Double Network Hydrogels Research Articles

Soft hydrogel semiconductors with augmented biointeractive functions.

Hydrogels, known for their mechanical and chemical similarity to biological tissues, are widely used in biotechnologies, whereas semiconductors provide advanced electronic and optoelectronic functionalities such as signal amplification, sensing, and photomodulation. Combining semiconducting properties with hydrogel designs can enhance biointeractive functions and intimacy at biointerfaces, but this is challenging owing to the low hydrophilicity of polymer semiconductors. We developed a solvent affinity-induced assembly method that incorporates water-insoluble polymer semiconductors into double-network hydrogels. These semiconductors exhibited tissue-level moduli as soft as 81 kilopascals, stretchability of 150% strain, and charge-carrier mobility up to 1.4 square centimeters per volt per second. When they are interfaced with biological tissues, their tissue-level modulus enables alleviated immune reactions. The hydrogel's high porosity enhances molecular interactions at semiconductor-biofluid interfaces, resulting in photomodulation with higher response and volumetric biosensing with higher sensitivity.

Conductive-Polymer-Based Double-Network Hydrogels for Wearable Supercapacitors.

In the field of contemporary epidermal bioelectronics, there is a demand for energy supplies that are safe, lightweight, flexible and robust. In this work, double-network polymer hydrogels were synthesized by polymerization of 3,4-ethylenedioxythiophene (EDOT) into a poly(vinyl alcohol)/poly(ethylene glycol diacrylate) (PVA/PEGDA) double-network hydrogel matrix. The PEDOT-PVA/PEGDA double-network hydrogel shows both excellent mechanical and electrochemical performance, having a strain up to 498%, electrical conductivity as high as 5 S m-1 and specific capacitance of 84.1 ± 3.6 mF cm⁻2. After assembling two PEDOT-PVA/PEGDA double-network hydrogel electrodes with the free-standing boron cross-linked PVA/KCl hydrogel electrolyte, the formed supercapacitor device exhibits a specific capacitance of 54.5 mF cm⁻2 at 10 mV s-1, with an energy density of 4.7 μWh cm-2. The device exhibits excellent electrochemical stability with 97.6% capacitance retention after 3000 charging-discharging cycles. In addition, the hydrogel also exhibits great sensitivity to strains and excellent antifouling properties. It was also found that the abovementioned hydrogel can achieve stable signals under both small and large deformations as a flexible sensor. The flexible and antifouling PEDOT-PVA/PEGDA double-network hydrogel-based supercapacitor is a promising power storage device with potential applications in wearable electronics.

V2CTx MXene-derived porphyrin-based MOF modified with ZIF-67 as an ultra-stretchable and deformable double-network hydrogel for room temperature detection of dimethylamine

Stretchable and self-adhesive chemical sensors are highly appealing for wearable health and environmental monitoring applications. Here, for the first time, we report V2CTx MXene-derived Porphyrin-based MOF (V-PMOF) modified with Zeolite imidazole framework-67 (ZIF-67) for the room temperature detection of dimethylamine. V-PMOF is synthesized from V2CTx MXene using tetrakis(4-carboxyphenyl)porphyrin (TCPP) as a ligand via a solvothermal route. Thereafter, an optimized wt% ratio (1:1) of ZIF-67 and V-PMOF crosslinked by PVA/polypyrrole (Ppy) is put for lyophilization which yields the V-PMOF@ZIF-67 double-network (DN) hydrogel. Detailed morphological assessment reveals dodecahedron-shaped ZIF-67 particles are evenly distributed on the V-PMOF sheets which are encapsulated in the polymer matrix. This three-dimensional polymeric structure of hydrogel largely enhances the active sites on the surface with abundant oxygen vacancies. The sensor exhibits a dynamic range of 1 ppm to 13 ppm with a low limit of detection (LOD = 3s/σ) of 902 ppb towards dimethylamine detection. Further, quick response/recovery times (3 s/7 s) are observed along with high robustness tosignificant mechanical deformation, including twist (270°), large-range bending, and up to 500% strain without affecting the sensing performance. The remarkable sensitivity is accredited to the abundance of O2 functional groups in polymer chains and the formation of Schottky heterojunction between V-PMOF and ZIF-67, facilitating charge transfer between the heterostructure to dimethylamine during sensing. In addition, the self-adhesive hydrogel-based sensor shows outstanding selectivity against other typical volatile organic compounds (VOCs) such as acetone, ethanol, ammonia, trimethylamine, aniline, and methanol. In overall, this work provides insight into designing extremely flexible sensitive dimethylamine gas sensor as innovative material.

Periosteum-bone inspired hierarchical scaffold with endogenous piezoelectricity for neuro-vascularized bone regeneration

The development of scaffolds for repairing critical-sized bone defects heavily relies on establishing a neuro-vascularized network for proper penetration of nerves and blood vessels. Despite significant advancements in using artificial bone-like scaffolds infused with various agents, challenges remain. Natural bone tissue consists of a porous bone matrix surrounded by a neuro-vascularized periosteum, with unique piezoelectric properties essential for bone growth. Drawing inspiration from this assembly, we developed a periosteum-bone-mimicking bilayer scaffold with piezoelectric properties for regeneration of critical-sized bone defects. The periosteum-like layer of this scaffold features a double network hydrogel composed of chelated alginate, gelatin methacrylate, and sintered whitlockite nanoparticles, emulating the viscoelastic and piezoelectric properties of the natural periosteum. The bone-like layer is composed of a porous structure of chitosan and bioactive hydroxyapatite created through a biomineralization process. Unlike conventional bone-like scaffolds, this bioinspired bilayer scaffold significantly enhances osteogenesis, angiogenesis, and neurogenesis combined with low-intensity pulsed ultrasound-assisted piezoelectric stimulation. Such a scheme enhances neuro-vascularized bone regeneration in vivo. The results suggest that the bilayer scaffold could serve as an effective self-powered electrical stimulator to expedite bone regeneration under dynamic physical stimulation.

Influence of cellulose on the properties of physically cross-linked poly(vinyl alcohol)/Agar double network hydrogels and investigation of multifunctional flexible sensors

With the slogan "double carbon target" coming into the public's view, green, healthy, non-toxic and harmless hydrogel flexible sensors have become one of the research subjects of many staff. But most hydrogels need a crosslinking agent to complete polymerization. In this work, a PVA (poly (vinyl alcohol))/Agar hydrogel material was designed to form three-dimensional reticulated composite hydrogels with a variety of cellulose, and more green and healthy citric acid was used instead of PVA crosslinker to promote hydrogel polymerization. Through the test of four kinds of cellulose, it was found that PVA/HPMC ((Hydroxypropyl)methyl cellulose)/Agar hydrogel has the most outstanding performance, its mechanical property is 1.77 MPa, its elongation at break can reach 766 %, and it has good recovery performance, fatigue resistance and good adhesion. After it is applied to the flexible hydrogel sensor, its gauge factor value is as high as 5.94 under the strain of more than 200 %. When simulating human skin and detecting human motion, the electrical signal changes sensitively and repeatedly, and has a good response when testing temperature and humidity. PVA/HPMC/Agar hydrogel provides a more healthy solution for flexible electronic devices.

Double-Network Hydrogel 3D BioPrinting Biocompatible with Fibroblast Cells for Tissue Engineering Applications.

The present study examines the formulation of a biocompatible hydrogel bioink for 3D bioprinting, integrating poly(ethylene glycol) diacrylate (PEGDA) and sodium alginate (SA) using a double-network approach. These materials were chosen for their synergistic qualities, with PEGDA contributing to mechanical integrity and SA ensuring biocompatibility. Fibroblast cells were included in the bioink and printed with a Reg4Life bioprinter employing micro-extrusion technology. The optimisation of printing parameters included needle size and flow velocities. This led to precise structure development and yielded results with a negligible deviation in printed angles and better control of line widths. The rheological characteristics of the bioink were evaluated, demonstrating appropriate viscosity and shear-thinning behaviour for efficient extrusion. The mechanical characterisation revealed an average compressive modulus of 0.38 MPa, suitable for tissue engineering applications. The printability of the bioink was further confirmed through the evaluations of morphology and diffusion rates, confirming structural integrity. Biocompatibility assessments demonstrated a high cell viability rate of 82.65% following 48 h of incubation, supporting the bioink's suitability for facilitating cell survival. This study introduced a reliable technique for producing tissue-engineered scaffolds that exhibit outstanding mechanical characteristics and cell viability, highlighting the promise of PEGDA-SA hydrogels in bioprinting applications.

Fabrication of Microstructured Hydrogels via Dehydration for On-Demand Applications.

Microstructured hydrogels show promising applications in various engineering fields from micromolds to anisotropic wetting surfaces and microfluidics. Although methods like molding by, e.g., casting as well as 3D printing are developed to fabricate microstructured hydrogels, developing fabrication methods with high controllability and low-cost is an on-going challenge. Here, a method is presented for creating microstructures through the dehydration of double network hydrogels. This method utilizes common acrylate monomers and a mask-assisted photopolymerization process, requiring no complex equipment or laborious chemical synthesis process. The shape and profile of microstructures can be easily controlled by varying the exposure time and the mask used during photopolymerization. By altering the monomer and the mask used for fabricating the second network hydrogel, both convex and concave microstructures can be produced. To showcase the utility of this method, the patterned hydrogel is utilized as a mold to fabricate a polydimethylsiloxane microlens array via soft lithography for imaging application. In addition, a patterned hydrogel surface exhibiting obvious anisotropic wetting properties and open microfluidic devices which can achieve fast directional superspreading within milliseconds are also fabricated to demonstrate the versatility of the method for different engineering fields.

A chemically defined, mechanically tunable, and bioactive hyaluronic acid/alginate double-network hydrogel for liver cancer organoid construction

Liver cancer organoids replicate the pathophysiology of primary tumors, making them ideal for drug screening and efficacy evaluation. However, their growth in complex, variable, animal-derived matrices hinders practical application. Here, we designed an easily accessible, chemically defined, biocompatible double-network hydrogel (HADR) using methacrylated hyaluronic acid (HAMA), sodium alginate (SA), methacrylamide dopamine (DMA), and c(RGDFC) for liver cancer organoid culture. By optimizing critical extracellular matrix (ECM) parameters, the HADR hydrogel achieves compatibility with the physiological mechanics of the human liver and fosters the adhesion and proliferation of multiple cell types. In vitro drug efficacy tests showed that HepG2 cell line-derived liver cancer organoids exhibited higher IC50 values than 2D cultures, indicating greater drug resistance. Subcutaneous tumor models in nude mice revealed that HADR hydrogels created a microenvironment for HepG2 cells mirroring the natural tumor ECM, leading to increased tumor volume, denser cell arrangement, and concurrent microvascular development. In vivo drug efficacy evaluations indicated that DOX treatment downregulated Ki-67 and MMP-9 expression, inhibiting HepG2 cell proliferation, invasion, and metastasis. These findings demonstrate the potential of HADR hydrogels for liver cancer organoid culture, offering new strategies for personalized drug screening and efficacy evaluation.

Sulfonated corn stalk enhanced hydrogel adsorption for heavy metal from metal mine gallery effluent

There are various of abandoned metal mines in China, and a considerable amount of heavy metal contaminated water is generated through water–rock interactions and accumulated within metal mine gallery. Therefore, the effective removal of heavy metals from metal mine gallery effluent holds significant importance. In this study, sulfonated corn stalk (SCS) and acrylic acid was used to prepare the double network hydrogel SCS-gel. The maximum allowable compression force for the SCS-gel was about 3 times than that of raw hydrogel. The SCS-gel exhibited a stable adsorption capacity within the pH range from 2.0 to 6.0. The maximal adsorption capacities of Pb2+ and Cu2+ on the SCS-gel were 111.6 and 370.2 mg/g, respectively. The functional groups of –OH, C-O, C = O, COOH, and −SO3- were participated in the adsorption process through coordination and electrostatic interactions. The SCS-gel exhibited promising reusability as the adsorption efficiency for Pb2+ and Cu2+ remained at approximately 100 % within 10 cycles of adsorption–desorption. The SCS-gel had an excellent removal efficiency for Pb2+ (99.8 %), Cu2+ (99.1 %), Mn2+ (97.4 %), Zn2+ (98.8 %), and Al3+ (95.7 %) from actual metal mine gallery effluent by dosage of 5 g/L with the initial concentrations of Pb2+, Cu2+, Mn2+, Zn2+, and Al3+ were 4.352, 29.20, 13.02, 7.016, and 30.47 mg/L, respectively. In the fixed-bed experiments, the Thomas model has a good description for the breakthrough curves of these heavy metals. These results confirmed the possibility of adopting SCS ethers for hydrogel fabrication and verified its great potential for the practical application for the removal of heavy metals from metal mine gallery effluent.

A high temperature-resistant, strong, and self-healing double-network hydrogel for profile control in oil recovery

Hydrogels are widely used in profile control to plug high-permeability zones in oil recovery. In this study, a novel double-network (DN) hydrogel is developed for profile control. The two networks of the prepared hydrogel are polyacrylamide (PAAm) crosslinked by N,N’-Methylenebisacrylamide (MBAA) and konjac glucomannan (KGM) crosslinked by borax (B), respectively. The two networks are interconnected by their interpenetrating structures and hydrogen bonds. Based on the results of a series of evaluation experiments, the AAm/KGM DN hydrogels developed in this study exhibit a strong mechanical strength with their fracture stresses exceeding 0.137 MPa. Meanwhile, the AAm/KGM DN hydrogels can remain thermally stable after being heated at 130 °C for 24 h, indicating the good high-temperature resistance of the new sample. Moreover, the prepared AAm/KGM DN hydrogels present excellent self-healing performance due to the abundant hydrogen bonds in their structures, which helps form stable and long-term plugging in porous media. In addition, the pure PAAm hydrogel and the AAm/KGM DN hydrogel are sheared into two dispersed particle gel (DPG) suspensions to investigate their plugging performances. The results demonstrate that the AAm/KGM DN DPG can effectively plug a high-permeability sandpack with a plugging efficiency of 93.2 %, while the pure AAm DPG can only provide a much lower plugging efficiency of 60.5 %. The AAm/KGM DN hydrogel developed in this study, with its high mechanical strength, high-temperature resistance, and self-healing capability, offers a promising new candidate for profile control in oil recovery.

Ag quantum dots-doped poly (vinyl alcohol)/chitosan hydrogel coatings to prevent catheter-associated urinary tract infections

The prevention of catheter-associated urinary tract infections (CAUTIs) significantly impacts the reduction of morbidity and mortality associated with the use of indwelling urinary catheters. This study focused on developing an antibacterial double network hydrogel coating for latex urinary catheters, which incorporated Ag quantum dots (Ag QDs) in a polyvinyl alcohol (PVA)-chitosan (CS) double network hydrogel matrix. The PVA-CS-Ag QDs, referred to as the PCA hydrogel coating exhibited excellent mechanical and physiochemical properties with controlled release of Ag QDs. The antibacterial properties of the PCA hydrogel-coated urinary catheters were studied against both gram-negative Escherichia coli (E. coli, ATCC25922) and gram-positive Staphylococcus aureus (S. aureus, ATCC29213). The continuous release of CS oligomers and Ag QDs from the hydrogel coating contributed to the synergistic antibacterial and antiadhesion effects. Measurements of the Ag release rate revealed that even after 30 days, the concentration of Ag QDs from the PCA hydrogel-coated urinary catheters remained significantly higher than the effective antibacterial concentration of the total Ag (0.1 μg·L−1). These results indicated that the PCA hydrogel coating not only efficiently prevented bacteria attachment, but also exhibited long-term antibacterial activity, thereby inhibiting biofilm formation. Furthermore, the PCA hydrogel-coated urinary catheter demonstrated excellent biocompatibility and hemocompatibility. Overall, this novel PCA hydrogel-coated urinary catheter, with its exceptional antibacterial properties, holds great potential in reducing the incidence of CAUTIs.

Developing biomimetic PVA/PAA hydrogels with cellulose nanocrystals inspired by tree frog structures for superior wearable sensor functionality

This study developed a wearable sensor device featuring biomimetic structures inspired by tree frog toe pads to measure shoulder joint movements effectively. A PVA/PAA double-network hydrogel was formulated by mixing PVA and PAA in a 3:7 ratio, resulting in a Young's modulus of 7.2 kPa, closely matching human skin's mechanical properties. To enhance moisture retention, the hydrogel was supplemented with 20 mL glycerin, increasing its weight retention rate to 95 % after 28 days, a 5.6-fold improvement over glycerin-free hydrogels. Additionally, the incorporation of 0.2 wt% cellulose nanocrystals (CNC) increased the cross-linking density, reducing the swelling ratio from 124 % to 106 % and minimizing the impact of swelling cycles on mechanical properties from 22 % to 4 %. Treefrog-inspired microstructures were fabricated on the sensor surface using laser cutting and casting techniques, significantly enhancing adhesion under humid conditions, with normal, lateral, and peel-off adhesion forces improving by 500, 700, and 700 %, respectively. The sensor demonstrated accurate measurement of shoulder joint movements with an error margin of 6.3 % for polar angles (45°-135°) and 7.8 % for azimuth angles (0°-45°). The accompanying smartphone application provided real-time feedback, helping to prevent exercise injuries and improve user awareness and control of shoulder movements, making it suitable for both rehabilitation and athletic training.

MXene and cellulose nanofibers reinforced hydrogel with high strength and photothermal self-healing performances for marine antifouling

Biological fouling is a considerable threat to the marine industry because attached microcontaminants and microorganisms inflict serious damage on marine installations and aquacultures. Although there has been tremendous effort in researching marine antifouling, it is yet challenging to develop a long-term and consistent antifouling strategy and materials. Here, polyhexamethylene-biguanide (PHMB) and MXene are introduced into the carboxylated cellulose nanofibers (CNF) reinforced polyvinyl alcohol (PVA) hydrogel to obtain a self-healing and ultra-high toughness antifouling hydrogel. The as-prepared double network (DN) hydrogels have extremely high toughness (16,050 kJ/m3), superior anti-protein adhesion (100 %) and anti-algal adhesion (100 %), exceptional antibacterial activity (99.97 %), and remarkable photothermal self-healing capability. Furthermore, the DN hydrogel provide outstanding antifouling performance for at least six months in the actual marine field. This work provides an effective and feasible strategy to prevent marine biofouling and also initiates new approaches to the application of hydrogel.

Congelation- and dehydration-tolerant, mechanically robust hydrogel electrolyte for durable iontronic sensors operating in open air and freezing temperatures over wide strain and pressure ranges

Conventional hydrogels have limitations in mechanical properties and are susceptible to loss of elasticity and conductivity caused by congelation and dehydration, limiting their practical uses for application in high-stress environments, open air, and freezing temperatures. This study introduces a mechanically robust, dehydration- and congelation-tolerant, and ionically conductive hydrogel electrolyte, practical for iontronic sensors working in wide pressure and strain ranges under open-air and freezing temperatures. This hydrogel electrolyte is fabricated through a reconstruction process comprising a drying-induced densification of double-network hydrogel of alginate and polyacrylamide, a structure fixation by Fe3+ crosslinking, and a Li+ infiltration. The resultant hydrogel electrolyte is tolerant to dehydration and congelation and mechanically robust, with strength and elastic modulus of a few mega-pascals comparable to those of non-conductive elastomers/rubbers used as dielectric materials. Therefore, the hydrogel electrolyte-based iontronic sensors demonstrate exceptional sensitivity and stability under compression and tension and across a wide temperature range. Further, the sensor demonstrates their practical applicability in high-stress environments from kg-range human weight to ton-range car weight. These achievements evince that iontronic sensors, based on mechanically robust and ionically conductive hydrogel electrolytes tolerant to congelation and dehydration, can be employed for practical applications.

Super-Tough, Non-Swelling Zwitterionic Hydrogel Sensor Based on the Hofmeister Effect for Potential Motion Monitoring of Marine Animals.

Hydrogel-based electronic devices in aquatic environments have sparked widespread research interest. Nevertheless, the challenge of developing hydrogel electronics underwater has not been profoundly surmounted because of the fragility and swelling of hydrogels in aquatic environments. In this work, a zwitterionic double network hydrogel comprisedof polyvinyl alcohol (PVA), poly(sulfobetaine methacrylate) (PSBMA), and sulfuric acid (H2SO4) demonstrates super-tough and non-swelling performance. The Hofmeister effect of H2SO4 and PSBMA induces the PVA chains to form numerous nanocrystalline domains, which serve as the primary physical crosslinking points and provide effective energy dissipation. H2SO4 induces a strong salting-out effect to facilitate PVA crystallization and the formation of a dense and stable network structure that inhibits swelling. The resulting hydrogel exhibits an ultra-high toughness of 4.61MJm-3, non-swelling, and long-term stability for up to a month in pure water and seawater. Based on this, a hydrogel-based seawater strain sensor has been developed to monitor the underwater movements of marine animal models. Reliable and stable sensing performance ensures real-time collection of underwater motion signals, despite the impacts of water flow and the interference of ions. This study provides a facile approach to designing super-tough and non-swelling hydrogels and further expands the application of underwater electronic devices.

Preparation and application of organic hydrogels incorporating polyacrylamide/sodium alginate/DMSO for enhanced anti-drying, anti-freezing, and self-healing properties

The double-network hydrogel comprises two asymmetrically structured cross-linked networks, demonstrating exceptional mechanical properties and possessing significant potential for application in the field of flexible sensors. However, conventional hydrogels primarily disperse in water as a medium and continuously lose moisture in natural environments, rendering them incapable of retaining hydration over extended periods and unsuitable for utilization under low-temperature conditions. In this study, we devised an organic hydrogel based on polyacrylamide (PAM), sodium alginate (SA), and dimethyl sulfoxide (DMSO). Through hydrogen bonding interactions among DMSO molecules, polyacrylamide, and sodium alginate, this organic hydrogel not only exhibits anti-drying and anti-freezing properties but also demonstrates self-healing characteristics. Moreover, the organic hydrogel showcases remarkable mechanical properties and conductivity capabilities that render it suitable for constructing flexible strain sensors to monitor human movements such as finger bending, elbow flexion, knee joint bending, and ankle extension. Additionally, the sensor exhibits excellent stability and durability.

Preparation of a chitosan/polyvinyl alcohol-based dual-network hydrogel for use as a potential wound-healing material for the sustainable release of drugs

Treating chronic wounds poses significant challenges in clinical medicine due to bacterial infection, reactive oxygen species (ROS) accumulation, and excessive inflammation. This study aimed to address these issues by developing a wound dressing with antibacterial, antioxidant, and anti-inflammatory properties. Chitosan was functionally modified with acrolein to covalently bind to epigallocatechin gallate (EGCG), enabling a high EGCG load. Subsequently, polyvinyl alcohol (PVA) and EGCG-modified chitosan were crosslinked to prepare a new double-network hydrogel with added cysteine (CSAEC/P50). CSAEC/P50 demonstrated optimal mechanical properties (low swelling rate, high water retention, and optimal flexibility), low hemolysis, high coagulation properties, and antibacterial and antioxidant activities. Cell scratch tests indicated that CSAEC/P50 can promote NIH3T3 cell migration. Immunofluorescence results showed that CSAEC/P50 promoted the transformation of proinflammatory M1 macrophages to anti-inflammatory M2 macrophages. These findings suggest that CSAEC/P50 has significant potential for use in wound dressing applications.

Exploring performance and mechanism of modified metal-organic frameworks in calcium alginate/polyvinyl alcohol double-network hydrogels for effective dye wastewater treatment

To address the growing problem of dye wastewater pollution, a novel MOFs adsorbent calcium alginate/polyvinyl alcohol@UiO-66 was developed using environmentally friendly polymers, sodium alginate and polyvinyl alcohol creating gel spheres with a double-network structure through cross-linking. UiO-66 metal-organic frameworks are then grown onto the gel spheres, resulting in the final CA/PVA@UiO-66 adsorbent. This adsorbent boasts a high surface area (17.4 m2/g) and a mesoporous-nested microporous structure. It effectively removes MB from water, the actual maximum adsorption capacity was measured at 275.8 mg/g, which surpasses most existing adsorbents. Remarkably, the adsorbent retains 93.9 % of its initial capacity even after 10 reuse cycles. The adsorption process adhered to the Redlich-Peterson model and the PFO model. The N2-Sorption isotherm, actual Methylene blue (MB) adsorption experiments, and model analysis further suggest that the adsorption process is a complex heterogeneous diffusion process involving simultaneous chemical and physical adsorption. Additionally, the adsorption process is endothermic, indicating that it can occur spontaneously at 298 K. Increasing the temperature promotes the forward progress of the adsorption reaction, thereby enhancing the adsorption capacity. The gel adsorbent exhibited excellent dye wastewater purification capabilities, coupled with commendable reusability.

Constructing Mg-phytic acid enhanced hydrogel patch with janus structure for antibacterial and angiogenic urethral repair

Due to bacteria in urine and inadequate blood supply, urethral defect repair faces great clinical difficulties. Inspired by the natural structure of the urethra, in this study, we designed a multifunctional hydrogel urethral patch with a Janus structure. The inner layer was a double-network hydrogel of polyvinyl alcohol/carboxymethyl chitosan (PVA/CMCS) enhanced by natural phytic acid (PA) and Mg2+ (Mg2+-PA/PVA/CMCS). The outer layer was composed of poly (L-lactic acid) (PLLA) nanofibers to form a hydrophobic barrier, coupling via a micelle layer to ensure interfacial bonding. The patch exhibited mechanical properties matching soft tissues, with maximum tensile strength and toughness of 1.69±0.13 MPa and 24.7±0.9 MJ/m3, respectively, under the strengthening effect of Mg2+-PA chelation. Therein, the 4 % Mg2+-PA/PVA/CMCS composite patch could maintain unilateral hydrophobicity for at least 14 days and demonstrated an antibacterial rate of 99.0 %±0.1 % against E. coli. In PBS, the patch could deliver Mg2+ for at least 7 days and stabilize the surrounding pH environment for up to 28 days. In vitro cell experiments indicated that the 4 % Mg2+-PA/PVA/CMCS composite patch could promote the human umbilical vein endothelial cell (HUVEC) proliferation and migration, with the angiogenic protein expression enhanced more than 1.2 times compared with the Control group. In conclusion, the patch constructed in this study may provide a new approach to clinical urethral injury repair.

Sweat-Enhanced Self-Adhesive Double-Network Hydrogel for Dynamic Skin Electrophysiology

Sweat-Enhanced Self-Adhesive Double-Network Hydrogel for Dynamic Skin Electrophysiology