Repeatable Adhesion Research Articles

Motion-Adaptive Tessellated Skin Patches With Switchable Adhesion for Wearable Electronics.

Skin-interfaced electronics have emerged as a promising frontier in personalized healthcare. However, existing skin-interfaced patches often struggle to simultaneously achieve robust skin adhesion, adaptability to dynamic body motions, seamless integration of bulky devices, and on-demand, damage-free detachment. Here, a hybrid strategy that synergistically combines these critical features within a thin, flexible patch platform is introduced. This design leverages shape memory polymers (SMPs) arranged in a tessellated array, comprising both rigid and compliant SMPs. This configuration enables exceptional deformability, motion adaptability, and ultra-strong, repeatable skin adhesion while offering on-demand adhesion control. Furthermore, the design facilitates the seamless integration of bulky electronics without compromising skin adhesion. By incorporating sizeable electronics including signal acquisition circuits, sensors, and a battery, it is demonstrated that the proposed tessellated patch can be securely mounted on the skin, accommodate dynamic body motions, precisely detect physiological signals with an outstanding signal-to-noise ratio (SNR), wirelessly transmit data, and be effortlessly released from the skin.

Environmentally stable and rapidly polymerized tin-tannin catalytic system hydroxyethyl cellulose hydrogel for wireless wearable sensing

In recent years, flexible sensors constructed mainly from hydrogels have played an indispensable role in several fields. However, the traditional hydrogel preparation process involves complex and time-consuming steps and the freezing or volatilization of water in the water gel in extreme environments greatly limits the further use of the sensor. Therefore, an ionic conductive hydrogel (SnHTD) was designed, which was composed of tannic acid (TA), metal ions Sn2+, hydroxyethyl cellulose (HEC), and acrylamide (AM) in a deep eutectic solvent (DES) and water binary solvent. It is worth noting that the gel time is shortened to less than 3 min by introducing the Sn-TA redox system. The addition of DES makes the hydrogel have a wide temperature tolerance range (−20 to 60 °C) and the ability to store for a long time (30 days). The introduction of HEC increased the tensile stress of hydrogel from 140.17 kPa to 219.89 kPa. Additionally, the hydrogel also has high conductivity, repeatable adhesion and UV shielding properties. In general, this research opens up a new way for room temperature polymerization of environmentally resistant hydrogel materials and effectively meets the growing demand for wireless wearable sensing.

Freezing-Tolerant Supramolecular Adhesives from Tannic Acid-Based Low-Transition-Temperature Mixtures.

Natural polyphenols like tannic acid (TA) have recently emerged as multifunctional building blocks for designing advanced materials. Herein, we show the benefits of having TA in a dynamic liquid state using low-transition-temperature mixtures (LTTMs) for developing freezing-tolerant glues. TA was combined with betaine or choline chloride to create LTTMs, which direct the self-assembly of guanosine into supramolecular viscoelastic materials with high adhesion. Molecular dynamics simulations showed that the structural properties of the material are linked to strong hydrogen bonding in TA-betaine and TA-choline chloride mixtures. Notably, long-term and repeatable adhesion was achieved even at -196 °C due to the binding ability of TA's catechol and gallol units and the mixtures' glass transition temperature. Additionally, the adhesives demonstrated injectability and low toxicity against fibroblasts in vitro. These traits reveal the potential of these systems as bioadhesives for tissue repair, opening new avenues for creating multifunctional soft materials with bioactive properties.

Tough, self-healing, adhesive double network conductive hydrogel based on gelatin-polyacrylamide covalently bridged by oxidized sodium alginate for durable wearable sensors

Pursuing high-performance conductive hydrogels is still hot topic in development of advanced flexible wearable devices. Herein, a tough, self-healing, adhesive double network (DN) conductive hydrogel (named as OSA-(Gelatin/PAM)-Ca, O-(G/P)-Ca) was prepared by bridging gelatin and polyacrylamide network with functionalized polysaccharide (oxidized sodium alginate, OSA) through Schiff base reaction. Thanks to the presence of multiple interactions (Schiff base bond, hydrogen bond, and metal coordination) within the network, the prepared hydrogel showed outstanding mechanical properties (tensile strain of 2800 % and stress of 630 kPa), high conductivity (0.72 S/m), repeatable adhesion performance and excellent self-healing ability (83.6 %/79.0 % of the original tensile strain/stress after self-healing). Moreover, the hydrogel-based sensor exhibited high strain sensitivity (GF = 3.66) and fast response time (<0.5 s), which can be used to monitor a wide range of human physiological signals. Based on this, excellent compression sensitivity (GF = 0.41 kPa−1 in the range of 90–120 kPa), a three-dimensional (3D) array of flexible sensor was designed to monitor the intensity of pressure and spatial force distribution. In addition, a gel-based wearable sensor was accurately classified and recognized ten types of gestures, achieving an accuracy rate of >96.33 % both before and after self-healing under three machine learning models (the decision tree, SVM, and KNN). This paper provides a simple method to prepare tough and self-healing conductive hydrogel as flexible multifunctional sensor devices for versatile applications in fields such as healthcare monitoring, human-computer interaction, and artificial intelligence.

A novel multifunction of wearable ionic conductive hydrogel sensor for promoting infected wound healing

Conductive hydrogels have attracted widespread attention in applications of artificial biological tissues and ionic skin. Herein, a highly ionically conductive and biocompatibility hydrogels that integrate sensing, low swelling, and antimicrobial are prepared by the composition of chitosan (CS) chains, tannic acid (TA), polyacrylic acid (PAA), and metal cations. The hydrogels with high conductivity had tensile strain repeatable adhesion, wide strain detection, biocompatibility, and motion sensing capabilities. Particularly, in the aspect of hydrogel strain sensing based on ion conduction, it has high nonliearity (GF=2.05) with a large strain (20 %-1400 %), and excellent cycle stability. In addition, owing to the low-swelling effect and dipole-dipole interaction between the existence of free catechol groups of the zwitterionic group and TA in the zwitterionic sulfobetaine methacrylate (SBMA), the hydrogels display repeatable and controllable adhesiveness. Meanwhile, the covalent cross-linking between AA and SBMA synergistically enhances the mechanical properties of the hydrogels (169 kPa, 1474 %). Furthermore, as demonstrated in the L929 mouse wound infection model, the results indicated that the prepared hydrogel group had antimicrobial activity and reduced inflammation, thereby accelerating wound healing. The biocompatible and mutli-functional conductive hydrogels provide a new method for the design of novel type ionic skin device.

A reusable, healable, and biocompatible PEDOT:PSS hydrogel-based electrical bioadhesive interface for high-resolution electromyography monitoring and time–frequency analysis

As the most ideal interface between bioelectronic devices and biological tissues, the electrical bioadhesive interface (EBI) holds significant potential for various applications, including soft bioelectronics, wearable devices, and electrophysiological signal monitoring. However, most current EBIs are disposable products that lack repeatable adhesion and self-healing properties, thus hindering practical applications. Herein, we develop a reusable EBI by incorporating a dynamic non-covalent interaction enhancer polydopamine (PDA) and conductive PEDOT:PSS into an adhesive hydrogel matrix polyacrylamide (PAM). The EBI exhibits intriguing overall electrical and mechanical properties, including high conductivity (5.57 S m−1), tissue-like Young’s modulus (2.7 kPa), low interfacial impedance (1 kΩ), and excellent adhesion strength (46.45 ± 1.75 kPa on porcine skin) with excellent retention (87 %) after 200 adhering/detaching cycles, high self-healing efficiency of 94.11 %, and outstanding biocompatibility in HDF-a and HaCaT cell models. Benefiting from these superior properties, we further demonstrate the fabrication and application of an EBI-based reusable electromyography monitoring patch (EMP). The reusable EMP enables high-resolution electromyography signal monitoring capability with a higher signal-to-noise ratio (SNR) of 30.05 dB than commercial electrodes (12.06 dB). Remarkably, such reusable EMP maintains very stable SNR of 21.82 dB after 200 adhering/detaching cycles (3.8 times higher than commercial electrodes, 5.74 dB after 30 cycles), and showcases typical time and frequency-domain characteristics. These findings demonstrate a promising reusable EMP to enhance the accuracy and convenience of electromyography monitoring.

Repeatable adhesion of bio-based polymer derived from tetrafunctional epoxides and polyhydric carboxylic acid

Bio-based network polymers were synthesized by cross-linking diastereomeric tetrafunctional epoxides, tetra-trans-LO (1) and tetra-cis-LO (2), with polyhydric carboxylic acid in the presence and absence of a catalyst. The cross-linking ability of 1 was higher than that of 2 and afforded to higher polymer yields, thermal stability, and mechanical strength. Repeatable adhesion with a moderately high recovery strength was achieved using 1 and polyhydric carboxylic acid in the presence of Zn(acac)2.

Ultra-stretchable and highly tough ionogels with underwater repeatable adhesion and anti-swelling capacity for real-time motion detection, signal transmission and electrochemical monitoring platforms

Hydrophobic ionogels have received growing interest as a flexible underwater sensing material. However, it remains a significant challenge to improve the tensile properties, prolonged underwater repeatable adhesion, and multifunctionality of the hydrophobic ionogel due to the restricted selection of monomers and curing strategies. Herein, a hydrophobic multifunctional fluorine-rich ionogel with ultra-stretchability and superior long-term underwater repeatable adhesion is designed by virtue of the introduction of a rigid and flexible macromolecular cross-linker and a structure of rigid cationic imidazole-benzene rings in a hydrophobic ionic liquid monomer. The macromolecular cross-linker significantly improves the mechanical properties of the ionogel because of the reduction in stress concentration. And the structure of short imidazole-benzene rings with high rigidity exposes a larger amount of adhesion groups on the surface of the ionogels compared to the flexible groups, leading to enhanced long-term underwater repeatable adhesion performance of the ionogel. The ionogels are applied to real-time monitoring of exposure to water, underwater swimming motion monitoring, underwater Morse code transmission and electrochemical monitoring platforms. And this work is expected to provide ideas for the multifunctionalization of underwater sensing technology and the integration of functional units in underwater flexible electronic skin.

High‐Adhesion, Weather Resistance, Reusable PAM/Gly/Gel/TA/Fe3+ Biopolymer Dual‐Network Conductive Hydrogel for Flexible Bioelectrode

AbstractConductive hydrogel is considered a promising wearable sensor material. Developing flexible conductive hydrogel sensors with stretchability, adhesion, and stability remains challenging. In this study, a transparent, self‐adhesive, antifreeze, anti‐UV, stretchable, conductive, and reusable hydrogel with polyacrylamide/glycerol/gelatin/tannic acid/Fe3+ (PGGT‐Fe3+) structure is successfully constructed through a simple one‐pot polymerization method. The PGGT‐Fe3+ hydrogel is composed of dual networks of polyacrylamide and gelatin for organic cross‐linking, using water/glycerol as the dispersion medium, and incorporates a viscous substance: tannic acid, and a conductive substance: metal ions (Fe3+). Due to the introduction of the abundant amino, carboxylic acid, and hydroxyl functional groups on gelatin and tannic acid, the PGGT‐Fe3+ hydrogel exhibits excellent and repeatable adhesion capabilities on various surfaces (including glass, metal, plastic, and pigskin) with maximum adhesion strength of 98 kPa when attached to pigskin. Furthermore, based on the stable conductive network and high conductivity, the hydrogel not only exhibits strain sensitivity, fast response, and stability but also can stably collect epidermal bio signals. In conclusion, this work provides a new approach to the design and development of next‐generation multifunctional conductive hydrogels and opens up vast possibilities for their applications in the flexible electronics field.

Multifunctional Conductive Double-Network Hydrogel Sensors for Multiscale Motion Detection and Temperature Monitoring.

As typical soft materials, hydrogels have demonstrated great potential for the fabrication of flexible sensors due to their highly compatible elastic modulus with human skin, prominent flexibility, and biocompatible three-dimensional network structure. However, the practical application of wearable hydrogel sensors is significantly constrained because of weak adhesion, limited stretchability, and poor self-healing properties of traditional hydrogels. Herein, a multifunctional sodium hyaluronate (SH)/borax (B)/gelatin (G) double-cross-linked conductive hydrogel (SBG) was designed and constructed through a simple one-pot blending strategy with SH and gelatin as the gel matrix and borax as the dynamic cross-linker. The obtained SBG hydrogels exhibited a moderate tensile strength of 25.3 kPa at a large elongation of 760%, high interfacial toughness (106.5 kJ m-3), strong adhesion (28 kPa to paper), and satisfactory conductivity (224.5 mS/m). In particular, the dynamic cross-linking between SH, gelatin, and borax via borate ester bonds and hydrogen bonds between SH and gelatin chain endowed the SBG hydrogels with good fatigue resistance (>300 cycles), rapid self-healing performance (HE (healing efficiency) ∼97.03%), and excellent repeatable adhesion. The flexible wearable sensor assembled with SBG hydrogels demonstrated desirable strain sensing performance with a competitive gauge factor and exceptional stability, which enabled it to detect and distinguish various multiscale human motions and physiological signals. Furthermore, the flexible sensor is capable of precisely perceiving temperature variation with a high thermal sensitivity (1.685% °C-1). As a result, the wearable sensor displayed dual sensory performance for temperature and strain deformation. It is envisioned that the integration of strain sensors and thermal sensors provide a novel and convenient strategy for the next generation of multisensory wearable electronics and lay a solid foundation for their application in electronic skin and soft actuators.

Reusable and Porous Skin Patches with Thermopneumatic Adhesion Control Capability and High Water Vapor Permeability.

We present a reusable and porous skin patch (RPS patch) capable of controlling adhesion force with a thermal-pneumatic method for repetitive use as well as improving moisture permeability for long-term use without skin troubles. Previous skin patches cause skin troubles due to high adhesion force (∼30 kPa) and low moisture permeability (∼382 g/m2/day), hindering them from repeatable and long-term use. We control the skin adhesion force of the RPS patch using thermopneumatic pressure generated by an embedded heater on multiple chamber arrays. The RPS patch controls the adhesion force ranging from 8 to 29 kPa on both dry and wet skin while keeping the stable adhesion force for 48 h. It shows repeatable adhesion up to 100 times, and the adhesion force is restored after the RPS patch is washed with water, thus enabling repetitive skin adhesion. We improve the moisture permeability of the RPS patch to 733 g/m2/day while maintaining the adhesion force by making the RPS patch with porous materials. The RPS patch shows no skin troubles for 7 days of attachment, thereby being available for long-term skin attachment. The RPS patch, having adhesion control capability and high moisture permeability, shows potential for use in daily life in biomedical applications, including wearable sensors, medical adhesives, and rehabilitation robots.

Designing directional adhesive pillars using deep learning-based optimization, 3D printing, and testing

Nature-inspired fibrillar adhesives have versatile applications, such as wall-climbing robots and grippers, which require residue-free and repeatable adhesion. To meet the requirements of excellent adhesion strength combined with controllability of adhesion and detachment, directional adhesive pillars with anisotropic adhesion properties have been extensively investigated. However, existing designs that simply mimic nature suffer from relatively weak adhesion and insufficient directionality, because most of them were designed without considering a sufficiently large design space. In this study, we rigorously defined adhesive directionality and systematically investigated the optimal pillar shape to obtain an excellent combination of adhesion strength and directionality using deep-learning-based optimization. A data-driven model based on artificial neural networks was trained using finite element analysis data obtained from 199,466 adhesive pillar shapes, which can predict the directionality and adhesion strength of given pillar shapes. Optimization was performed using the trained neural network to obtain the optimal pillar shape under the geometric constraints necessary to secure the reliability of the pillar. Finally, we suggest adhesive pillar shapes having severe directionality and high adhesive strength at the same time. For validation of our optimization model and optimized result, the proposed pillar shapes were fabricated using a 3D polyjet printer, and their adhesion strength and directionality were tested. We noticed that optimized pillar shapes we obtained have superior directionality and adhesion strength in real.

Lignin-induced rapid-synthesis of deep eutectic solvent-based gel with high robustness and conductivity applied for flexible quasi-solid-state supercapacitors

A novel rapid-synthesis method for the preparation of high-performance deep eutectic solvent (DES)-based gel was proposed for constructing flexible quasi-solid-state supercapacitors. The dynamic redox reaction between silver ions and lignin produced large amounts of free radicals, which triggered the polymerization of acrylic acid monomer (AA) to form silver-lignin nanoparticle/DES/Poly (acrylic acid) (Ag-L NPs/DES/PAA) composite gel. Ag-L NPs constructed a dynamic redox system that generated catechol groups, triggering rapid self-gelation of Ag-L NPs/DES/PAA at room temperature, while imparting long-term and repeatable adhesion ability to the hydrogel. In addition, DES, as the liquid component of Ag-L NPs/DES/PAA, not only provided a good solution system for lignin but also enhanced its electrochemical performance and stability. Thanks to the synergistic effects of DES and the dynamic transformation of lignin and silver, Ag-L NPs/DES/PAA not only exhibited a high conductivity of over 10 mS/cm, but also showed a remarkable adhesion strength of over 80 KPa. Moreover, the presence of lignin endowed Ag-L NPs/DES/PAA with more than 300% strain and over 350 KPa compression performance. A supercapacitor based on this assembly exhibited a high specific capacitance (208F g−1, 0.5 A g−1) and an impressive capacity retention rate of 92.05% after 3000 cycles. This research offered insightful information on the use of lignin in flexible electronics.

Ultrasound-triggered piezocatalytic composite hydrogels for promoting bacterial-infected wound healing.

Wound healing has become one of the basic issues faced by the medical community because of the susceptibility of skin wounds to bacterial infection. As such, it is highly desired to design a nanocomposite hydrogel with excellent antibacterial activity to achieve high wound closure effectiveness. Here, based on ultrasound-triggered piezocatalytic therapy, a multifunctional hydrogel is designed to promote bacteria-infected wound healing. Under ultrasonic vibration, the surface of barium titanate (BaTiO3, BT) nanoparticles embedded in the hydrogel rapidly generate reactive oxygen species (ROS) owing to the established strong built-in electric field, endowing the hydrogel with superior antibacterial efficacy. This modality shows intriguing advantages over conventional photodynamic therapy, such as prominent soft tissue penetration ability and the avoidance of serious skin phototoxicity after systemic administration of photosensitizers. Moreover, the hydrogel based on N-[tris(hydroxymethyl)methyl]acrylamide (THM), N-(3-aminopropyl)methacrylamide hydrochloride (APMH) and oxidized hyaluronic acid (OHA) exhibits outstanding self-healing and bioadhesive properties able to accelerate full-thickness skin wound healing. Notably, compared with the widely reported mussel-inspired adhesive hydrogels, OHA/THM-APMH hydrogel due to the multiple hydrogen bonds from unique tri-hydroxyl structure overcomes the shortage that catechol groups are easily oxidized, giving it long-term and repeatable adhesion performance. Importantly, this hybrid hydrogel confines BT nanoparticles to wound area and locally induced piezoelectric catalysis under ultrasound to eradicate bacteria, markedly improving the therapeutic biosafety and exhibits great potential for harmless treatment of bacteria-infected tissues.

Scale-Spanning Strong Adhesion Using Cellulose-Based Microgels.

Adhesive gels derived from biobased sustainable materials have extremely broad application prospects, such as in flexible smart materials and biomedicine fields. Combining high toughness and strong, persisting repeatable adhesion has always been a daunting challenge for adhesive gels. However, bulk gels based on polysaccharides as the most abundant bio-based compounds usually possess a high toughness but weak interfacial adhesion due to the strong hydration potential. Herein, a novel kind of highly tough microgel membranes with rough surfaces is fabricated using loosely chemically cross-linked dihydroxypropyl cellulose (cDHPC) microgels (average size = 1.25±0.03µm). Such microgel membranes exhibit strong, instant, and persisting adhesion to various substrates with different surface roughness. Slight chemical cross-linking and multiple physical interactions within microgels and resulting microgel membranes lead to high tensile strength and toughness of 0.23±0.03MPa and 73.8±9.3KJm-3 , respectively. The maximum adhesive strength and debonding work exceed 320±0.50KPa and 160.97±0.20Jm-2 , respectively. After five cycles (re-lap after detaching), the adhesive strength still remains above 200 KPa. Their adhesive properties outperform most bio-based adhesive gels and even petroleum-based gels, which are based on synergistic molecular and microscaled topological interactions.

Hydrogel transformed from sandcastle-worm-inspired powder for adhering wet adipose surfaces

Normally, hydrogel adhesives do not perform well on adipose matters that are covered with bodily fluids. Besides, the maintenance of high extensibility and self-healing ability in fully swollen state still remains challenging. Based on these concerns, we reported a sandcastle-worm-inspired powder, which was made of tannic acid-functionalized cellulose nanofiber (TA-CNF), polyacrylic acid (PAA) and polyethyleneimine (PEI). The obtained powder can rapidly absorb diverse bodily fluids and transform into a hydrogel, displaying fast (＜3 s), self-strengthening and repeatable wet adhesion to adipose tissues. Due to the dense physically cross-linked network, the formed hydrogel still showed excellent extensibility (∼14 times) and self-healing ability after being immersed in water. Moreover, excellent hemostasis, antibacterial ability and biocompatibility make it suitable for numerous biomedical applications. With combined advantages of powders and hydrogels, such as good adaptability to irregular sites, efficient drug loading capacity and tissue affinity, the sandcastle-worm-inspired powder offers significant promise as tissue adhesive and repair materials. This work may open new avenues for designing high-performance bioadhesives with efficient and robust wet adhesiveness to adipose tissues.

A highly stretchable, fast self-healing elastomer with fast, tough, repeatable adhesion

Integration of high toughness, fracture resistance, and fast self-healing, as well as robust adhesion is critically required for flexible electronics, healthcare monitoring, and electronic skins. However, it still remains a critical challenge to combine these significant functions into one material. Here, we synthesize an elastomer by copolymerizing two acrylate monomers containing functional groups and established hierarchical dipolar interactions and hydrogen bonds between C-F, C=O, -O-CH3, and C-H groups with different bonding strengths, which successfully not only combines with high toughness (31.41 ± 1.12 MJ m−3), outstanding crack resistance (fracture energy: 10252 ± 208 J m−2), fast self-healing (completely restore within 30 min at room temperature), but also with fast, repeatable, and toughness adhesion to different substrates, e.g. PMMA, Aluminum, glass, steel, and PTFE. The PF4M6 demonstrates great sensing performance in detecting human motion. Overall, this work provides some insights for preparing high-performance, healing, and adhesive elastomer materials applied in electronics, adhesives, and interface materials.

Polymerizable rotaxane hydrogels for three-dimensional printing fabrication of wearable sensors

While hydrogels enable a variety of applications in wearable sensors and electronic skins, they are susceptible to fatigue fracture during cyclic deformations owing to their inefficient fatigue resistance. Herein, acrylated β-cyclodextrin with bile acid is self-assembled into a polymerizable pseudorotaxane via precise host-guest recognition, which is photopolymerized with acrylamide to obtain conductive polymerizable rotaxane hydrogels (PR-Gel). The topological networks of PR-Gel enable all desirable properties in this system due to the large conformational freedom of the mobile junctions, including the excellent stretchability along with superior fatigue resistance. PR-Gel based strain sensor can sensitively detect and distinguish large body motions and subtle muscle movements. The three-dimensional printing fabricated sensors of PR-Gel exhibit high resolution and altitude complexity, and real-time human electrocardiogram signals are detected with high repeating stability. PR-Gel can self-heal in air, and has highly repeatable adhesion to human skin, demonstrating its great potential in wearable sensors.

Collagen-Based Organohydrogel Strain Sensor with Self-Healing and Adhesive Properties for Detecting Human Motion.

Conductive hydrogels are ideal for flexible sensors, but it is still a challenge to produce such hydrogels with combined toughness, self-adhesion, self-healing, anti-freezing, moisturizing, and biocompatibility properties. Herein, inspired by natural skin, a highly stretchable, strain-sensitive, and multi-environmental stable collagen-based conductive organohydrogel was constructed by using collagen (Col), acrylic acid, dialdehyde carboxymethyl cellulose, 1,3-propylene glycol, and AlCl3. The resulting organohydrogel exhibited excellent tensile (strain >800%), repeatable adhesion (>10 times), self-healing [self-healing efficiency (SHE) ≈ 100%], anti-freezing (-60 °C), moisturizing (>20 d), and biocompatible properties. This organohydrogel also possessed good electrical conductivity (σ = 3.4 S/m) and strain-sensitive properties [GF (gauge factor) = 13.65 with the maximal strain of 400%]. Notably, the organohydrogel had a considerable low-temperature self-healing performance (SHE = 88% at -24 °C) and rapid underwater self-healing property (SHE = 92%, self-healing time <20 min). This type of strain sensor could not only accurately and continuously monitor the large-scale motions of the human body but also provide an accurate response to the human tiny motions. This work not only proposes a development strategy for a multifunctional conductive organohydrogel with multiple environmental stability but also provides potential research value for the construction of biomimetic electronic skin.

Dual-crosslinked bioadhesive hydrogel as NIR/pH stimulus-responsiveness platform for effectively accelerating wound healing

Adhesive hydrogels have emerged as promising candidates to solve life-threatening infectious skin injuries. However, the inadequate mechanical characteristics and biological adherence limit the traditional wound dressing unable to adapt to high-frequency movement and real-time monitoring of wound healing, calling for the development of bioadhesive materials guided wound healing. In this work, a multifunctional bioadhesive hydrogel with double colorimetric-integrated of polyethylene glycol (PVA)-dextran (Dex)-borax-bromothymol blue (BTB)-fluorescein thiocyanate (FITC) and functionalization by tungsten disulfide-catechol nanozyme (CL/WS2) was created. Hydrogel is a perfect biological adhesive, which can achieve repeatable and strong tissue adhesion strength (8.3 ± 0.6 kPa), which is 1.66 times that of commercial dressings. Based on the strong biological adhesion of the hydrogel, a sensor is integrated into the hydrogel to collect visual image of bacterial infection from a smartphone and transform it into an on-site pH signal for remote evaluation of the wound's dynamic status in real time. Ultimately, the adhesiveness hydrogel has high worth in managing the burden related to wound healing and paving the way for intelligent wound management in the future.