Multiple Crosslinking Research Articles

Oxidized sodium alginate cross-linked calcium alginate/antarctic krill protein composite fiber for improving strength and water resistance

Oxidation Sodium alginate is a naturally derived cross-linking agent. It has the advantages of high biocompatibility, no precipitation, and low toxicity that small-molecule aldehydes do not possess. Herein, we employed sodium periodate for the oxidation of sodium alginate (SA) to produce oxidized sodium alginate (OSA) aldehyde-based crosslinker, which was used to crosslink calcium alginate (CA)/Antarctic krill protein (AKP) composite fibers to obtain OSA-co-CA/AKP composite fibers with multiple crosslinking networks. FT-IR was used to analyze the multiple cross-linked network construction and the hydrogen bonding mechanisms. The composite fibers' crystallinity, morphological structure, and thermal and mechanical properties were analyzed by XRD, SEM, DSC, TGA, and a single fiber strength meter, respectively. The results showed that the composite fibers possessed a multi-network structure of covalent bonding-ionic complexation-hydrogen bonding. And the inclusion of OSA enhanced the composite fibers' thermal stability, crystallinity, and mechanical properties. When the OSA was 1.64 wt%, the fracture strength and salt resistance increased by 16.58 % and 44.2 %, respectively. Cell Counting Kit-8 cytotoxicity test also verified its good biocompatibility and confirmed its potential as a biomedical material.

Enhancing cartilage repair with optimized supramolecular hydrogel-based scaffold and pulsed electromagnetic field.

Functional tissue engineering strategies provide innovative approach for the repair and regeneration of damaged cartilage. Hydrogel is widely used because it could provide rapid defect filling and proper structure support, and is biocompatible for cell aggregation and matrix deposition. Efforts have been made to seek suitable scaffolds for cartilage tissue engineering. Here Alg-DA/Ac-β-CD/gelatin hydrogel was designed with the features of physical and chemical multiple crosslinking and self-healing properties. Gelation time, swelling ratio, biodegradability and biocompatibility of the hydrogels were systematically characterized, and the injectable self-healing adhesive hydrogel were demonstrated to exhibit ideal properties for cartilage repair. Furthermore, the new hydrogel design introduces a pre-gel state before photo-crosslinking, where increased viscosity and decreased fluidity allow the gel to remain in a semi-solid condition. This granted multiple administration routes to the hydrogels, which brings hydrogels the ability to adapt to complex clinical situations. Pulsed electromagnetic fields (PEMF) have been recognized as a promising solution to various health problems owing to their noninvasive properties and therapeutic potentials. PEMF treatment offers a better clinical outcome with fewer, if any, side effects, and wildly used in musculoskeletal tissue repair. Thereby we propose PEMF as an effective biophysical stimulation to be 4th key element in cartilage tissue engineering. In this study, the as-prepared Alg-DA/Ac-β-CD/gelatin hydrogels were utilized in the rat osteochondral defect model, and the potential application of PEMF in cartilage tissue engineering were investigated. PEMF treatment were proven to enhance the quality of engineered chondrogenic constructs in vitro, and facilitate chondrogenesis and cartilage repair in vivo. All of the results suggested that with the injectable self-healing adhesive hydrogel and PEMF treatment, this newly proposed tissue engineering strategy revealed superior clinical potential for cartilage defect treatment.

β-heavy-spectrin stabilizes the constricting contractile ring during cytokinesis.

Cytokinesis requires the constriction of an actomyosin-based contractile ring and involves multiple F-actin crosslinkers. We show that partial depletion of the C. elegans cytokinetic formin generates contractile rings with low F-actin levels that constrict but are structurally fragile, and we use this background to investigate the roles of the crosslinkers plastin/PLST-1 and β-heavy-spectrin/SMA-1 during ring constriction. We show that the removal of PLST-1 or SMA-1 has opposite effects on the structural integrity of fragile rings. PLST-1 loss reduces cortical tension that resists ring constriction and makes fragile rings less prone to ruptures and regressions, whereas SMA-1 loss exacerbates structural defects, leading to frequent ruptures and cytokinesis failure. Fragile rings without SMA-1 or containing a shorter SMA-1, repeatedly rupture at the same site, and SMA-1::GFP accumulates at repair sites in fragile rings and in rings cut by laser microsurgery. These results establish that β-heavy-spectrin stabilizes the constricting ring and reveals the importance of β-heavy-spectrin size for network connectivity at low F-actin density.

An Efficient Cross-Linked Phosphorus-Free Flame Retardant for Epoxy Resins.

Epoxy resins (EPs) have been widely used due to their great physical and chemical properties, but their poor flame retardancy limits their further application. In this work, we synthesized a flame retardant containing nitrile groups and a double bond to improve the flame retardancy of EPs. In this way, multiple cross-linking reactions can occur in the EPs to confer better flame retardancy by a simple heat treatment. The UL-94 vertical combustion test, CCT, and limiting oxygen index (LOI) test were used to characterize the flame retardant properties of the cross-linked flame retardant; the results show that with the 10 wt % addition of cross-linked flame retardant, the thermosets can pass the UL-94 V-0 rating. Meanwhile, the contents reached 20 wt %, and the peak heat release rate decreased 40% compared with neat EP.

Nanofibrils of food-grade proteins: Formation mechanism, delivery systems, and application evaluation.

Due to the high aspect ratio, appealing mechanical characteristics, and various adjustable functional groups on the surface proteins, food-grade protein nanofibrils have attracted great research interest in the field of food science. Fibrillation, known as a process of peptide self-assembly, is recognized as a common attribute for food-grade proteins. Converting food-grade proteins into nanofibrils is a promising strategy to broaden their functionality and applications, such as improvement of the properties of gelling and emulsifying, especially for constructing various delivery systems for bioactive compounds. Protein source and processing conditions have a great impact on the size, structure, and morphology of nanofibrils, resulting in extreme differences in functionality. With this feature, it is possible to engineer nanofibrils into four different delivery systems, including gels, microcapsules, emulsions, and complexes. Construction of nanofibril-based gels via multiple cross-linking methods can endow gels with special network structures to efficiently capture bioactive compounds and extra mechanical behavior. The adsorption behavior of nanofibrils at the interface is highly complex due to the influence of several intrinsic factors, which makes it challenging to form stabilized nanofibril-based emulsion systems. Based on electrostatic interactions, microcapsules and complexes prepared using nanofibrils and polysaccharides have combined functional properties, resulting in adjustable release behavior and higher encapsulation efficiency. The bioactive compounds delivery system based on nanofibrils is a potential solution to enhance their absorption in the gastrointestinal tract, improve their bioavailability, and deliver them to target organs. Although food-grade protein nanofibrils show unknown toxicity to humans, further research can contribute to broadening the application of nanofibrils in delivery systems.

Causative or associative: A critical review of the role of advanced glycation end-products in bone fragility.

The accumulation of advanced glycation end-products (AGEs) in the organic matrix of bone with aging and chronic disease such as diabetes is thought to increase fracture risk independently of bone mass. However, to date, there has not been a clinical trial to determine whether inhibiting the accumulation of AGEs is effective in preventing low-energy, fragility fractures. Moreover, unlike with cardiovascular or kidney disease, there are also no pre-clinical studies demonstrating that AGE inhibitors or breakers can prevent the age- or diabetes-related decrease in the ability of bone to resist fracture. In this review, we critically examine the case for a long-standing hypothesis that AGE accumulation in bone tissue degrades the toughening mechanisms by which bone resists fracture. Prior research into the role of AGEs in bone has primarily measured pentosidine, an AGE crosslink, or bulk fluorescence of hydrolysates of bone. While significant correlations exist between these measurements and mechanical properties of bone, multiple AGEs are both non-fluorescent and non-crosslinking. Since clinical studies are equivocal on whether circulating pentosidine is an indicator of elevated fracture risk, there needs to be a more complete understanding of the different types of AGEs including non-crosslinking adducts and multiple non-enzymatic crosslinks in bone extracellular matrix and their specific contributions to hindering fracture resistance (biophysical and biological). By doing so, effective strategies to target AGE accumulation in bone with minimal side effects could be investigated in pre-clinical and clinical studies that aim to prevent fragility fractures in conditions that bone mass is not the underlying culprit.

In Situ Spontaneous Fabrication of Tough and Stretchable Polyurethane-Polyethyleneimine Hydrogels Selectively Triggered by CO2.

CO2 -triggered in situ hydrogels is developed from waterborne poly(ε-caprolactone)-based polyurethane (PU) dispersion and aqueous polyethyleneimine (PEI) solution without any other chemicals and apparatus (e.g., UV light). In the approach, nontoxic CO2 in air is used as a selective trigger for the hydrogel formation. CO2 adsorption onto PEI results in the formation of ammonium cations in PEI and the subsequent multiple ionic crosslinking between PU and PEI chains. Besides the amount of CO2 in air, the rate of hydrogel formation can be controlled by NaHCO3 in the PU-PEI mixture, which serves as a CO2 supplier. The PU hydrogels exhibit tough and stretchable properties with high tensile strength (2.05 MPa) and elongation at break (438.24%), as well as biocompatibility and biodegradability. In addition, the PU hydrogels exhibit high adhesion strength on skin and injectability due to the in situ formation. It is believed that these PU hydrogels have the ideal features for various future applications, such as tissue adhesion barriers, wound dressing, artificial skin, and injectable fillers.

Application of Multiple Length Cross-linkers to the Characterization of Gaseous Protein Structure.

The speed, sensitivity, and tolerance of heterogeneity, as well as the kinetic trapping of solution-like states during electrospray, make native mass spectrometry an attractive method to study protein structure. Increases in the resolution of ion mobility measurements and in mass resolving power and range are leading to the increase of the information content of intact protein measurements and an expanded role of mass spectrometry in structural biology. Herein, a suite of different length noncovalent (sulfonate to positively charged side chain) cross-linkers was introduced via gas-phase ion/ion chemistry and used to determine distance restraints of kinetically trapped gas-phase structures of native-like cytochrome c ions. Electron capture dissociation allowed for the identification of cross-linked sites. Different length linkers resulted in distinct pairs of side chains being linked, supporting the ability of gas-phase cross-linking to be structurally specific. The gas-phase lengths of the cross-linkers were determined by conformational searches and density functional theory, allowing for the interpretation of the cross-links as distance restraints. These distance restraints were used to model gas-phase structures with molecular dynamics simulations, revealing a mixture of structures with similar overall shape/size but distinct features, thereby illustrating the kinetic trapping of multiple native-like solution structures in the gas phase.

Effect of Hardener Type on the Photochemical and Antifungal Performance of Epoxy and Oligophosphonate S-IPNs.

Due to their highly reactive character and multiple crosslinking capacity, epoxy resins are one of the worldwide market-dominating classes of thermosetting polymers and are present in a wide range of technical applications, including structural adhesives, coatings and polymer matrices for composite materials. Despite their excellent features, epoxy resins are known to be highly flammable and possess low thermal stability and a brittle character and crack easily under impact forces. An efficient approach towards eliminating such drawbacks resides in obtaining epoxy-based semi-interpenetrating polymer networks, which possess excellent control over the morphology. The article describes the comparative effect of three hardeners (aromatic, cycloaliphatic and aliphatic) in the presence of an oligophosphonate (–R–O–PO(C6H5)–O–) (2 wt.% phosphorus) on the photochemical, fire and antifungal performance of bisphenol A diglycidyl ether semi-interpenetrating polymer networks. The networks are designed as future potential outdoor protective coatings for different substrates. The fire resistance capacity of the networks was undertaken with microscale combustion calorimetry before and after photochemical aging. Structural changes during photoirradiation were monitored via color modification studies, Fourier-transform infrared spectroscopy, differential scanning calorimetry, morphological assessment through scanning electron microscopy and mass loss measurements in order to propose the action mode of the hardeners and the oligophosphonate on the material properties. Microbiological testing was also undertaken with the aid of three specific wood decaying fungi as a first substrate.

A supramolecular injectable hydrogel based on β-cyclodextrin-grafted alginate and pluronic-amine loaded with kartogenin for chondrogenic differentiation of mesenchymal stem cells

Owing to the similarity of hydrogels to cartilage extracellular matrix, they have been extensively utilized in the chondral lesions. Moreover, their tunable administration properties are desirable for reducing injuries in lesion sites. Generally, injectable hydrogels are mechanically weak, requiring some modifications for being used as a cell carrier in place of articular cartilage. In this study, a combination of β-cyclodextrin-grafted alginate (Alg-β-CD) and pluronic-amine with multiple physical crosslinking was used for the first time. Supramolecular interactions, including electrostatic forces, host-guest interaction, and hydrophobic interaction with increasing temperature maintain injectability of hydrogels while these interactions boost mechanical properties to the extent that shear modulus surpassed 40 kPa. Vacant β-CD cavities in conjunction with gel network were exploited for kartogenin (KGN) loading. All groups had gel time of less than one minute and gel temperature was 28 °C. No toxic effect of hydrogels on encapsulated cells was observed. While the optimum combination of polymers provided a sustainable release for KGN, it also extended the in vitro degradation time of hydrogels from six days to two weeks. KGN facilitated encapsulated mesenchymal stem cells differentiation towards chondrocytes. Taken together, the synthesized hydrogel proved to be a promising candidate for being utilized in cartilage regeneration.

High-temperature soybean meal adhesive based on disulfide bond rearrangement and multiple crosslinking: Water resistance and prepressing adhesion

The main aim of this work is to prepare a high-temperature soybean meal (HSM) wood adhesive with excellent water resistance and prepressing adhesion to satisfy the requirements of green wood-based composites. Different from traditional complex modification methods, a lignosulfonate (LS)-assisted thiol-grafted polyamide-epichlorohydrin (PAE-SH) reinforced HSM wood adhesive was developed via a simple and novel design. The reduced –SH groups were grafted onto polyamide-epichlorohydrin (PAE) to break the S–S in HSM proteins and prompt a disulfide bonds rearrangement between PAE-SH and protein. LS was then introduced into PAE-SH to induce multiple crosslinking interactions, including cation-π interactions and electrostatic interactions. The generation of the LS-assisted PAE-SH not only contributed to the formation of a stable multiple cross-linked adhesive system for strong cohesion, but also provided a suitable solid content of adhesives for the formation of mechanical nail in plywood veneers. The plywood bonded using the PAE-SH/LS-modified adhesive displayed a wet bonding strength of 1.41 MPa, which is 402.9% higher than that of the neat soybean meal adhesive. It was also showed a prepressing bonding strength of 548 kPa, which is more than twice of the pure HSM-based adhesive (245 kPa), greatly reducing the transportation difficulty of veneers before being hot-pressed. This study provides a novel strategy for preparing a water-resistant protein-based adhesives with great potential for industrial application.

Bioinspired phenol-amine chemistry for developing bioadhesives based on biomineralized cellulose nanocrystals

Inspired by the phenol-amine chemistry and biomineralization of insect cuticles, we developed a green and facile strategy for preparing a bio-adhesive with excellent adhesion properties, mildew resistance, and antibacterial activity. This biomimetic strategy incorporates functional catechol-modified ε-polylysine and vanillin via grafting and Schiff base reactions. The biomineralized cellulose nanocrystals were prepared using a cellulose nanocrystal bio-template by regulating the in-situ biomineralization of inorganic nanoparticles, thereby building an optimized organic–inorganic mineralization framework in the polymer. The bonding strength of composite adhesive was significantly improved by multiple cross-linking networks through sacrificial hydrogen bonds, electrostatic interactions, and dynamic covalent bonds. The adhesion strength of the composite adhesive reached 1.13 MPa, which was 151% higher than the pristine adhesive. As a result of the synergistic effect of the catechol component, cationic ε-polylysine, and aldehyde group, the bio-adhesive also exhibited favorable anti-mildew and anti-bacterial properties.

Metal-assisted multiple-crosslinked thin film composite hollow fiber membrane for highly efficient bioethanol purification

Polyamide (PA)-based thin film composite (TFC) membranes have been extensively applied in various membrane-based separations. However, research works for bioethanol purification are relatively limited due to insufficient hydrophilicity and chain packing density of the PA selective layer by conventional interfacial polymerization. In this work, a new TFC hollow fiber (HF) membrane is fabricated by metal-assisted multiple crosslinking strategy, that is, metal-coordinated crosslinking of the pristine PA layer and coordination complexation between metal ions and phytic acid (PhA) for advanced water/ethanol separation. By tuning coordination abilities of metal ions with PA and PhA and the cycle number of PhA/metal ion assembly, PA-based TFC HF membrane is perfected. Additionally, a joint experiment/simulation characterization is deployed to reveal the coordination abilities of various metal ions with the pristine PA and grafted PhA. Ultimately, the synergistic effect between PA layer and PhA-metal ion complexes (i.e., 1 + 1 > 2 effect) is embodied in the separation performance of water/ethanol separation. The resulting TFC-Fe3+-PhA membrane with the strongest PhA-metal ion coordination ability exhibits the best water/ethanol separation performance, i.e., the separation factor of 1703 (34 times higher than pristine PA TFC HF membrane) and total flux of 1705 g/m2 h. This metal-assisted multiple crosslinking strategy is therefore believed to shed important lights on the development of next-generation high-performance TFC membranes for bioethanol purification.

A facile strategy for high mechanical performance and recyclable EPDM rubber enabled by exchangeable ion crosslinking

Endowing rubber with excellent recycling ability is of great significance for energy conservation. It is still a huge challenge to obtain high-performance recyclable commercial rubber to satisfy practical applications. Herein, a facile strategy of incorporating exchangeable Zn2+-carboxyl crosslinks into commercial EPDM system was developed through reaction of zinc acetate and EPDM grafted maleic anhydride (EPDM-g-MAH) to obtain EPDM-g-MAZn. The constructed exchangeable crosslinking networks as sacrificial unit significantly enhanced mechanical properties of EPDM, much higher than EPDM cured by covalent bonds (tensile strength: 2.00 MPa and fracture toughness: 6.75 MJ/m3). The dynamic crosslinking was reversibly broken and reformed by hot pressing, endowing EPDM-g-MAZn with good recycling ability. The promising mechanical properties of EPDM-g-MAZn can be tailored by incorporation of carbon black (CB) or zinc dimethacrylate (ZDMA), and recycled EPDM-g-MAZn/CB exhibited good mechanical properties to meet industrial applications. Additionally, multiple crosslinking networks were constructed for EPDM-g-MAZn/ZDMA with fine dispersion of ZDMA due to Zn2+-carboxyl interactions. Such effective strategy exhibits a promising perspective in industrial applications of high-performance recyclable rubber field.

Healable, recyclable and mechanically robust elastomers with multiple dynamic cross-linking bonds

The cross-linked network structure bestows rubber with excellent mechanical properties, but it greatly limits the self-healing and reprocessing ability of rubber. Herein, to address the above problem, we propose a simple cross-linking strategy with the cross-linker consisting of triple dynamic covalent bonds to vulcanize epoxidized natural rubber (ENR). A dynamic covalent network remarkably enhanced the mechanical properties of ENR through the combination of dynamic covalent bonds in the cross-linked network. At the same time, abundant dynamic covalent bonds rearranged the network topology through reversible exchange. As a result, a novel self-healing ENR with high tensile strength (2.06 ± 0.12 MPa) has been successfully developed. The ENR exhibits a high (97 ± 3%) self-healing efficiency (after 30 h at 70 °C) without applying any external force. Furthermore, it can be recycled more than three times. This work could enlighten researchers in academia and industry to develop self-healing elastomers with mechanical strength and reprocessing ability. • A novel cross-linker containing triple dynamic covalent bonds was synthesized. • Triple dynamic covalent bonds is simultaneously introduced into the cross-linked network. • The covalent cross-linking driven by dynamic covalent bonds reinforce the mechanical properties of rubber. • Reversible interactions enable the self-healing ability and recyclability of rubber.

Manufacturing of self-standing multi-layered 3D-bioprinted alginate-hyaluronate constructs by controlling the cross-linking mechanisms for tissue engineering applications

Three-dimensional (3D) bioprinting of self-supporting stable tissue and organ structure is critically important in extrusion-based bioprinting system, especially for tissue engineering and regenerative medicine applications. However, the development of self-standing bioinks with desired crosslinking density, biocompatibility, tunable mechanical strength and other properties like self-healing, in situ gelation, drug or protein incorporation is still a challenge. In this study, we report a hydrogel bioink prepared from alginate (Alg) and hyaluronic acid (HA) crosslinked through multiple crosslinking mechanisms, i.e. acyl-hydrazone, hydrazide interactions and calcium ions. These Alg-HA gels were highly dynamic and shear-thinning with exceptional biocompatibility and tunable mechanical properties. The increased dynamic nature of the gels is mainly chemically attributed to the presence of acyl-hydrazone bonds formed between the amine groups of the acyl-hydrazide of alginate and the monoaldehyde of the HA. Among the different combinations of Alg-HA gel compositions prepared, the A5H5 (Alginate-acyl-hydrazide:HA-monoaldehyde, ratio 50:50) gel showed a gelation time of ∼60 s, viscosity of ∼400 Pa s (at zero shear rate), high stability in various pH solutions and increased degradation time (>50 days) than the other samples. The A5H5 gels showed high printability with increased post-printing stability as observed from the 3D printed structures (e.g. hollow tube (∼100 layers), porous cube (∼50 layers), star, heart-in, meniscus and lattice). The scanning electron microscopy analysis of the 3D constructs and hydrogels showed the interconnected pores (∼181 µm) and crosslinked networks. Further, the gels showed sustained release of 5-amino salicylic acid and bovine serum albumin. Also, the mechanical properties were tuned by secondary crosslinking via different calcium concentrations. In vitro assays confirmed the cytocompatibility of these gels, where the 3D bioprinted lattice and tubular (∼70 layers) constructs demonstrated high cell viability under fluorescence analysis. In in vivo studies, Alg-HA gel showed high biocompatibility (>90%) and increased angiogenesis (threefolds) and reduced macrophage infiltration (twofold decrease), demonstrating the promising potential of these hydrogels in 3D bioprinting applications for tissue engineering and regenerative medicine with tunable properties.

Super-strong and anti-tearing poly(vinyl alcohol)/graphene oxide nano-composite hydrogels fabricated by formation of multiple crosslinking bonding network structure

As load-bearing material in biomedical-applications as cartilage replacement, artificial meniscus and tendons, etc., poly(vinyl alcohol) (PVA)/graphene oxide (GO)-tannic acid (TA) nano-composite hydrogels with multiple-crosslinking network were fabricated by establishing freezing/thawing-annealing-swelling method. By TA anchoring, PVA molecules were grafted onto GO surface efficiently, and strong interfacial interaction led to exfoliation and uniform distribution of GO in matrix. By introducing annealing process, the crystallinity and crystallite size of PVA increased and introducing GO-TA led to more perfect and denser crystalline structure, while physical crosslinking network centered on GO-TA and hydrogen bond-abundant crystalline phase formed, resulting in increasing crosslinking density of hydrogel. By further swelling in CaCl2 aqueous solution, hydroxyl-Ca2+ coordination formed, and multiple-crosslinking network was constructed with high crosslinking density. The tensile strength and fracture toughness of composite hydrogel were remarkably improved, reaching 14.38 MPa/27.93 MJ/m3, approximately 11-/26-fold higher than those of neat PVA hydrogel, while tearing strength was significantly enhanced, attributed to high energy dissipation through unzipping multiple interactions.

Dendrobium officinale Enzyme Changing the Structure and Behaviors of Chitosan/γ-poly(glutamic acid) Hydrogel for Potential Skin Care.

Hydrogels have been widespreadly used in various fields. But weak toughness has limited their further applications. In this study, Dendrobium officinale enzyme (DOE) was explored to improve chitosan/γ-poly(glutamic acid) (CS/γ-PGA) hydrogel in the structure and properties. The results indicated that DOE with various sizes of ingredients can make multiple noncovalent crosslinks with the skeleton network of CS/γ-PGA, significantly changing the self-assembly of CS/γ-PGA/DOE hydrogel to form regular protuberance nanostructures, which exhibits stronger toughness and better behaviors for skin care. Particularly, 4% DOE enhanced the toughness of CS/γ-PGA/DOE hydrogel, increasing it by 116%. Meanwhile, water absorption, antioxygenation, antibacterial behavior and air permeability were increased by 39%, 97%, 27% and 52%.

An Extensively Adhesive Patch with Multiple Physical Interactions and Chemical Crosslinking as a Wound Dressing and Strain Sensor

An Extensively Adhesive Patch with Multiple Physical Interactions and Chemical Crosslinking as a Wound Dressing and Strain Sensor

Carboxymethyl chitosan-based multifunctional hydrogels incorporated with photothermal therapy against drug-resistant bacterial wound infection

Wound infection especially that induced by drug resistant bacteria has been considered an increasing medical crisis. Herein a biocompatible wound dressing is conveniently constructed by incorporating (Sr0.6Bi0.305)2Bi2O7 (denoted as SBO) with excellent photothermal performance into a facile antibacterial hydrogel (gel) obtained from multiple physical crosslinks among Ag+, carboxymethyl chitosan and polyacrylic acid. The prepared SBO gel features excellent bactericidal activities, hemostasis, adequate mechanical properties, adhesiveness and adsorption capacities to bacterial cells and toxin. The gel can disperse SBO homogeneously in the network and SBO effectively convert visible light energy into localized heat for synergistic sterilization. In vitro assays confirm the potent broad-spectrum bactericidal activities of SBO gel to some common pathogens and drug resistant strains such as MRSA and CAPA. Mice model of MRSA-induced wound infections verified the practical efficacy of SBO gel in combating bacterial infections and accelerating wound healing. Moreover, this is the first report of SBO as a photothermal agent applied in anti-infection treatment. All of these results highlight the potential application of SBO gel in drug-resistant bacteria associated wound management.