Adhesive Hydrogel Research Articles

Sweat-enhanced adhesive hydrogel enables interfacial exchange coupling for wearable strain sensor

PVA-based wearable hydrogels have emerged as promising candidate for motion sensors due to their skin-like softness and unique biocompatibility. However, an open question is whether and how the strain-sensitive hydrogel designing can prevent adhesive performance loss caused by sweat between devices and human-skin and reduce interfacial failure. Herein, a versatile sweat-enhanced adhesive hydrogel-based motion sensor (VDBA) paradigm is engineered consisting of sweat sensitivity and self-adhesive function components. Taking advantage of catechol chemistry inspired mussel, the VDBA hydrogel enhances substrate adhesion behavior. The borate ions (B(OH)4−) are found to efficient condensation form borate ester groups with phenolic hydroxyl. Interestingly, human sweat pH serves as a trigger for borate ester bonds protection-deprotection, whereby partial catechol primarily functions in non-sweating states and significantly activates during sweating. The VDBA hydrogel achieves a maximum adhesive strength of 13.45 kPa on skin at non-sweat, however, the maximum bonding strength increases to 24.0 kPa when sweating. The resultant VDBA hydrogel exhibits integration of exceptional mechanical properties and anti-freezing properties. Also, desirable conductivity appears in the hydrogel, allowing outputting accurate and repeatable signals for body motion sensing in various scenarios. Furthermore, VDBA hydrogel is demonstrated for use as a sports training times counter, which can achieve sensitive statistics for stretching and bending movements. This work provides a great hydrogel candidate for various motion sensor applications, particularly beneficial for people with sweaty skin and athletes.

A Universal Strategy for Constructing Hydrogel Assemblies Enabled by PAA Hydrogel Adhesive.

Hydrogel is a significant type of building block for constructing macroscopic assemblies, the construction of which usually entails the incorporation of supramolecular groups. However, supramolecular group recognition is specific and only suitable for assembling two particular modified hydrogels, but not a versatile strategy. Herein, a universal strategy without modification process is proposed using polyacrylic acid (PAA) hydrogel as the adhesive layer to assemble different kinds of hydrogels. Furthermore, hydrogel assemblies with various shapes and multi-stimuli responsiveness are constructed by assembling different stimuli-responsive hydrogels with PAA hydrogel. Therefore, hydrogel assemblies are able to complete bending motions upon applying corresponding stimuli. This strategy provides a universal approach for constructing hydrogel assemblies, and also shows the potential for developing soft robots with versatile functions.

Adhesive and conductive hydrogels based on poly(acrylic acid) composites for application as flexible biosensors

A PAA (polyacrylic acid)-based nanocomposite hydrogel (CASM) reinforced with sodium carboxymethyl cellulose (CMC-Na), organo-montmorillonite (OMMT), and sodium lignosulfonate (SLS) was prepared using free radical polymerization. In this work, CMC-Na was utilized to enhance the viscosity of the system, while the electrostatic interaction between CMC-Na and OMMT facilitated the uniform dispersion of OMMT within the matrix. Additionally, SLS aided in the dispersion of the components, reducing the interaction forces between particles in the hydrogel, thereby improving its flexibility and extensibility. The results demonstrated that the synergistic effects of CMC-Na, OMMT, and SLS led to a hydrogel with a tensile strength of up to 74.5 KPa, a tensile strain exceeding 3600 %, and certain shape memory properties. Furthermore, the incorporation of SLS, which provides phenolic hydroxyl and sulfonic groups, significantly enhanced the adhesive properties of the hydrogel, achieving a peel strength of up to 1200 N/m on aluminum. The sulfonic groups also facilitated ion transport, resulting in excellent electrical conductivity (9.82 mS/cm) and strain sensitivity (GF=4.36). This approach of improving hydrogel properties through the incorporation of inorganic particles and cross-linked structures offers a novel strategy for the multifunctional modification of hydrogels.

An Octopus-Inspired Stimulus-Responsive Structural Color Hydrogel for Uterus Cervical Canal Stent.

Soft-bodied aquatic organisms have exhibited remarkable capabilities in navigating and moving within liquid environments serving as a profound inspiration for the development of bionic robots with intricate movements. Traditional rigid components are being replaced by stimulus-responsive soft materials such as hydrogels and shape memory polymers, leading to the creation of dynamically responsive soft robots. In this study, the development of a bionic robot inspired by the shape of an octopus and the adsorptive properties of its tentacles, specifically tailored for targeted stimulation and pH sensing in the cervix, are presented. This approach involves the design of a soft, water-based Janus adhesive hydrogel patch that adheres to specific parts of the cervix and responds to pH changes through external stimuli. The hydrogel patch incorporates inverse opal microstructures mimicking the legs of an octopus, to facilitate efficient and stable locomotion, unidirectional transport of biofluids, and pH-responsive behavior. This miniature bionic robot showcases controlled adhesion and precise unidirectional fluid transport highlighting its potential for targeted stimulus response and pH sensing in the uterine cervical tract. This breakthrough opens new avenues for medical applications within the expanding field of soft-bodied robotics.

Green synthesis-inspired antibacterial, antioxidant and adhesive hydrogels with ultra-fast gelation and hemostasis for promoting infected skin wound healing

Bacterial infections are a serious threat to wound healing and skin regeneration. In recent years, photothermal therapy (PTT) has become one of the most promising tools in the treatment of infectious diseases. However, wound dressings with photo-responsive properties are currently still limited by the difficulties of biosafety and thermal stability brought by the introduction of photosensitizers or photothermal agents. Therefore, how to improve the therapeutic efficiency and biosafety from material design is still a major challenge at present. In this study, the carboxymethyl chitosan (CMCS) and protocatechuic aldehyde (PA) hydrogels based on horseradish peroxidase (HRP) and hydrogen peroxide (H2O2) enzymatic catalysis was developed. Therein, HRP and H2O2 catalyzed cross-linking while polymerizing PA, which not only endowed the hydrogels with photothermal responsiveness but also with good biosafety through this enzyme-catalyzed green approach. Meanwhile, the hydrogels possessed highly efficient bacteriostatic ability with the assistance of near infrared (NIR). Moreover, the ultra-rapid gelation, strong tissue adhesion, high swelling ability, good antioxidant property and hemostatic property of the CMCS-PA hydrogels based on HRP/H2O2 enzymatic catalysis were suitable for the treatment of skin wounds. Meanwhile, NIR-assistant CMCS-PA hydrogels based on HRP/H2O2 enzymatic catalysis reduced inflammation, decreased bacterial infection, and promoted collagen deposition and angiogenesis, which showed remarkable therapeutic effects in a skin wound infection model. All results indicate that this green approach to introduce photothermal property by HRP-catalyzed PA polymerization endows the hydrogels with efficient photothermal conversion efficiency, suggesting that they are promising to provide new options for replacing photothermal agents and photosensitizers. Statement of significanceIn recent years, wound dressings with photo-responsive properties are currently still limited by the difficulties of biosafety and thermal stability brought by the introduction of agent photosensitizers or photothermal agents. In this study, the carboxymethyl chitosan and protocatechuic aldehyde hydrogels based on horseradish peroxidase and hydrogen peroxide enzymatic catalysis was developed. The photothermal properties of hydrogels were transformed from absent to present just by horseradish peroxidase-catalyzed protocatechuic aldehyde polymerization in a green approach. Meanwhile, the hydrogels possessed highly efficient bacteriostatic ability with the assistance of near infrared. The green approach of introducing photothermal properties from material design solves the biosafety challenge. Therefore, this study is expected to provide new options for alternative photothermal agents and photosensitizers.

Strong and Thermo-Switchable Gel Adhesion Based on UCST-Type Phase Transition in Deep Eutectic Solvent.

It remains a great challenge to achieve strong and reversible hydrogel adhesion. Hydrogel adhesives also suffer from poor environmental stability due to dehydration. To overcome these problems, here reversible adhesive gels are designed using a new switching mechanism and new solvent. For the first time, the study observes UCST (upper critical solution temperature)-type thermosensitive behaviors of poly(benzyl acrylate) (PBnA) polymer and gel in menthol:thymol deep eutectic solvents (DESs). The temperature-induced phase transition allows adjusting cohesive force, and hence adhesion strength of PBnA gels by temperature. To further improve the mechanical and adhesion properties, a peptide crosslinker is used to allow energy dissipation when deforming. The resulting eutectogel exhibits thermal reversible adhesion with a high switching ratio of 14.0. The adhesion strength at attachment state reaches 0.627MPa, which is much higher than most reversible adhesive hydrogels reported before. The low vapor pressure of DES endows the gel excellent environmental stability. More importantly, the gel can be repeatedly switched between attachment and detachment states. The strong and reversible gel adhesive is successfully used to design soft gripper for the transport of heavy cargos and climbing robot capable of moving on vertical and inverted surface in a manner similar to gecko.

Polyphenol-mediated hyaluronic acid/tannic acid hydrogel with short gelation time and high adhesion strength for accelerating wound healing

Wound healing is a complex process involving a complicated interplay between numerous cell types and vascular systems. Hyaluronic acid (HA)-based hydrogel facilitates wound healing, and is involved in all processes. However, slow gelation speed and weak adhesion strength limit its ability to form a stable physical barrier quickly. Herein, we propose a HA-based composite hydrogel as the wound dressing based on oxidative coupling reaction. Tannic acid and dopamine-coated carbon particles (DCPs) containing abundant phenolic hydroxyl groups are incorporated into the HA-based hydrogel for increasing the number of crosslinking sites of oxidative coupling of the hydrogel and enhancing adhesion through the formation of covalent bonds and hydrogen bonds between hydrogel and wound sites. The composite hydrogel exhibits short gelation time (<6 s) and high adhesion strength (>8.1 kPa), which are superior to the references and commercial products of its kind. The in vitro experiments demonstrate that the hydrogel has low hemolytic reaction, negligible cytotoxicity, and the ability to promote fibroblast proliferation and migration. The in vivo full-thickness skin defect model experiments demonstrate that the hydrogel can accelerate wound healing under mild photothermal stimulation of DCPs by reducing inflammation, relieving tissue hypoxia, and promoting angiogenesis and epithelialization.

Wet tissue adhesive polymeric powder hydrogels for skeletal muscle regeneration

Volumetric muscle loss (VML) frequently results from traumatic incidents and can lead to severe functional disabilities. Hydrogels have been widely employed for VML tissue regeneration, which are unfortunately ineffective because of the lack of intimate contact with injured tissue for structural and mechanical support. Adhesive hydrogels allow for strong tissue connections for wound closure. Nevertheless, conventional adhesive hydrogels exhibit poor tissue adhesion in moist, bleeding wounds due to the hydration layer at the tissue–hydrogel interfaces, resulting in insufficient performance. In this study, we developed a novel, biocompatible, wet tissue adhesive powder hydrogel consisting of dextran-aldehyde (dex-ald) and gelatin for the regeneration of VML. This powder absorbs the interfacial tissue fluid and buffer solution on the tissue, spontaneously forms a hydrogel, and strongly adheres to the tissue via various molecular interactions, including the Schiff base reaction. In particular, the powder composition with a 1:4 ratio of dex-ald to gelatin exhibited optimal characteristics with an appropriate gelation time (258 s), strong tissue adhesion (14.5 kPa), and stability. Dex-ald/gelatin powder hydrogels presented strong adhesion to various organs and excellent hemostasis compared to other wet hydrogels and fibrin glue. A mouse VML injury model revealed that the dex-ald/gelatin powder hydrogel significantly improved muscle regeneration, reduced fibrosis, enhanced vascularization, and decreased inflammation. Consequently, our wet-adhesive powder hydrogel can serve as an effective platform for repairing various tissues, including the heart, muscle, and nerve tissues.

High tough, self‐adhesive, conductive double network hydrogel for flexible strain sensors

AbstractThe application of adhesive conductive hydrogel materials in flexible sensors has been extensively studied. However, existing adhesive hydrogel sensor materials have problems such as poor adhesion, low conductivity, and difficulty in balancing mechanical and adhesive properties, which limit their practical applications. In this study, we propose a simple and economical method to fabricate double‐network hydrogels for flexible strain sensors by dissolving acrylamide (AM), chitosan (CS), polyethylene glycol (PEG) and gelatin (Gel) in a mixed solvent of deionized water and a food‐grade phosphate. The prepared AM/CS/PEG/Gel (ACPG) hydrogel exhibits excellent toughness (maximum stress of 154 kPa, maximum elongation of 2256%), self‐adhesiveness (maximum adhesion strength to wood of 17.2 kPa), and high conductivity (2.33 S/m). Compared with similar adhesive hydrogels, the conductivity of ACPG hydrogel is significantly improved. Therefore, ACPG hydrogel can be used as an ideal material for flexible sensors, and has broad application potential in wearable devices and human‐computer interaction.

Multi-dynamic-bond cross-linked antibacterial and adhesive hydrogel based on boronated chitosan derivative and loaded with peptides from Periplaneta americana with on-demand removability

The design and development of a bio-adhesive hydrogel with on-demand removability and excellent antibacterial activities are meaningful to achieve high wound closure effectiveness and post-wound-closure care, which is desirable in clinical applications. In this work, a series of adhesive antioxidant antibacterial hydrogels containing peptides from Periplaneta americana (PAP) were prepared through multi-dynamic-bond cross-linking among 3,4-dihydroxybenzaldehyde (DBA) containing catechol and aldehyde groups and chitosan grafted with 3-carboxy-4-fluorophenylboronic acid (CS-FPBA) to enable the effective adhesion of skin tissues and prevention of bacterial infection of wound. PAP was derived from alcohol-extracted residues generated during the pharmaceutical process, aiming to minimize resource wastage and achieve the high-value development of such a medicinal insect. The hydrogel was prepared by freezing-thawing with no toxic crosslinkers. The multi-dynamic-bond cross-linking of dynamic borate ester bonds and dynamic Schiff base bonds can achieve reversible breakage and re-formation and the adhesive strength of CS-FPBA-DBA-P-gel treated with a 20 % glucose solution dramatically decreased from 3.79 kPa to 0.35 kPa within 10 s. Additionally, the newly developed hydrogel presents ideal biocompatibility, hemostasis and antibacterial activity against Staphylococcus aureus and Escherichia coli compared to commercial chitosan gel (approximately 50 % higher inhibition rate), demonstrating its great potential in dealing with infected full-thickness skin wounds.

Carbene-mediated gelatin and hyaluronic acid hydrogel paints with ultra adhesive ability for arthroscopic cartilage repair

In articular cartilage defect, particularly in arthroscopy, regenerative hydrogels are urgently needed. It should be able to firmly adhere to the cartilage tissue and maintain sufficient mechanical strength to withstand approximately 10 kPa of arthroscopic hydraulic flushing. In this study, we report a carbene-mediated ultra adhesive hybrid hydrogel paints for arthroscopic cartilage repair, which combined the photo initiation of double crosslinking system with the addition of diatomite, as a further reinforcing agent and biological inorganic substances. The double network consisting of ultraviolet initiated polymerization of hyaluronic acid methacrylate (HAMA) and carbene insertion chemistry of diazirine-grafted gelatin (GelDA) formed an ultra-strong adhesive hydrogel paint (H2G5DE). Diatomite helped the H2G5DE hydrogel paint firmly adhere to the cartilage defect, withstanding nearly 100 kPa of hydraulic pressure, almost 10 times that in clinical arthroscopy. Furthermore, the H2G5DE hydrogel supported cell growth, proliferation, and migration, thus successfully repairing cartilage defects. Overall, this study demonstrates a proof-of-concept of ultra-adhesive polysaccharide hydrogel paints, which can firmly adhere to the articular cartilage defects, can resist continuous hydraulic pressure, can promote effective cartilage regeneration, and is very suitable for minimally invasive arthroscopy.

Enhancing myocardial infarction treatment through bionic hydrogel-mediated spatial combination therapy via mtDNA-STING crosstalk modulation

Myocardial infarction (MI)-induced impaired cardiomyocyte (CM) mitochondrial function and microenvironmental inflammatory cascades severely accelerate the progression of heart failure for compromised myocardial repair. Modulation of the crosstalk between CM mitochondrial DNA (mtDNA) and STING has been recently identified as a robust strategy in enhancing MI treatment, but remains seldom explored. To develop a novel approach that can address persistent myocardial injury using this crosstalk, we report herein construction of a biomimetic hydrogel system, Rb1/PDA-hydrogel comprised of ginsenoside Rb1/polydopamine nanoparticles (Rb1/PDA NPs)-loaded carboxylated chitosan, 4-arm-PEG-phenylboronic acid (4-arm-PEG-PBA), and 4-arm-PEG-dopamine (4-arm-PEG-DA) crosslinked networks. An optimized hydrogel formulation presents not only desired adhesion properties to the surface of the myocardium, but also adaptability for deep myocardial injection, resulting in ROS scavenging, CM mitochondrial function protection, M1 macrophage polarization inhibition through the STING pathway, and angiogenesis promotion via an internal-external spatial combination. The enhanced therapeutic efficiency is supported by the histological analysis of the infarcted area, which shows that the fibrotic area of the MI rats decreases from 58.4% to 5.5%, the thickness of the left ventricular wall increases by 1-fold, and almost complete recovery of cardiac function after 28 days of treatment. Overall, this study reported the first use of a strong adhesive and injectable hydrogel with mtDNA and STING signaling characteristics for enhanced MI treatment via an internal-external spatial combination strategy.

The future path to sutureless surgery: Self–adhesive tough hydrogel

The future path to sutureless surgery: Self–adhesive tough hydrogel

On the design of lignin reinforced acrylic acid/hyaluronic acid adhesive hydrogels with conductive PEDOT:HA nanoparticles

Hydrogels are of great importance in biomedical engineering. They possess the ability to mimic bodily soft tissues, and this allows exciting possibilities for applications such as tissue engineering, drug delivery and wound healing, however much work remains on stability and mechanical robustness to allow for translation to clinical applications. The work herein describes the synthesis and analysis of a biocompatible, versatile hydrogel that has tailorable swelling, high stability when swollen and thermal stability. The synthesis methods used produce a hydrogel with high elasticity, good mechanical properties and rapid crosslinking whilst displaying biocompatibility, adhesion, and conductivity. It has been shown that cell viability in the samples is above 80 % in all cases, a Young's Modulus of up to 85 kPa and high swelling degrees were achieved. These materials show potential for use in numerous applications such as adhesive sensors, skin grafts and drug delivery systems.

Chain-like One-Dimensional Assembly of Mesoporous Silica Nanoparticles: An Approach To Improve Hydrogel Adhesion.

Mesoporous silica nanoparticles (MSNPs) are well known for their adhesive properties with hydrogels and living tissues. However, achieving direct contact between the silica nanoparticle surface and the adherend necessitates the removal of capping agents, which can lead to severe aggregation when exposed to wet surfaces. This aggregation is ineffective for simultaneously bridging the two adherends, resulting in a reduced adhesive strength. In this study, we designed and synthesized mesoporous silica nanochains (MSNCs) to enhance the interactions with hydrogels by promoting the formation of coarser structures with increased nanopore exposure. Chain-like one-dimensional assemblies in the MSNCs were generated by depleting the capping ligand, cetyltrimethylammonium bromide, from the surface of the MSNPs. To quantify the porous areas of the MSNCs, we analyzed scanning electron microscopy (SEM) images using an in-house SEM image analysis algorithm. Additionally, we conducted a comparative assessment of the adhesion energies of MSNCs and MSNPs on a poly(dimethylacrylamide) hydrogel using a universal testing machine. The MSNCs exhibited a maximum adhesion energy of 13.7 ± 0.7 J/m2 at 3 wt %, surpassing that of MSNPs (10.9 ± 0.3 J/m2) at 2 wt %. Moreover, the unique stacking structure of the MSNCs enabled them to maintain an adhesion energy of 13.4 ± 1.0 J/m2 at a high concentration of 9 wt %, whereas the adhesion energy of MSNPs decreased to 8.2 ± 0.4 J/m2. This underscores their potential as superior hydrogel adhesives in challenging wet tissue-like environments.

Ink-based textile electrodes for wearable functional electrical stimulation: A proof-of-concept study to evaluate comfort and efficacy.

Functional Electrical Stimulation (FES) represents a promising technique for promoting functional recovery in individuals with neuromuscular diseases. Traditionally, current pulses are delivered through self-adhesive hydrogel Ag/AgCl electrodes, which allow a good contact with the skin, are easy-to-use and have a moderate cost. However, skin adherence decreases after a few uses and skin irritations can originate. Recently, textile electrodes have become an attractive alternative as they assure increased durability, easy integration into clothes and can be conveniently cleaned, improving the wearability of FES. However, as various manufacture processes were attempted, their clear validation is lacking. This proof-of-concept study proposes a novel set of ink-based printed textile electrodes and compares them to adhesive hydrogel electrodes in terms of impedance, stimulation performance and perceived comfort. The skin-electrode impedance was evaluated for both types of electrodes under different conditions. These electrodes were then used to deliver FES to the Rectus Femoris of 14 healthy subjects to induce its contraction in both isometric and dynamic conditions. This allowed to compare the two types of electrodes in terms of sensory, motor, maximum and pain thresholds, FES-induced range of motion during dynamic tests, FES-induced torque during isometric tests and perceived stimulation comfort. No statistically significant differences were found both in terms of stimulation performance (Wilcoxon test) and comfort (Generalized Linear Mixed Model). The results showed that the proposed ink-based printed textile electrodes can be effectively used as alternative to hydrogel ones. Further experiments are needed to evaluate their durability and their response to sterilizability and stretching tests.

Hydrogel network of polyvinyl alcohol (PVA), pyrogallol (PG) and Fe(III) for building superhydrophilic PVDF membrane

High hydrophobicity of polyvinylidene fluoride (PVDF) membrane surface results in adsorption of oil droplets and membrane fouling. A hydrogel coating with crosslinking network of polyvinyl alcohol (PVA), pyrogallol (PG) and Fe(III) based on PVDF membrane was proposed. Hydrogen bonds between PVA and PG in water were regulated by ethanol to form a uniform hydrophilic hydrogel coating on PVDF membrane. Chelation between PG and Fe3+ significantly enhanced hydrogel adhesion. The surface energy of the developed PVDF-PVA/PG-Fe3+ membrane was 39.96 mJ·m−2, 2.71 times that of the pristine PVDF membrane, while its adhesion to oil is close to 0 μN. The permeate flux reached 1341 L·m−2· h−1 at 0.1 bar for separating isooctane-in-water emulsions with good separation efficiency (>99 %) and cycling stability. The developed membrane could also effectively separate petroleum ether-in-water and dodecane-in-water emulsions.

Bionic double-crosslinked hydrogel of poly (γ-glutamic acid)/poly (N-(2-hydroxyethyl) acrylamide) with ultrafast gelling process and ultrahigh burst pressure for emergency rescue

Injectable adhesive hydrogels combining rapid gelling with robust adhesion to wet tissues are highly required for fast hemostasis in surgical and major trauma scenarios. Inspired by the cross-linking mechanism of mussel adhesion proteins, we developed a bionic double-crosslinked (BDC) hydrogel of poly (γ-glutamic acid) (PGA)/poly (N-(2-hydroxyethyl) acrylamide) (PHEA) fabricated through a combination of photo-initiated radical polymerization and hydrogen bonding cross-linking. The BDC hydrogel exhibited an ultrafast gelling process within 1 s. Its maximum adhesion strength to wet porcine skin reached 254.5 kPa (9 times higher than that of cyanoacrylate (CA) glue) and could withstand an ultrahigh burst pressure of 626.4 mmHg (24 times higher than that of CA glue). Notably, the BDC hydrogel could stop bleeding within 10 s from a rat liver incision 10 mm long and 5 mm deep. The wound treated with the BDC hydrogel healed faster than the control groups, underlining the potential for emergency rescue and wound care scenarios.

Tannic acid strengthen adhesion of poly(AAm-co-GG) hydrogels for multiple solid surfaces repairing

This study aims to develop bio-compatible mechanically robust, adhesive hydrogels using acrylamide and gellan gum. Tannic acid (TA) and N, N-methylene bisacrylamide (MBA) were used as physical and chemical crosslinkers respectively. Fourier transform infrared (FT-IR) and scanning electron microscopy (SEM) analysis verified the successful synthesis of hydrogels through free radical addition polymerization. The rheological tests, such as frequency sweep, creep recovery, and amplitude sweep were performed to evaluate the effect of TA on the adhesive behavior and viscoelastic properties of hydrogels. Results highlighted the pivotal role of polymer chain interactions in regulating the adhesive behavior. The tannic acid concentration was varied to assess the adhesive performance, higher tannic acid concentration resulted in improved adherence. The adhesion strength order was received as 33.6 > 18 > 7.56 > 6.7 > 6.23 kPa. The prepared adhesive hydrogels performed exceptionally well on wood, cloth, rubber, glass, and ceramics-like materials. Furthermore, the hydrogels were practically found efficient at low as well as at high temperatures. The low price, high efficiency, easy to synthesize, and bio-friendly. etc. characteristics can make these hydrogels to be applied convincingly as adhesives in the future.

Mussel-inspired tissue adhesive composite hydrogel with photothermal and antioxidant properties prepared from pectin for burn wound healing

Biodegradable self-healing hydrogels with antibacterial property attracted growing attentions in biomedication as wound dressings since they can prevent bacterial infection and promote wound healing process. In this research, a biodegradable self-healing hydrogel with ROS scavenging performance and enhanced tissue adhesion was fabricated from dopamine grafted oxidized pectin (OPD) and naphthoate hydrazide terminated PEO (PEO NH). At the same time, Fe3+ ions were incorporated to endow the hydrogel with near-infrared (NIR) triggered photothermal property to obtain antibacterial activity. The composite hydrogel showed good hemostasis performance based on mussel inspired tissue adhesion with biocompatibility well preserved. As expected, the composition of FeCl3 improved conductivity and endowed photothermal property to the hydrogel. The in vivo wound repairing experiment revealed the 808 nm NIR light triggered photothermal behavior of the hydrogel reduced the inflammation response and promoted wound repairing rate. As a result, this composite FeCl3/hydrogel shows great potential to be an excellent wound dressing for the treatment of infection prong wounds with NIR triggers.