Polyelectrolyte Hydrogels Research Articles

A diode-like integrated hydrogel for piezoionic generators and sensors

Wearable sensing electronic devices based on hydrogel are gradually developing towards multifunction and portability, however, efficiently harvesting energy from the surrounding environment to power traditional hydrogel-based wearable electronic devices is a major challenge. The assembly of multilayer heterogeneous hydrogels is a potential strategy to address this challenge. Herein, inspired by the structure of diodes, a diode-like integrated hydrogel composed of a three-tier structure of anionic polyelectrolyte hydrogel, polyacrylamide hydrogel and cationic polyelectrolyte hydrogel is developed. By the connection of polyacrylamide hydrogel, the composite hydrogel exhibits excellent structural stability and mechanical properties. Notably, due to the introduction of MXene ion-conducting microchannels, the directional transport of free cations and anions ionized by anionic and cationic polyelectrolytes is achieved, thereby improving the conductivity (74.58 mS/cm), sensing (gauge factor = 7.47) and piezoionic output performance of the composite hydrogel. The composite hydrogel-based sensor can sense tiny facial movements and recognize the direction of human movement, and the composite hydrogel-based piezoionic generator exhibit more efficient mechanical-electric conversion performance, which can output the maximum voltage of 1410mV, current of 28 μA, and power density of 2.9mW/m2 for a composite hydrogel of 5×5 cm2. The integration of multilayer heterogeneous hydrogels proposes a versatile strategy for the development of high-performance hydrogel-based self-powered sensing electronic devices, expanding the application of hydrogels in artificial intelligence and human-computer interaction.

Mechanics of electroadhesion of polyelectrolyte hydrogel heterojunctions enabled by ionic double layers

Mechanics of electroadhesion of polyelectrolyte hydrogel heterojunctions enabled by ionic double layers

Anti‐Swelling 3D Nanohydrogel for Efficient Osmotic Energy Conversion

AbstractOsmotic energy conversion based on reverse electrodialysis (RED) technology has attracted intense attention. As the key component, the ion‐selective membranes should meet the basic requirements of high power density, high mechanical strength, and easy preparation. Polyelectrolyte hydrogel materials are good candidates, due to their high charge density. However, the severe swelling effect decreases the ion selectivity and mechanical strength. To solve this problem, an anti‐swelling 3D nanohydrogel is demonstrated, which is in situ polymerized in the nanoporous polyimide (PI) membrane, exhibiting ultrahigh power density in osmotic energy conversion. Because of the nano‐confinement of the PI matrix, the swelling ratio of the nanohydrogel decreases to 37.5% from 593.2% of the bulk hydrogel. Meanwhile, the hybrid membrane exhibits excellent mechanical strength (≈89.5 MPa). Under a 500‐fold concentration gradient, the nanohydrogel generates a power density of up to 48.5 W m−2, one order of magnitude higher than that of the bulk hydrogel. The anti‐swelling 3D nanohydrogel introduces a new concept in designing separation membranes for osmotic energy conversion.

Simultaneous processing of both handheld biomixing and biowriting of kombucha cultured pre-crosslinked nanocellulose bioink for regeneration of irregular and multi-layered tissue defects

The nanocellulosic pellicle derived from the symbiotic culture of bacteria and yeast (Kombucha SCOBY) is an important biomaterial for 3D bioprinting in tissue engineering. However, this nanocellulosic hydrogel has a highly entangled gel network. This needs to be partially modified to improve its processability and extrusion ability for its applications in the 3D bioprinting area. To control its mechanical and biological properties for direct 3D bioprinting applications, uniform reinforcement of nanocellulose-interacting polymers and nanoparticles in such a prefabricated gel network is essential. In this study, the hydrogel network is partially hydrolyzed with organic acid and subsequently transformed into a 3D bioprintable polyelectrolyte complex with chitosan and kaolin nanoparticles without any chemical crosslinker using a handheld 3D bioprinter. This handheld bioprinter ensures homogeneity in both biomixing and bioprinting of chitosan and kaolin within the modified nanocellulose network for multi-layered bioprinted scaffolds through an extensional shear mechanism. The biomixing simulation, mechanical (static, dynamic, and cyclic), 3D bioprinting, and cellular studies confirm the homogeneous biomixing of kaolin nanoparticles and live cells in this nanocellulose-chitosan polyelectrolyte hydrogel. The combination of SCOBY-derived nanocellulose-chitosan bioink with kaolin nanoparticles and a screw-driven handheld extrusion bioprinter demonstrates a promising platform for layer-by-layer regeneration of complex tissues with homogeneous cell/particle distribution with high cell viability.

Innovating Lubrication with Polyelectrolyte Hydrogels: Sustained Performance Through Lipid Dynamics

AbstractThe lubrication process of natural joint cartilage involves a series of coordinated mechanisms, a key aspect of which is its ability to continuously extract lubricating components from synovial fluid to achieve sustained lubrication. Inspired by this natural phenomenon, this study reports a novel polyelectrolyte hydrogel, specifically integrating ε‐poly‐L‐lysine (ε‐PL), adeptly captures lipids from environment to achieve effective lubrication similar to human joints. The ε‐PL within the hydrogel facilitates the dynamic sequestration of lipids, fostering interfacial self‐assembly. This setup, enriched with highly hydrated lipid head groups, enhances boundary lubrication capabilities for extended performance. Through rigorous evaluation of friction coefficients and supramolecular interactions between the hydrogel and lipids, it identified hydrogen bonding, charge‐dipole, and hydrophobic interactions as key to this self‐assembly. The findings affirm the versatility of polyelectrolytes in synthesizing lubricating hydrogels, bridging the gap to the creation of biomimetic hydrogels that mimic natural lubrication with enhanced durability and efficiency.

Thermal responsive sodium alginate/polyacrylamide/poly (N-isopropylacrylamide) ionic hydrogel composite via seeding calcium carbonate microparticles for the engineering of ultrasensitive wearable sensors

The design of polyelectrolyte hydrogel with unique tensile and adhesive properties which can be applied across disciplines has gradually become a popular trend. However, the phenomenon of global warming and the emergence of extreme weather, it still faces some urgent problems that should be solved, such as the optimal utilization of polyelectrolyte hydrogel across a wide range of temperatures. Herein, a wide temperature sensitivity and conductivity hydrogel based on sodium alginate, acrylamide and N-isopropylacrylamide was constructed, which exhibited excellent adhesion and temperature conductivity. It is worth noting that after the inclusion of CaCO3 and NaCl in the hydrogel, the hydrogel showed excellent tensile properties (fracture strain >2000 %). Within a wide temperature range (−15–50 °C), it exhibits exceptional electrical conductivity (2.75 S ∗ m−1) and sensitivity (GF = 8.76 under high strain). This innovative intelligent polyelectrolyte hydrogel provides suitable strategy for flexible sensors, smart wearable devices and medical monitoring equipment.

Evolving Synergy Between Synthetic and Biotic Elements in Conjugated Polyelectrolyte/Bacteria Composite Improves Charge Transport and Mechanical Properties.

gLiving materials can achieve unprecedented function by combining synthetic materials with the wide range of cellular functions. Of interest are situations where the critical properties of individual abiotic and biotic elements improve via their combination. For example, integrating electroactive bacteria into conjugated polyelectrolyte (CPE) hydrogels increases biocurrent production. One observes more efficient electrical charge transport within the CPE matrix in the presence of Shewanella oneidensis MR-1 and more current per cell is extracted, compared to traditional biofilms. Here, the origin of these synergistic effects are examined. Transcriptomics reveals that genes in S. oneidensis MR-1 related to bacteriophages and energy metabolism are upregulated in the composite material. Fluorescent staining and rheological measurements before and after enzymatic treatment identified the importance of extracellular biomaterials in increasing matrix cohesion. The synergy between CPE and S. oneidensis MR-1 thus arises from initially unanticipated changes in matrix composition and bacteria adaption within the synthetic environment.

A wearable iontophoresis enables dual-responsive transdermal delivery for atopic dermatitis treatment

Atopic dermatitis is a chronic, inflammation skin disease that remains a major public health challenge. The current drug-loading hydrogel dressings offer numerous benefits with enhanced loading capacity and a moist-rich environment. However, their development is still limited by the accessibility of a suitable driven source outside the clinical environment for precise control over transdermal delivery kinetics. Here, we prepare a sulfonated poly(3,4-ethylenedioxythiophene) (PEDOT) polyelectrolyte hydrogel drug reservoir that responds to different stimuli-both endogenous cue (body temperature) and exogenous cue (electrical stimulation), for wearable on-demand transdermal delivery with enhanced efficacy. Functioned as both the drug reservoir and cathode in a Zn battery-powered iontophoresis patch, this dual-responsive hydrogel achieves high drug release efficiency (68.4 %) at 37 °C. Evaluation in hairless mouse skin demonstrates the efficacy of this technology by facilitating transdermal transport of 12.2 μg cm−2 dexamethasone phosphate when discharged with a 103 Ω external resistor for 3 h. The Zn battery-driven iontophoresis results in an effective treatment of atopic dermatitis, displaying reductions in epidermal thickness, mast cell infiltration inhibition, and a decrease in IgE levels. This work provides a new treatment modality for chronic epidermal diseases that require precise drug delivery in a non-invasive way.

Polyelectrolyte gelatin-chitosan hydrogel optimized for 3D bioprinting in skin tissue engineering

Bioprinting is a promising automated platform that enables the simultaneous deposition of multiple types of cells and biomaterials to fabricate complex three-dimensional (3D) tissue constructs. Collagen-based biomaterial used in most of the previous works on skin bioprinting has poor printability and long crosslinking time. This posed an immense challenge to create 3D constructs with pre-determined shape and configuration at high throughput. Recently, the use of chitosan for wound healing applications has attracted huge attention due to its attractive traits such as its antimicrobial properties and ability to trigger hemostasis. In this paper, we optimized polyelectrolyte gelatin-chitosan hydrogel for 3D bioprinting. Modification to the chitosan was carried out via the oppositely charged functional groups from chitosan and gelatin at a specific pH of ~pH 6.5 to form polyelectrolyte complexes. The polyelectrolyte hydrogels were evaluated in terms of physical interactions within polymer blend, rheological properties (viscosities, storage and loss modulus), printing resolution at varying pressures and feed rates and biocompatibility. The polyelectrolyte gelatin-chitosan hydrogels formulated in this work was optimized for 3D bioprinting at room temperature to achieve high shape fidelity of the printed 3D constructs and good biocompatibility with fibroblast skin cells.

Chitosan‒gellan gum polyelectrolyte hydrogel beads containing tea tree oil microcapsules: Preparation, characterization and application

Encapsulation can be applied for essential oil protection, increasing the probability of its application in food preservation. In this study, tea tree oil (TTO) microcapsule powder (MP) was prepared by a spray‒drying approach with soy protein isolate (SPI) and fructooligosaccharide (FOS) as wall materials and were subsequently further encapsulated by chitosan (CH) and gellan gum (GG) via a polyelectrolyte complex coacervation approach. The hydrogel beads prepared with a GG mass ratio of 25% presented the best appearance and the densest internal structure. FTIR and Raman spectral analyses demonstrated the generation of hydrogen bonds between CH and GG. Thermogravimetric analysis confirmed that complex coacervates formed by CH and GG as wall materials can improve the thermal stability of TTO. Owing to the excellent barrier properties of the hydrogel beads, the hydrogel beads maintained high DPPH and ABTS free radical scavenging activities after storage. Moreover, the sustained release of TTO hydrogel beads has potential for preserving fresh-cut banana. These discoveries indicate that hydrogel beads can be used as ideal carriers of essential oils such as TTO and may be used in food preservation in the future.

An Overview on the Adhesion Mechanisms of Typical Aquatic Organisms and the Applications of Biomimetic Adhesives in Aquatic Environments.

Water molecules pose a significant obstacle to conventional adhesive materials. Nevertheless, some marine organisms can secrete bioadhesives with remarkable adhesion properties. For instance, mussels resist sea waves using byssal threads, sandcastle worms secrete sandcastle glue to construct shelters, and barnacles adhere to various surfaces using their barnacle cement. This work initially elucidates the process of underwater adhesion and the microstructure of bioadhesives in these three exemplary marine organisms. The formation of bioadhesive microstructures is intimately related to the aquatic environment. Subsequently, the adhesion mechanisms employed by mussel byssal threads, sandcastle glue, and barnacle cement are demonstrated at the molecular level. The comprehension of adhesion mechanisms has promoted various biomimetic adhesive systems: DOPA-based biomimetic adhesives inspired by the chemical composition of mussel byssal proteins; polyelectrolyte hydrogels enlightened by sandcastle glue and phase transitions; and novel biomimetic adhesives derived from the multiple interactions and nanofiber-like structures within barnacle cement. Underwater biomimetic adhesion continues to encounter multifaceted challenges despite notable advancements. Hence, this work examines the current challenges confronting underwater biomimetic adhesion in the last part, which provides novel perspectives and directions for future research.

Extended rubber-elasticity model for non-Gaussian isotropic hyperelasticity of polyelectrolyte hydrogels undergoing curl-to-stretch transition

The nature of extremely high stretchability in hydrogels with a non-Gaussian elasticity has been extensively investigated. However, there are few studies on curl-to-stretch transitions of condensed polymer networks in polyelectrolyte hydrogels and their non-Gaussian hyperelasticity. In this study, an extended rubber-elasticity model was developed to investigate different mechanical behaviors, e.g., S-shaped and J-shaped stress-elongation ratio curves, where the condensed polymer networks in polyelectrolyte hydrogels undergo a curl-to-stretch transition and present a non-Gaussian isotropic hyperelasticity. A free-energy equation was formulated to describe the curl-to-stretch transitions and their thermomechanical conformations of condensed polymer networks, based on the free energy functions of elasticity, electrostatics and hydrophobicity. A constitutive relationship between stress and elongation ratio was then proposed to describe the non-Gaussian isotropic hyperelasticity in polyelectrolyte hydrogels, and effects of segment number, charged segment fraction and salt concentration on the mechanical behaviors were studied. Moreover, a segmental length criterion of condensed polymer networks was proposed to distinguish the S-shaped and J-shaped stress-elongation ratio curves. Finally, experimental data reported in literature were applied to verify the effectiveness of the proposed theoretical models. This study aims to provide a new thermomechanical criterion for non-Gaussian isotropic hyperelasticity in polyelectrolyte hydrogels undergoing the curl-to-stretch transition.

Anionic Hofmeister Effect Regulated Conductivity in Polyelectrolyte Hydrogels for High-Performance Supercapacitor.

The Hofmeister effect not only affects the stability and solubility of protein colloids but also has specific effects on the polymer molecules. Here, the impact of the Hofmeister effect on the electrochemical properties of polyelectrolyte hydrogels at room temperature and subzero temperature studied for the first time. Polyelectrolyte hydrogels exhibit an anti-polyelectrolyte effect in low concentrations of ammonium salt, while they exhibit an obvious Hofmeister effect in high concentrations of ammonium salt. Kosmotropic ions demonstrate strong interaction with water molecules or polymer chains, resulting in the reduction of conductivity of polyelectrolyte hydrogels. However, chaotropic ions exhibit weak interactions with water molecules or molecular chains, leading to an increase in conductivity. The Hofmeister effect has a more significant effect on the polyzwitterion electrolyte. The conductivity of polyzwitterion hydrogel soaked in chaotropic ion is up to 6.2 mS cm-1 at -40°C. The supercapacitor assembled by polyzwitterion electrolytes maintains a capacitance retention rate of 85% and ≈100% coulomb efficiency after 15 000 cycles at -40°C. This study elucidates the influence of the Hofmeister effect on conductivity in polyelectrolytes and expands the regulatory approach for improving the performance of energy storage devices.

Spongy polyelectrolyte hydrogel with Janus porous for solar-driven interfacial evaporation and sustainable seawater desalination

Janus-structured hydrogels exhibit excellent advantages in interfacial solar desalination due to their hydrophilicity and low evaporative enthalpy of evaporation, as well as the better salt resistance and mechanical properties. In this research, a simple one-step self-stratification foaming technique is employed to transform hydrogels into Janus structured for seawater desalination. Polyvinyl alcohol (PVA), poly (diallyldimethylammonium chloride) (PDADMAC), and a photothermal material (carbon black, CB) are mechanically stirred with a foaming agent (sodium dodecyl sulfate, SDS), allowing for full mixing and air incorporation, ultimately forming a sponge-like polymeric electrolyte hydrogel with abundant Janus pore structures (PANS-J). The formation of Janus pores in the hydrogel is attributed to the flocculation and high density of hydrophilic PDADMAC, causing it to sink during gelation while hydrophobic PVA floats to the surface. The Janus structure produced by this method reduces heat loss and enhances evaporation performance, achieving a pure water evaporation rate of 3.35 kg m−2 h−1 under sunlight (1 kW m−2). Moreover, quaternary ammonium ions on PDADMAC effectively separate anions and cations in saltwater, reducing salt ion diffusion into the evaporator, preventing premature pore structure blockage, and thus improving long-term evaporator performance which can improve the salt resistance and mechanical properties. By combining these advantages, Janus evaporators hold significant promise for solar-driven water purification and other applications.

Minimal actuation and control of a soft hydrogel swimmer from flutter instability

Micro-organisms propel themselves in viscous environments by the periodic, nonreciprocal beating of slender appendages known as flagella. Active materials have been widely exploited to mimic this form of locomotion. However, the realization of such coordinated beating in biomimetic flagella requires complex actuation modulated in space and time. We prove through experiments on polyelectrolyte hydrogel samples that directed undulatory locomotion of a soft robotic swimmer can be achieved by untethered actuation from a uniform and static electric field. A minimal mathematical model is sufficient to reproduce, and thus explain, the observed behavior. The periodic beating of the swimming hydrogel robot emerges from flutter instability thanks to the interplay between its active and passive reconfigurations in the viscous environment. Interestingly, the flutter-driven soft robot exhibits a form of electrotaxis whereby its swimming trajectory can be controlled by simply reorienting the electric field. Our findings trace the route for the embodiment of mechanical intelligence in soft robotic systems by the exploitation of flutter instability to achieve complex functional responses to simple stimuli. While the experimental study is conducted on millimeter-scale hydrogel swimmers, the design principle we introduce requires simple geometry and is hence amenable for miniaturization via micro-fabrication techniques. We believe it may also be transferred to a wider class of soft active materials.

Natural Polyelectrolyte Hydrogels with Two Types of Cross-Links with Different Energy

For the first time, gels of a polymer cross-linked by two types of ionic cross-links of different energies, namely trivalent chromium (III) ions and divalent iron (II) ions, were prepared. The negatively charged polysaccharide xanthan, a polyelectrolyte of natural origin, was used as a polymer. A study of xanthan gels cross-linked with each cross-linker separately was carried out to identify the optimal concentrations of each cross-linker for the production of a double cross-linked gel. The mechanical properties of hydrogels under oscillatory shear deformations were then studied. It was demonstrated that the simultaneous use of two cross-linkers resulted in a synergistic increase in the elastic modulus (plateau storage modulus) compared to gels cross-linked with each cross-linker separately. For a gel with two types of cross-links, the elastic modulus was 16 Pa. In contrast, for gels cross-linked with either chromium (III) cations or iron (II) cations, the elastic modulus was approximately 0.6 and 0.5 Pa, respectively. The strong effect can be attributed to the different nature of cross-linking between xanthan macromolecules and chromium (III) and iron (II) cations, as well as the different strength of the cross-links formed. The optimal range of pH values was determined in which a synergistic increase in the elastic modulus of gels with two types of cross-links was observed compared to the corresponding gels cross-linked with each cross-linker separately. Consequently, the concurrent utilisation of two cross-linking agents that generate cross-links with disparate energy levels represents an efficacious strategy to improve the tensile strength of polymer hydrogels.

Xanthan gum and chitosan polyelectrolyte hydrogels with self-reinforcement of Zn+2 for wound dressing applications

A straightforward methodology was employed for the self-reinforcement of zinc ions (Zn+2) within the polyelectrolyte complexation of xanthan gum (XG) and chitosan (CS) using D (+)-glucuronic acid-δ-lactone (GDL) as an acidifying agent in aqueous environment. The self-reinforcement and polyelectrolyte complexation between XG and CS was primarily achieved by maintaining acidic conditions through the use of GDL. GDL produces H+ ions, not only in converting ZnO to Zn+2 ions but also in facilitating the polyelectrolyte complexation between XG and CS. The confirmation of Zn+2 self-reinforcement was evident through the disappearance of ZnO, as observed in Fourier transform infrared spectroscopy and X-ray diffraction patterns. The compressive properties of self-reinforced Zn+2 within XG-CS hydrogels were evaluated, and their compressive strength was found to depend significantly on the reinforcement of ZnO nanoparticles. Incorporating 1 wt% ZnO improved the compressive strength of the hydrogels, decreasing further with an increasing amount of ZnO (3 wt%), as confirmed by compressive analysis. Detailed SEM images conclusively demonstrated The hydrogels porous structure, and elemental analysis verified the presence of Zn+2 ions. The antibacterial activity of Zn+2 reinforced XG-CS hydrogel showed excellent antibacterial activity towards both positive and negative bacteria. Furthermore, the biocompatibility analysis was assessed through an in vitro study that confirmed good biocompatibility towards NIH3T3 fibroblast cells. Thus, a robust inhibitory effect of bacterial growth and biocompatibility of developed hydrogels hold promise in advanced wound dressings for infected wounds.

Antibacterial Silver Nanoparticle Containing Polydopamine Hydrogels That Enhance Re-Epithelization.

A polydopamine polyelectrolyte hydrogel was developed by ionic crosslinking dextran sulfate with a copolymer of polyethyleneimine and polydopamine. Gelation was promoted by the slow hydrolysis of glucono-δ-lactone. Within this hydrogel, silver nanoparticles were generated in situ, ranging from 25 nm to 200 nm in size. The antibacterial activity of the hydrogel was proportional to the quantity of silver nanoparticles produced, increasing as the nanoparticle count rose. The hydrogels demonstrated broad-spectrum antibacterial efficacy at concentrations up to 108 cells/mL for P. aeruginosa, K. pneumoniae, E. coli and S. aureus, the four most prevalent bacterial pathogens in chronic septic wounds. In ex vivo studies on human skin, biocompatibility was enhanced by the presence of polydopamine. Dextran sulfate is a known irritant, but formulations with polydopamine showed improved cell viability and reduced levels of the inflammatory biomarkers IL-8 and IL-1α. Silver nanoparticles can inhibit cell migration, but an ex vivo human skin study showed significant re-epithelialization in wounds treated with hydrogels containing silver nanoparticles.

Non-swelling polyelectrolyte complex hydrogels with tissue-matchable mechanical properties for versatile wet wound closure

The stable adhesion of hydrogel-based bioadhesives with tissue-matchable mechanical properties in biological environments remains a significant challenge. In this work, we propose a polyethyleneimine-polyacrylic acid (PEI-PAA, PEA) double-network polyelectrolyte hydrogel with swelling resistant capacity and tunable mechanical properties via one-step UV-initiated polymerization. Driven by electrostatic interactions and polymer-chain entanglement, this PEA hydrogel displays a distinctive microphase separation behavior, which facilitates a wide tunability in mechanical properties. Specifically, the modulus varies from 0.4 MPa to 106 MPa, and the toughness ranges from 1479 kJ/m3 to 7641 kJ/m3, respectively. Besides, the microphase separation endows PEA hydrogel with notable anti-swelling properties in saline, TBS buffer, and blood, leading to consistent adhesion to diverse moist tissues. We further demonstrate that our PEA hydrogels provide matchable mechanical properties and long-lasting adhesion to rat skin and arteries, which promote skin injury healing and effectively halt artery rupture bleeding in vivo. This work presents a straightforward method to generate non-swelling hydrogels and offers novel insight into the development of bioadhesives to meet diverse mechanical requirements.

Recoverable and degradable carboxymethyl chitosan polyelectrolyte hydrogel film for ultra stable encapsulation of curcumin

Hydrogels have shown great potential for application in food science due to their diverse functionalities. However, most hydrogels inevitably contain toxic chemical cross-linking agent residues, posing serious food safety concerns. In this paper, a curcumin/sodium alginate/carboxymethyl chitosan hydrogels (CSCH) were prepared by self-assembly of two oppositely charged polysaccharides, carboxymethyl chitosan and sodium alginate, to form a three-dimensional network encapsulating curcumin for extending food shelf life. The network structure of the CSCH film confirmed by FTIR, XRD, and XPS was mainly formed by electrostatic interactions. The chemical stability of CSCH network encapsulated curcumin was 4.2 times greater than that of free curcumin, with excellent gas barrier, antimicrobial, antioxidant, and biosafety properties. It was found that CSCH films reduced dehydration, prevented nutrient loss, inhibited microbial growth, and lowered the respiration rate, which effectively maintained the quality of mango and prolonged its shelf-life up to 11 days. Notably, CSCH films possessed the properties of rapid recycling (10 mins) and biodegradability (53 days). This polysaccharide-based hydrogel film provides a viable strategy for the development of green and sustainable food packaging.