fatigue damage accumulation factor was introduced for developing a fatigue life prediction model for SBS-modified asphalt mixtures considering the loading sequence–interaction coupling effects. The results indicate that the low–high (σlow–σhigh) and high–low (σhigh–σlow) loading sequences, respectively, retard and accelerate the fatigue damage accumulation process of SBS-modified asphalt mixtures. Consequently, the corresponding cumulative fatigue life fractions are greater than 1 and less than 1, respectively. Furthermore, the resulting fatigue life is positively correlated with the first-level fatigue life fraction under the σlow–σhigh sequence but negatively correlated under the σhigh–σlow sequence. The developed nonlinear fatigue damage accumulation model can accurately track the nonlinear fatigue damage accumulation of SBS-modified asphalt mixtures. The established nonlinear fatigue life prediction model accurately predicts the fatigue life of SBS-modified asphalt mixtures with physical gel structures under cyclic loading with variable stress amplitudes.
Polymer aerogels have attracted increasing attention as lightweight porous materials for thermal insulation, separation, adsorption, remediation, and other environmental applications. Their low density and tunable surface chemistry also make them suitable for converting renewable, recycled, and waste-derived feedstocks into value-added materials. However, their overall sustainability remains difficult to assess because most studies focus on material properties, whereas solvent use, drying energy, processing yield, durability, regeneration, and end-of-life pathways are reported less consistently. This review examines sustainable polymer aerogels from the perspectives of cleaner production and waste valorization and focuses on two main features. First, a unified multiscale framework of structure, formation, and performance links network formation mechanisms, pore architecture, and macroscopic behavior across biomass-derived, thermoset, dynamic covalent, hybrid, and recycled polymer aerogels, which are compared in terms of feedstock origin, processing intensity, functional performance, durability, and circularity. Second, structure–property mapping is combined with sustainability-constrained, AI-guided design, with environmental descriptors treated as optimization objectives from the outset rather than as post hoc justifications. Particular attention is given to waste and secondary resources, including agricultural residues, textile waste, paper waste, recycled poly(ethylene terephthalate), and end-of-life tire fibers. The review also discusses how life-cycle assessment, service-based functional units, and minimum reporting standards can help assess whether sustainability claims are supported by measurable environmental benefits. Several recurring limitations emerge from the literature: sustainability is often discussed only qualitatively, processing data are insufficient to support robust life-cycle assessments, solvent exchange and drying remain major environmental hotspots, and circularity claims frequently conflate bio-based content, biodegradability, recyclability, and reusability. Finally, the review discusses how data-driven tools, including literature mining, machine learning, and multi-objective optimization, can support polymer-aerogel design when environmental descriptors are included from the beginning of materials development. The review also proposes a reporting and design roadmap for future work toward polymer aerogels that combine useful performance with lower resource intensity and credible end-of-life value retention.
Polymeric micelles represent a fundamental self-assembled architecture of gel-based soft materials and have emerged as promising nanocarriers for anticancer drug delivery. Their performance is largely governed by the block composition of constituent copolymers, and understanding their self-assembly behavior provides critical insights into the rational design of gel-related drug delivery systems. In this work, dissipative particle dynamics (DPD) simulations were performed to systematically investigate two types of mixed drug-loaded micellar systems self-assembled from a triblock copolymer mPEG-b-poly(2-(diethylamino)ethyl methacrylate)-b-PMMA (PDEAEMA, hereafter referred to as the DMA block for brevity) with either a diblock copolymer PDEAEMA-b-PMMA (polymer B) or PPEGMA-b-PDEAEMA (polymer C). By tailoring the ratios of hydrophobic (MMA, the constituent block of PMMA) and pH-sensitive (DMA) blocks, the protonation-responsive behavior, structural stability, drug loading capacity, and release kinetics of the micelles were comprehensively examined. The simulation results demonstrate that: (1) increasing the hydrophobic block ratio accelerates the protonation-triggered micellar swelling and drug release because the increased hydrophobic content enhances the core compactness which, upon protonation, generates a stronger driving force for chain extension, yet an optimal ratio (+16 MMA units) exists beyond which excessive hydrophobic blocks suppress release due to core densification; (2) increasing the pH-sensitive block ratio significantly enhances the maximum drug loading capacity (from 9.83% to 12.22% for the A/C system), but exerts only limited influence on the release rate; (3) the A/C mixed micelles with higher PEG content exhibit superior structural stability and drug loading capacity, while the A/B system with higher MMA content displays more sensitive pH-responsiveness. These findings reveal a competing mechanism between “protonation-driven force” and “structural resistance,” providing mesoscopic theoretical guidance for the rational design of pH-responsive polymeric nanocarriers and self-assembled soft materials via block ratio modulation.
Silk fibroin (SF)- and silk sericin (SS)-based antibacterial hydrogels are increasingly engineered as local antimicrobial platforms, yet cross-study interpretation is limited by inconsistent material reporting and by conflation of bacterial inhibition with tissue repair. We performed a structured evidence-mapping and critical synthesis of a frozen 2020–July 2026 corpus of 94 references. The original 46-record core map was re-audited at the original-article level: 43 full-text-verified, non-retracted primary studies were retained for detailed evidence grading, 2 records available only at abstract/database level were retained descriptively but not graded, and 1 subsequently retracted study was excluded from quantitative synthesis. Among the 43 graded studies, metal-ion/nanozyme/catalytic systems were most common (12/43, 27.9%), followed by release-mediated (11/43, 25.6%), multimodal (9/43, 20.9%), contact-active/anti-adhesive (6/43, 14.0%), and light-responsive systems (5/43, 11.6%). Sixteen studies (37.2%) used deliberately infected animal models, whereas only 4 (9.3%) reached a biofilm or adherent-bacteria-level endpoint in the graded map. Biological claim ceilings (C0–C5) are assessed independently from translation gates spanning material identity, reproducibility, mechanism, host safety, sterilization/storage, resistance, long-term fate, and deployment. Across mechanisms, SF and SS most often function as structural, interfacial, or transport-regulating matrices; direct silk-dependent bactericidal causality remains uncommon. The central translational deficit is failure to quantitatively link silk molecular identity and network architecture to antimicrobial exposure, bacterial killing, host selectivity, and long-term material fate.
Vaginal drug delivery offers a critical route for local treatments but is limited by short formulation residence times. This study describes a thermosensitive in situ gel prepared by the cold-dissolution method from a ternary blend of Pluronic F127, Carbopol 940, and HPMC for localized vaginal therapy. We used ibuprofen as a model drug selected for its reported anti-inflammatory and antiproliferative activity. The hydrogels exhibited a constant gelation temperature of 28 °C and high viscosity under simulated physiological conditions; ibuprofen incorporation further reduced susceptibility to gravitational leakage. FTIR, XRD, and DSC analyses confirmed stable physical cross-linking of the polymer network and amorphous molecular dispersion of ibuprofen. Peppas–Sahlin modelling revealed a controlled, sustained release profile (>50% over 24 h) predominantly governed by Fickian diffusion (69%). The blank hydrogel exhibited high biocompatibility (>75% viability). In contrast, the ibuprofen-loaded matrix exhibited a concentration-dependent cytotoxic effect on HeLa cervical cancer cells, reducing cell viability to ~12% at the full extract concentration. Overall, this ternary hydrogel platform represents a stable, promising vehicle for sustained local administration of ibuprofen in the vaginal microenvironment.
The sequential phases of tissue healing—inflammation, proliferation, and remodeling—demand distinct pharmacokinetic profiles that conventional drug delivery systems fail to provide, creating a “chronotherapy gap” that contributes to chronic wound pathologies. Hydrogels, with their highly tunable network structures, offer a unique platform to program release kinetics in synchrony with these healing timelines. This review systematically examines design strategies for phase-synchronized hydrogel systems, categorized into three hierarchical paradigms: intrinsic network control (crosslinking density, degradation kinetics, and architectural engineering) that pre-programs release profiles; extrinsic/responsive control (endogenous pH/ROS/MMP/glucose and exogenous NIR/ultrasound/electro/magnetic triggers) that enables on-demand phase-shifting; and integrated systems that combine passive spatial compartmentalization with active responsiveness. We survey representative applications across cutaneous wounds, bone defects, cartilage, tendon, myocardial, and neural tissues, highlighting both common design principles and tissue-specific adaptations. Key translational bottlenecks—including in vivo–in vitro discrepancies, cargo stability, sterilization challenges, and regulatory complexity—are critically examined, alongside emerging frontiers such as closed-loop biosensing, artificial intelligence-driven design, and four-dimensional printing. We conclude that the field is evolving from passive drug depots toward active therapeutic synchronizers, where material programming is set to the body’s biological clock, offering a transformative paradigm for regenerative medicine.
Intrauterine adhesion (IUA) is a fibrotic disorder resulting from aberrant repair following injury to the endometrial basal layer, leading to menstrual abnormalities, infertility, recurrent miscarriage, and pregnancy complications. Although hysteroscopic adhesiolysis remains the primary clinical treatment, the rate of postoperative re–adhesion is still high, especially in patients with moderate–to–severe IUA. Moreover, mechanical separation alone is often insufficient to restore intact endometrial architecture and reproductive function. Hydrogels, with their hydrated three–dimensional networks, extracellular matrix (ECM)–mimicking properties, injectability, biodegradability, tissue adhesion, and tunable delivery capacity, have evolved from passive barrier materials into multifunctional therapeutic platforms capable of regulating the pathological microenvironment and promoting tissue regeneration. Recent advances in responsive, self–healing, adhesive, antioxidant, and bioactive cargo–loaded hydrogels have expanded their applications from preventing adhesion formation toward functional endometrial reconstruction. In this review, we summarize recent progress in hydrogel–based IUA therapy, focusing on material composition, structural design, functional modification, therapeutic mechanisms, and translational considerations. Particular emphasis is placed on disease–informed hydrogel engineering strategies that integrate the unique anatomical characteristics of the uterine cavity, injury–associated microenvironment, and dynamic stages of endometrial repair. This perspective provides insights into the development of next–generation hydrogel systems for preventing re–adhesion and restoring reproductive function.
Bacterial infection, biofilm formation, and the associated oxidative stress and persistent inflammation represent major obstacles to wound healing, tissue engineering, and implantable medical devices. Owing to their highly hydrated three-dimensional networks, favorable tissue compatibility, and versatile capacity for functional loading, hydrogels have been widely investigated for the treatment of infected wounds. This review systematically summarizes the major antibacterial mechanisms of hydrogels, including cationic contact-killing, chemical antibacterial activity mediated by metal ions and reactive halogen species, nanozyme-catalyzed reactions and bidirectional regulation of reactive oxygen species, as well as photothermal synergistic antibacterial therapy. Key design strategies are also discussed, including natural polymer-based matrices, multiple dynamic crosslinking, stimuli-responsive controlled release, three-dimensional printing, and spatial compartmentalization. In addition, recent advances in infection-microenvironment regulation, wet-interface adaptation, temporally coordinated tissue repair, and integrated diagnosis and therapy are highlighted. The field is currently shifting from single-mode bacterial eradication toward multistage tissue repair and intelligent theranostics. However, major challenges remain, including balancing antibacterial efficacy with biosafety, achieving reproducible manufacturing and sterilization-compatible formulations, maintaining functional stability during storage, and improving the clinical relevance and standardization of preclinical evaluation. In addition, most smart systems still lack quantitative coupling among pathological signals, therapeutic dosage, and treatment outcomes. Future studies should therefore integrate mechanistic design with manufacturing reproducibility, clinically relevant validation, and quantitative feedback regulation, thereby advancing antibacterial hydrogels from multifunctional proof-of-concept systems toward precise, controllable, and clinically translatable therapeutic platforms.
The global atmospheric CO2 concentration continues to rise, leading to increasingly severe greenhouse effects, ocean acidification, and extreme climate events. Therefore, the development of efficient CO2 capture materials is urgently needed. Aerogels, a class of three-dimensional nanoporous solid materials formed by the crosslinking of nanoparticles or polymer molecular chains via the sol–gel process, exhibit outstanding advantages in CO2 capture due to their high specific surface area, tunable nanopores, and abundant surface functionalizable sites. This paper systematically summarizes the preparation methods, including supercritical drying, ambient pressure drying, and freeze drying, reviews the classification and design strategies of aerogel materials, and analyzes the application status of aerogels in scenarios ranging from direct air capture, post-combustion flue gas capture, and natural gas purification to carbon sequestration. Finally, future development trends are prospected, aiming to provide a reference for the design and large-scale application of high-performance aerogel-based CO2 adsorbents.
As cutting-edge semiconductor devices become smaller and more densely packed (i.e., ultra large-scale integration, ULSI), there is an increased risk of parasitic capacitance preventing proper device operation. There is consequently growing interest in the development of low-permittivity dielectric materials to serve as intermetal/interlayer coatings that would minimize this effect. Highly porous aerogels exhibit extremely low dielectric permittivity; silica-based aerogel films, in particular, are candidates for this application. The present report focuses on the synthesis, structure and dielectric permittivity of hydrophobic, tetramethyl orthosilicate (TMOS)-based silica aerogels prepared in disc-form. Using our 3D printed polymer sample holder with few metallic components, we are now able to determine the dielectric permittivity of highly porous, hydrophobic silica aerogels in the very low frequency (VLF) range, 10–27 kHz. Commercial systems that operate in the VLF range include circuits for biological signal processing, characterized by low amplitude and frequency, and circuits that operate in marine environments, where the useful frequency range is limited by acoustic signal deterioration. During impedance measurements, aerogel samples were confined in pure, dry oxygen atmosphere. Low mass density (10–250 mg/cm3) TMOS-based aerogel discs present structural characteristics and relative dielectric permittivity values in the VLF range that are not readily comparable with analogous data reported to date in the relevant literature.
Styrene–butadiene–styrene (SBS)-modified asphalt is a physical polymer gel system in which SBS forms a three-dimensional elastic network within the asphalt matrix. This network structure governs the rheological and mechanical properties of the material, yet the quantitative relationships among processing parameters, material composition, microstructure, and macroscopic performance remain insufficiently understood. This study proposes a multi-scale machine learning framework to establish processing–composition–structure–performance mappings for SBS-modified asphalt gels. A dataset of 1072 experimental samples was compiled from a gene database and supplementary laboratory tests. Ten input features were used to predict four performance indicators: penetration, softening point, ductility, and viscosity at 135 degrees Celsius. Four machine learning models were developed and compared. The support vector machine with radial basis function kernel achieved the highest accuracy for penetration with an R2 value of 0.9997 and for ductility with an R2 value of 0.9996. The artificial neural network performed best for softening point with an R2 of 0.9996, and extreme gradient boosting for viscosity with an R2 of 0.9993. Optuna-based optimization improved the average R2 by 2.1% over default configurations. SHAP analysis identified shear temperature, SBS dosage, and SBS particle size as the most influential factors. The framework enables accurate and interpretable prediction of gel properties and provides a data-driven foundation for material design.
Efficient cutaneous wound healing relies on the phenotypic transition of macrophages toward an anti-inflammatory, pro-reparative M2-like state. Non-healing chronic wounds are pathologically characterized by the breakdown of this polarization balance. In this review, we synthesize recent research on biomaterials fabricated from naturally occurring polysaccharides with intrinsic immunomodulatory activity, mainly represented by hydrogels that modulate macrophage phenotypic transitions. We first dissect the immune microenvironment of wound healing and elaborate on the core regulatory networks governing M1/M2 polarization, with a particular focus on signaling pathways and metabolic reprogramming. On this basis, we classify pro-M2 natural polysaccharides into mannose-containing and mannose-free categories according to their core structural motifs that mediate immunomodulatory activity, and detail their molecular mechanisms, including pattern recognition receptor engagement (MR, Dectin-1, CD44, etc.) and downstream signaling cascades (STAT6, PI3K/Akt, NF-κB, etc.). Representative polysaccharides such as konjac glucomannan (KGM), Ganoderma lucidum polysaccharide (GLP), chitosan (CS) and hyaluronic acid (HA) are discussed with a clarified structure–activity relationship (SAR). Finally, we highlight emerging design strategies for multi-functional immunomodulatory hydrogels, including mechano-biochemical coupling platforms and spatiotemporally controlled delivery systems, and analyze ongoing controversies and translational bottlenecks in this field. The relationship between material structure and function enables the rational design of purpose-built polysaccharide dressings that regulate immunity. This review highlights these materials as promising preclinical platforms for chronic wound management, although their clinical translation requires further validation.
This study evaluated the impact of varying quercetin (Q; 0.01–0.05%) incorporations on the quality, functional, structural, and bio-functional properties of CHOS-enriched (0.75%; w/w) pangasius surimi gel. Gel samples were analyzed for gel strength, texture profile, colour, water-holding capacity (WHC), protein interactions, structural changes, thermal stability, antioxidant/antimicrobial activities, and sensory parameters. Results indicated that Q significantly decreased pH while exerting a minor effect on proximate composition. Incorporation of Q up to 0.04% (Q4) remarkably improved breaking force (654.70 g), deformation (1.13 cm), gel strength (707.82 g cm), hardness, and WHC (90.66%), while reducing expressible moisture content and proteolysis. Molecular interactions, FT-IR spectra, SDS-PAGE, and SEM confirmed that Q promoted cross-linking of myosin heavy chains via hydrogen bonding and hydrophobic interactions, creating a denser, more compact gel matrix with higher thermal stability. Additionally, Q addition significantly enhanced 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)/2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) in a concentration-dependent manner, though lightness and whiteness indices decreased due to Q’s natural yellow pigment.
Owing to their small size, micron-scale accuracy, rapid response, and biocompatibility, microrobots are emerging as a promising tool for biomedical applications, especially in targeted drug delivery and minimally invasive microsurgery. The architectural configuration of microrobots governs their locomotion performance, environmental adaptability, and functional integration capacity. Although existing reviews have systematically organized this field by actuation strategies, material categories, or application scenarios, a comprehensive summary centered on the structural evolution paradigm remains conspicuously absent. This review aims to fill this gap by systematically tracing the evolutionary trajectory of microrobot structures from rigid architectures through soft configurations to rigid–soft integrated systems. First, the foundational principles underlying structural evolution were introduced, encompassing the connotation of structure, fluid dynamics constraints, and the drivers of structural innovation. Then, rigid microrobot architectures were systematically elucidated, including geometric asymmetric and surface asymmetric designs. Subsequently, soft microrobot structures, covering both predefined deformation structures and dynamically reconfigurable architectures, were discussed. Finally, the rigid–soft integrated systems reconciling compliance and performance through spatial heterogeneity or temporal stiffness modulation were systematically surveyed. This evolutionary trend reflects a transition from optimizing individual performance parameters toward achieving balanced functional synergy across distinct task phases. Based on the current research progress, this review also presents future research directions in data-driven structural optimization, reconfigurable architectures, and autonomous structural intelligence, offering strategic guidance for next-generation microrobot design.
To elucidate the influence of mineral composition on CO2 mineralization and mechanical reinforcement, three synthetic tailing systems representing felsic, high-calcium silicate, and magnesium-carbonate compositions were prepared using a full-component reconstitution approach. Their carbonation kinetics, phase evolution, pore structure, and mechanical response were systematically investigated. The alkaline buffering duration increased in the order of felsic < high-calcium silicate < magnesium-carbonate types, with plateau durations of approximately 300, 650, and 2000 s, respectively. TG-DTG, XRD, and FTIR analyses collectively indicated composition-dependent formation of carbonate-bearing products, with the magnesium-carbonate type showing the strongest carbonate-related signals. SEM observations further revealed precipitation on particle surfaces and within interparticle regions, suggesting precipitation-induced particle bonding. Nitrogen adsorption–desorption measurements showed pronounced pore-structure reorganization after mineralization; the average pore size converged to approximately 7.5–7.9 nm, whereas the specific surface area decreased in all systems. The failure loads of the felsic and high-calcium silicate types increased by factors of 2.97 and 3.81, respectively. The mineralized magnesium-carbonate type exhibited the highest apparent compressive strength (53.69 kPa). These results demonstrate clear composition-dependent relationships among carbonation, pore evolution, and mechanical response in the synthetic systems. Because the materials were prepared from analytical-grade reagents and no complete carbon balance was established, the results should be regarded as mechanistic model-system evidence rather than quantitative estimates of CO2 sequestration in natural tailings.
Resorcinol–formaldehyde (RF)-derived porous carbons have attracted considerable attention as anode materials for lithium-ion batteries because of their tunable pore structures and continuous carbon frameworks. However, conventional one-factor-at-a-time experiments do not readily allow the relative effects of multiple preparation factors to be systematically compared within a unified experimental framework. In this study, a mixed-level Design of Experiments (DOE) was employed to systematically investigate the effects of solid content, gelation temperature, R/C ratio, combined gelation and acid-washing/aging times, and drying method on the BET specific surface area, total pore volume, and dominant pore size of RF-derived porous carbons. Representative preparation conditions were subsequently selected to prepare PC-1 and PC-2. Both samples exhibited predominantly amorphous mesoporous carbon structures and similar electrochemical response profiles. PC-1 exhibited a higher reversible specific capacity and slightly more favorable electrochemical kinetics. These concurrent observations suggest an association between the pore-structure characteristics and electrochemical behavior of the selected samples. PC-1 delivered an initial charge capacity of 416.67 mAh g−1 with an initial Coulombic efficiency of 79.31%. After 200 cycles at 0.1 A g−1, it retained a reversible capacity of 307.86 mAh g−1, corresponding to a capacity retention of 88.64% relative to the second-cycle charge capacity. These results indicate that, within the investigated design space, the DOE approach provides an exploratory basis for jointly comparing the statistical evidence and practical effect magnitudes of the preparation factors and for selecting representative candidates with favorable pore-structure characteristics. The integration of DOE-based factor screening with subsequent structural and electrochemical validation provides an experimentally grounded framework for relating preparation parameters to pore-structure responses and lithium-storage behavior, thereby supporting the rational development of RF-derived porous carbon anodes for lithium-ion batteries.
Perilla (Perilla frutescens (L.) Britt.) seed protein, an underutilized resource derived from medicinal and edible plants, was subjected to ultrasound (400 W, 20 min), pH-shifting (pH 12.0, 1 h), and high-pressure homogenization (90 MPa, 3 cycles), applied individually or in combination, and subsequently fermented with probiotics to induce gel formation. The triple combination (pH-shifting + high-pressure homogenization + ultrasound) produced the highest solubility increase (129%), smallest particle size, greatest random coil content, and maximal surface hydrophobicity and free sulfhydryl level. The triple-modified protein gels exhibited a highly homogeneous microstructure. Meanwhile, these gels achieved significant improvements (p < 0.05) in multiple functional and rheological properties, including gel strength, water-holding capacity, viscosity, and storage modulus, as well as the viable count. These results demonstrate that combined application of three physical modifications effectively restructures perilla seed protein and markedly improves its gelation behavior under fermentation, supporting its potential as a novel ingredient for fermented plant-protein gels or yogurt-like products.
Diabetic chronic wounds face multiple intractable healing obstacles including sustained inflammation, severe infection, insufficient angiogenesis and defective collagen deposition. Current dressings fail to simultaneously relieve all these pathological defects. Herein, we constructed a carrier-free binary self-assembled Glycyrrhizic acid monoammonium salt–Berberine (GB) hydrogel composed of berberine and glycyrrhizic acid monoammonium salt, which forms interconnected nanofiber networks via one-pot thermally assisted small-molecule co-assembly without chemical crosslinking or exogenous polymer carriers. Relying on intermolecular non-covalent interactions, this single supramolecular material integrates anti-inflammatory, broad-spectrum antibacterial, pro-angiogenic, and collagen-regenerative multifunctions, which simultaneously ameliorates multiple core pathological obstacles of diabetic wounds within one formulation. We systematically characterized its physicochemical features, biocompatibility, and antibacterial and anti-inflammatory activities, as well as in vivo wound repair performance. This hydrogel formed uniform nanofibrous architectures with favorable viscoelastic properties and pH-dependent sustained release. In vitro assays verified its outstanding biosafety, broad-spectrum bacteriostasis against Escherichia coli and Staphylococcus aureus, and potent inhibitory effects on pro-inflammatory cytokines TNF-α and IL-6, with bacterial inhibition rates reaching ~88% against E. coli and ~70% against S. aureus. In diabetic mouse full-thickness infected wound models, the GB hydrogel simultaneously alleviated local inflammation, accelerated wound closure and facilitated ordered collagen deposition and mature microvessel formation, achieving a 73.10% wound closure rate at day 7 and 58.01% collagen deposition fraction at day 14, thus exhibiting equivalent or superior repair capacity compared with commercial hydrogel dressings. This carrier-free supramolecular system based on natural herbal small molecules provides a safe, convenient, and integrated therapeutic strategy for diabetic infected chronic wounds, with promising clinical translation potential.
Gelatin hydrogels combine biological origin, biodegradability, abundant chemical functionality, and broad processability, but their native thermoreversible physical networks generally lack the stability required for sustained operation. Crosslinking overcomes this limitation while regulating hydration, mechanics, transport, degradation, and responsiveness. This review examines gelatin hydrogel crosslinking from a structure–property–function perspective, connecting molecular design with physicochemical characterization and functional performance. Temperature-induced gelation and ion-mediated physical interactions are compared with small-molecule- and coupling-agent-mediated, enzyme-catalyzed, and photoinduced covalent crosslinking strategies, highlighting their different balances among reversibility, stability, processability, and biocompatibility. Particular attention is given to the characterization methods required to relate junction chemistry and network organization to swelling, thermal behavior, mechanical response, degradation, and molecular or ionic transport. These relationships are evaluated across drug delivery and controlled release, tissue engineering and wound healing, food packaging, preservation and delivery, water remediation and environmental management, wearable sensing and bioelectronics, and energy storage. Across these fields, the central challenge is not to maximize crosslinking, but to balance network stability with the molecular mobility required for function. By integrating complementary crosslinking mechanisms with multiscale characterization, gelatin can be engineered as a programmable platform for advanced soft materials.
