Hydrogel Fibers Research Articles

Recent Development of Fibrous Hydrogels: Properties, Applications and Perspectives.

Fibrous hydrogels (FGs), characterized by a 3D network structure made from prefabricated fibers, fibrils and polymeric materials, have emerged as significant materials in numerous fields. However, the challenge of balancing mechanical properties and functions hinders their further development. This article reviews the main advantages of FGs, including enhanced mechanical properties, high conductivity, high antimicrobial and anti-inflammatory properties, stimulus responsiveness, and an extracellular matrix (ECM)-like structure. It also discusses the influence of assembly methods, such as fiber cross-linking, interfacial treatments of fibers with hydrogel matrices, and supramolecular assembly, on the diverse functionalities of FGs. Furthermore, the mechanisms for improving the performance of the above five aspects are discussed, such as creating ion carrier channels for conductivity, in situ gelation of drugs to enhance antibacterial and anti-inflammatory properties, and entanglement and hydrophobic interactions between fibers, resulting in ECM-like structured FGs. In addition, this review addresses the application of FGs in sensors, dressings, and tissue scaffolds based on the synergistic effects of optimizing the performance. Finally, challenges and future applications of FGs are discussed, providing a theoretical foundation and new insights for the design and application of cutting-edge FGs.

Extracellular matrix mimetic supramolecular hydrogels reinforced with covalent crosslinked mesoporous silica nanoparticles.

The extracellular matrix (ECM) is a dynamic environment that is primarily built up from fibrous proteins (e.g., elastins, fibronectins, collagens, and laminins) and plays a vital role in tissue regeneration processes. Therefore, the development of supramolecular hydrogels that can mimic the ECM's dynamicity and fibrous structure is of great interest in regenerative medicine. However, such hydrogels generally have weak mechanical properties and poor structural stability, which significantly limits their potential applications. To overcome this drawback, we developed a new type of hybrid network composed of supramolecular assemblies with covalent nanoparticle-based crosslinkers. The ECM mimetic hydrogels were created through UV-initiated thiol-ene crosslinking between norbornene functionalized benzene-1,3,5-tri carboxamide (NBTA) macromonomers and thiol functionalized mesoporous silica nanoparticles (MSN). We hypothesized that the MSN would improve the mechanical properties by crosslinking the NBTA supramolecular fibrous hydrogels. Notably, the covalent incorporation of MSNs did not disrupt the fibrous morphology of the resulting NBTA-MSN nanocomposites. Furthermore, these supramolecular nanocomposites demonstrated higher structural stability and elasticity compared to pristine NBTA hydrogels. Rheology studies showed that the mechanical properties of NBTA-MSN hydrogels could be tuned by adjusting MSN wt%. Interestingly, NBTA-MSN nanocomposites exhibited self-healing and injectability despite the covalent crosslinking of MSNs. In vitro studies confirmed that NBTA-MSN nanocomposites showed good cytocompatibility and maintained the viability of encapsulated MG63 cells. As a proof of concept, we also demonstrated that MSNs could act as ion reservoirs for calcium and phosphate within the hydrogel networks in addition to being covalent crosslinkers. Taken together, our work offers a promising strategy to create hybrid, biomimetic supramolecular nanocomposite materials for various applications such as injectable materials for bone tissue engineering, and reinforced bioinks for 3D printing applications.

Fishing net-inspired PVA-chitosan-CNT hydrogels with high stretchability, sensitivity, and environmentally stability for textile strain sensors

Soft electronic products are being extensively investigated in diverse applications including sensors and devices, due to their superior softness, responsiveness, and biocompatibility. One-dimensional (1-D) fiber electronic devices are recognized for their lightweight, wearable, and stretchable qualities, thus emerging as critical constituents for seamless integration with the human body and attire, exhibiting great potential in wearable applications. However, wearable conductive hydrogel fibers usually face challenges in combining stretchability and excellent stability, notably in high-temperature environment. Herein, a novel stretchable conductive hydrogel fiber, namely PVA-CS-CNT (Polyvinyl Alcohol-Chitosan-Carbon Nanotube) hydrogel fiber, was successfully prepared through a straightforward low-temperature process. This hydrogel fiber not only maintains stable signal transmission at high temperatures but also exhibits significant mechanical and sensing capabilities, ensuring signal stability during repetitive cyclic stretching. Inspired by fishing net, textile sensors were fabricated by weaving PVA-CS-CNT hydrogel fibers, which offered breathability, high stability (withstanding over 500 stretch cycles), high sensitivity (detecting strains as low as 1 %), and exceptional mechanical strength (exceeding 17 MPa). The wearable sensor could not only accurately monitor human movements like stretching and bending, but also adeptly captured delicate signals such as pulses and sounds. These characteristics demonstrated the potential applications of the hydrogel fibers encompassing human motion tracking, intelligent textiles, and soft robotics.

Continuous Phase Separation Induced Tough Hydrogel Fibers with Ultrahigh Conductivity for Multidimensional Soft Electronics

AbstractConductive hydrogel fibers exhibit great potential in soft robots, bioelectronics, and human–machine interfaces due to the unique combination of electrical conductivity, high water content, tissue‐like mechanical properties, and 1D structure. Despite significant advances in hydrogel technologies, the typical conductive hydrogel fibers show low conductivity (<10 S cm−1), weak mechanical properties, and water stability, which makes it challenging to satisfy the requirements of practical applications. Here, a facile strategy is proposed to construct hydrogel fibers with ultrahigh conductivity and toughness by exploiting the synergistic effects of freezing‐thawing, salting‐out, and drying‐annealing. The continuous phase separation induced by the combined processes results in hierarchical structures, promoting the formation of interconnected conductive networks and increasing the fiber's crystallinity and crystal domain size. The prepared conductive hydrogel fibers exhibited ultrahigh conductivity (≈958 S cm−1), excellent mechanical properties (strength (≈6.2 MPa), stretchability (>300%), and toughness (≈10 MJ m−2)), high water content (≈75%), outstanding water stability, and fatigue resistance properties. In addition, the processibility of conductive hydrogel yarns and fabrics are demonstrated and their potential application in bioelectronics. Overall, this work presents a preparation strategy for conductive hydrogel fibers, which will facilitate the advancement of soft electronics and may inspire structural construction in other polymers.

Super Strong and Tough PVA Hydrogel Fibers Based on an Ordered‐to‐Disordered Structural Construction Strategy Targeting Artificial Ligaments

AbstractHydrogels with high strength, high modulus, and high toughness have great application potential in the field of artificial human load‐bearing tissues, but the preparation of materials with the above high performance is still a huge challenge. In this paper, a structural construction strategy of ordered‐to‐disordered (OTD) transition is proposed to obtain hydrogel fibers with high strength, high modulus, and high toughness. The structural construction strategy of OTD refers to the ordered‐to‐disordered transition of molecular segments in PVA polymer fibers through swelling and subsequent salting‐out treatment, while still maintaining the general order of the entire polymer chain. PVA molecular chain crystallites provide physical crosslinking to stabilize the structure. The results show that the elongation at break of the hydrogel fiber can reach 257%). The strength reaches 190.04 MPa, which is more than 4 times higher than that of human ligaments. The modulus reaches 137.31 MPa, which perfectly matches the human ligaments, and the toughness can reach 100.61 MJ m−3. In addition, it has stable mechanical properties in liquid environment and excellent biocompatibility, which has great application potential in the field of artificial ligaments. This OTD structural construction strategy provides a facile approach to achieving hydrogel fibers with desired mechanical properties.

Glutaraldehyde Cross-Linking of Salt-Induced Fibrinogen Hydrogels.

Covalent cross-linking is a common strategy to improve the mechanical properties of biological polymers. The most prominent field of application of such materials is in medicine, for example, in the form of bioprinting, drug delivery, and wound sealants. One biological polymer of particular interest is the blood clotting protein fibrinogen. In the natural process, fibrinogen polymerizes to fibrous hydrogel fibrin. Although the material shows great potential, its costs are very high due to the required enzyme thrombin. Recently, we introduced several approaches to trigger a thrombin-free fibrillogenesis of fibrinogen to a fibrin-like material. Inspired by the natural pathway of blood clotting in which covalent cross-linking stabilizes the clot, this "pseudofibrin" is now developed even further by covalently cross-linking the fibers. In particular, the effect of inexpensive glutaraldehyde on fiber morphology, rheological properties, and irreversible gel dissolution is investigated. Additionally, new insights into the reaction kinetics between fibrinogen and glutaraldehyde are gained. It could be shown that the fibrous structure of pseudofibrin can be retained during cross-linking and that glutaraldehyde significantly improves rheological properties of the hydrogels. Even more important, cross-linking with glutaraldehyde can prevent dissolution of the gels at elevated temperatures.

Continuous Preparation of the Record Strength and Toughness Hydrogel Fibers with a Homogeneous Crosslinked Network by Microcrystalline Dispersed Growth

Continuous Preparation of the Record Strength and Toughness Hydrogel Fibers with a Homogeneous Crosslinked Network by Microcrystalline Dispersed Growth

Scalable Layered Heterogeneous Hydrogel Fibers with Strain-Induced Crystallization for Tough, Resilient, and Highly Conductive Soft Bioelectronics.

The advancement of soft bioelectronics hinges critically on the electromechanical properties of hydrogels. Despite ongoing research into diverse material and structural strategies to enhance these properties, producing hydrogels that are simultaneously tough, resilient, and highly conductive for long-term, dynamic physiological monitoring remains a formidable challenge. Here, a strategy utilizing scalable layered heterogeneous hydrogel fibers (LHHFs) is introduced that enables synergistic electromechanical modulation of hydrogels. High toughness (1.4MJ m-3) and resilience (over 92% recovery from 200% strain) of LHHFs are achieved through a damage-free toughening mechanism that involves dense long-chain entanglements and reversible strain-induced crystallization of sodium polyacrylate. The unique symmetrical layered structure of LHHFs, featuring distinct electrical and mechanical functional layers, facilitates the mixing of multi-walled carbon nanotubes to significantly enhance electrical conductivity (192.7 S m-1) without compromising toughness and resilience. Furthermore, high-performance LHHF capacitive iontronic strain/pressure sensors and epidermal electrodes are developed, capable of accurately and stably capturing biomechanical and bioelectrical signals from the human body under long-term, dynamic conditions. The LHHF offers a promising route for developing hydrogels with uniquely integrated electromechanical attributes, advancing practical wearable healthcare applications.

An optical system for cellular mechanostimulation in 3D hydrogels

We introduce a method utilizing single laser-generated cavitation bubbles to stimulate cellular mechanotransduction in dermal fibroblasts embedded within 3D hydrogels. We demonstrate that fibroblasts embedded in either amorphous or fibrillar hydrogels engage in Ca2+ signaling following exposure to an impulsive mechanical stimulus provided by a single 250 µm diameter laser-generated cavitation bubble. We find that the spatial extent of the cellular signaling is larger for cells embedded within a fibrous collagen hydrogel as compared to those embedded within an amorphous polyvinyl alcohol polymer (SLO-PVA) hydrogel. Additionally, for fibroblasts embedded in collagen, we find an increased range of cellular mechanosensitivity for cells that are polarized relative to the radial axis as compared to the circumferential axis. By contrast, fibroblasts embedded within SLO-PVA did not display orientation-dependent mechanosensitivity. Fibroblasts embedded in hydrogels and cultured in calcium-free media did not show cavitation-induced mechanotransduction; implicating calcium signaling based on transmembrane Ca2+ transport. This study demonstrates the utility of single laser-generated cavitation bubbles to provide local non-invasive impulsive mechanical stimuli within 3D hydrogel tissue models with concurrent imaging using optical microscopy. Statement of significanceCurrently, there are limited methods for the non-invasive real-time assessment of cellular sensitivity to mechanical stimuli within 3D tissue scaffolds. We describe an original approach that utilizes a pulsed laser microbeam within a standard laser scanning microscope system to generate single cavitation bubbles to provide impulsive mechanostimulation to cells within 3D fibrillar and amorphous hydrogels. Using this technique, we measure the cellular mechanosensitivity of primary human dermal fibroblasts embedded in amorphous and fibrillar hydrogels, thereby providing a useful method to examine cellular mechanotransduction in 3D biomaterials. Moreover, the implementation of our method within a standard optical microscope makes it suitable for broad adoption by cellular mechanotransduction researchers and opens the possibility of high-throughput evaluation of biomaterials with respect to cellular mechanosignaling.

Dynamic Adhesive Fibers for Remote Capturing of Objects

AbstractB. mori silk has been extensively utilized to create Regenerated Silk Fibroin solutions (RSF) for a wide range of technological applications, including tissue engineering, drug delivery, biomaterials, and adhesives. In this study, an RSF‐dopamine (DA) composite is introduced that yields easily deployable hydrogel fibers possessing adhesive properties that can be released on demand to capture and retrieve loads from a distance. The RSF‐DA serves as an artificial dope, combining the functional attributes of silk fibroin (i.e., hydrogel formation) and dopamine (i.e., adhesion) to instantly generate adjustable hydrogel fibers displaying a sticky behavior. The mechanical strength and adhesive characteristics of this material are assessed using tensile and lap‐shear tests. Furthermore, the possibility of tuning these properties is demonstrated by adding chitosan (Ch) and borate ions (BB), leading to remarkable mechanical and adhesive performances up to 107 MPa and 280 kPa, respectively, which allows the retrieval of objects from the ejected structure. This process can be finely tuned to achieve a controlled fabrication of instantaneously formed adhesive hydrogel fibers for manifold applications, mimicking living organisms’ ability to eject tunable adhesive functional threads.

Fortifying the foundation: assessing the role of uterine ligament integrity in uterine prolapse and beyond.

Pelvic floor stability is influenced by various biomechanical, anatomical, and physiological factors. Understanding these dynamics is crucial for improving the treatment of pelvic organ prolapse (POP) and related conditions. To analyze the key factors affecting pelvic floor integrity and explore both non-surgical and surgical interventions to enhance stability and treatment outcomes. This review draws from biomechanical research to assess the role of the uterosacral ligament in pelvic support, while also examining the potential of both traditional and emerging therapeutic approaches, including non-surgical interventions like vitamin C supplementation. - The uterosacral ligament demonstrates superior strength and stiffness, making it essential for structural support of pelvic organs. - Non-surgical interventions, such as vitamin C supplementation, show potential in improving ligament integrity and preventing pelvic floor disorders. - Emerging surgical techniques, including tendon-based procedures and injectable fibrous hydrogel composites, offer promising improvements in outcomes for patients with pelvic organ prolapse. - Additional factors such as muscle strength and neural deficiencies contribute to the complexity of pelvic floor biomechanics, indicating the need for multifaceted treatment approaches. This analysis provides a comprehensive framework for understanding and managing pelvic floor stability by integrating biomechanical, physiological, and anatomical insights. The findings highlight the potential for personalized treatment strategies to improve patient outcomes in pelvic floor disorders.

“Bamboo-like” strong and tough sodium alginate/polyacrylate hydrogel fiber with directional controlled release for wound healing promotion

Skin, as the biggest organ and outermost surface of the human body, is prone to injury due to various challenges, especially the expanding potential of accidents, which bring a huge social and economic burden. Hydrogels are emerging as the most promising candidate for wound dressings, which not only fulfill the varied requirements of dressings but also serve as drug carriers. But limited breathability, rapid drug release, and inadequate mechanical properties remains a significant challenge. Herein, we report a strong and tough sodium alginate/polyacrylate hydrogel fibers-based dressing with directional controlled drug release for wound healing promotion. Mimicking the bamboo structure, the drug solution is encapsulated within the fiber, and the rate of drug release can be modulated by controlling the wall thickness of the fiber. A cross-network structure in the hydrogel fiber through hydrogen bond and calcium ion crosslinking resulted in a 38 % increase in tensile strength. By precisely controlling the feeding process during weaving, drug-loaded fibers can be prepared at specific locations to facilitate targeted delivery to skin wound sites. Drug-loaded fabric has the breathability and biocompatibility required for dressings to promote wound healing. The findings highlight the potential of alginate/polyacrylate hydrogel fabrics for effective wound treatment.

Facile Formation of Multifunctional Biomimetic Hydrogel Fibers for Sensing Applications.

To face the challenges in preparing hydrogel fibers with complex structures and functions, this study utilized a microfluidic coaxial co-extrusion technique to successfully form functional hydrogel fibers through rapid ionic crosslinking. Functional hydrogel fibers with complex structures, including linear fibers, core-shell structure fibers, embedded helical channels, hollow tubes, and necklaces, were generated by adjusting the composition of internal and external phases. The characteristic parameters of the hydrogel fibers (inner and outer diameter, helix generation position, pitch, etc.) were achieved by adjusting the flow rate of the internal and external phases. As biocompatible materials, hydrogel fibers were endowed with electrical conductivity, temperature sensitivity, mechanical enhancement, and freeze resistance, allowing for their use as temperature sensors for human respiratory monitoring and other biomimetic application developments. The hydrogel fibers had a conductivity of up to 22.71 S/m, a response time to respiration of 37 ms, a recovery time of 1.956 s, and could improve the strength of respiration; the tensile strength at break up to 8.081 MPa, elongation at break up to 159%, and temperature coefficient of resistance (TCR) up to -13.080% °C-1 were better than the existing related research.

Strong and anti-swelling nanofibrous hydrogel composites inspired by biological tissue for amphibious motion sensors.

Conductive hydrogel-based sensors are increasingly favored for flexible electronics due to their skin-like characteristics. However, conventional hydrogels suffer from significant swelling in humid environments and poor mechanical properties which largely restrict their applications in wearable electronic devices, especially for underwater sensing. Herein, drawing inspiration from the extracellular matrix (ECM) structure, a TPU-PVAc@AgNPs/MXene nanofibrous hydrogel composite (TPAMH) with excellent mechanical robustness and anti-swelling properties is developed. The TPAMH nanofibrous hydrogel composite is created by integrating the silver nanoparticles (AgNPs) and MXene nanosheets into an interwoven network comprising of stiff TPU nanofibers as the fibril scaffold and formic acid-crosslinked PVA hydrogel fibers as the elastic matrix (PVAc). Benefiting from the unique ECM structure, the obtained nanofibrous hydrogel composites exhibit exceptional tensile strength (4.47 MPa), remarkable elongation at break (621%), excellent anti-swelling properties, and high detection sensitivity (maximum gauge factor = 105.02), which are sufficient to monitor body motions in both air and water environments effectively. They can detect large strain movements of fingers, elbows, wrists, and knees, as well as small strain physiological signals such as frown, smile, and pulse beats, with high accuracy. Particularly noteworthy is their ability to accurately identify underwater multidirectional motions and facilitate underwater smart alarms using Morse code.

Stable Persistent Room-Temperature Phosphorescent Hydrogels Based on Ionically Crosslinked Nonaromatic Carboxylate Polymers.

Developing pure organic room-temperature phosphorescent (RTP) hydrogels is important for expanding the practical applications of phosphorescent materials. However, most of the reported RTP hydrogels containing aromatic phosphors suffer from short phosphorescent lifetimes, unstable underwater RTP emissions, and complex preparation processes. Herein, novel nonaromatic RTP hydrogels are prepared by using two types of non-traditional luminescent polymers, sodium alginate and a polymeric carboxylate, which are not RTP emissive or very weakly emissive in aqueous environments. The prepared hydrogels exhibit the following features: I) color-tunable RTP emissions with ultra-long lifetimes up to 451.1ms, II) excellent anti-swelling properties and stable persistent RTP emission even after being immersed in deionized water for months, III) efficient and large-scale preparation of hydrogel fibers by wet spinning technique. Experiment results and theoretical calculations show that the stable and long-lifetime RTP emissions of the hydrogels originate from the introduction of more nonconventional chromophores which are strongly crosslinked with ionic bonding between carboxylate groups and calcium ions and enhanced through-space interactions between them. This work provides a reliable strategy for designing nonaromatic hydrogels with stable and persistent RTP.

Design, application, and recycling of zinc alginate/guar gum hydrogel-based fibers

Extreme cold events are quite common, highlighting the urgent need for flexible wearable electronic devices capable of diagnosing human health in low-temperature environments. Using a wet spinning strategy, we successfully developed sodium zinc alginate/guar gum(SZA/GG) hydrogel fibers with excellent environmental resistance, antimicrobial properties, and electrical conductivity. Building on this, we developed a flexible wearable sensing device that operates stably at low temperatures and exhibits a sensitivity of 0.585 within the range of −20 °C to −40 °C, demonstrating excellent response performance. When evaluating the physical state of outdoor athletes, the amplitude and fluctuation range of electrical resistance provide valuable information about the monitored environment and the risk of frostbite for the individual. However, like any device, it eventually reaches its usage limit. To address the issue of recycling hydrogel fiber waste, we propose recycling and carbonizing the discarded devices to use as a biomass carbon source for fabricating button-type supercapacitors. After 10,000 charge-discharge cycles, the capacitance retention rate reached 92.53 %, demonstrating the potential of these supercapacitors and offering a new approach to reducing resource waste.

Coaxial Bioprinting of Enzymatically Crosslinkable Hyaluronic Acid-Tyramine Bioinks for Tissue Regeneration.

Three-dimensional (3D) bioprinting has emerged as an important technique for fabricating tissue constructs with precise structural and compositional control. However, developing suitable bioinks with biocompatible crosslinking mechanisms remains a significant challenge. This study investigates extrusion-based bioprinting (EBB) using uniaxial or coaxial nozzles with enzymatic crosslinking (EC) to produce 3D tissue constructs in vitro. Initially, low-molecular-weight dextran-tyramine and hyaluronic acid-tyramine (LMW Dex-TA/HA-TA) bioink prepolymers were evaluated. Enzymatically pre-crosslinking these prepolymers, achieved by the addition of horseradish peroxidase and hydrogen peroxide, produced viscous polymer solutions. However, this approach resulted in inconsistent bioprinting outcomes (uniaxial) due to inhomogeneous crosslinking, leading to irreproducible properties and suboptimal shear recovery behavior of the hydrogel inks. To address these challenges, we explored a one-step coaxial bioprinting system consisting of enzymatically crosslinkable high-molecular-weight hyaluronic acid-tyramine conjugates (HMW HA-TA) mixed with horseradish peroxidase (HRP) in the inner core and a mixture of Pluronic F127 and hydrogen peroxide in the outer shell. This configuration resulted in nearly instantaneous gelation by diffusion of the hydrogen peroxide into the core. Stable hydrogel fibers with desirable properties, including appropriate swelling ratios and controlled degradation rates, were obtained. The optimized bioink and printing parameters included 1.3% w/v HMW HA-TA and 5.5 U/mL HRP (bioink, inner core), and 27.5% w/v Pluronic F127 and 0.1% H2O2 (sacrificial ink, outer shell). Additionally, optimal pressures for the inner core and outer shell were 45 and 80 kPa, combined with a printing speed of 300 mm/min and a bed temperature of 30 °C. The extruded HMW HA-TA core filaments, containing bovine primary chondrocytes (BPCs) or 3T3 fibroblasts (3T3 Fs), exhibited good cell viabilities and were successfully cultured for up to seven days. This study serves as a proof-of-concept for the one-step generation of core filaments using a rapidly gelling bioink with an enzymatic crosslinking mechanism, and a coaxial bioprinter nozzle system. The results demonstrate significant potential for developing designed, printed, and organized 3D tissue fiber constructs.

Engineering Supramolecular Hydrogels via Reversible Photoswitching of Cucurbit[8]uril-Spiropyran Complexation Stoichiometry.

The integration of photoswitchable supramolecular units into hydrogels allows for spatiotemporal control over their nanoscale topological network and macroscale properties using light. Nevertheless, the current availability of photoswitchable supramolecular interactions for the development of such materials remains limited. Here, the molecular design of a novel photoswitchable cucurbit[8]uril-spiropyran host-guest complex exhibiting fast and reversible switching of binding ratios between 1:2 and 1:1 is reported. Photoswitchable complexation stoichiometries are rationally exploited as (de)crosslinking units in multiple polymers for the design of supramolecular hydrogels displaying highly dynamic and switchable features that are spatiotemporally controlled by light. The hydrogels exhibit rapid reversible mechanical softening-hardening upon alternating irradiation with blue and UV light, which is used to significantly accelerate and improve the efficiency of self-healing and shape-remolding of hydrogels. Furthermore, spiropyran endows such materials with unique reversible photochromic properties for reproducible patterning/erasing and information storage. Using a dual-light-assisted extrusion process, meter-scale hydrogel fibers with enhanced structural integrity and photoswitchable ionic conductivity are constructed and woven into various slidable knots and fluorescent shapes. This work represents an innovative molecular design strategy for advancing the development of spatiotemporally engineered supramolecular hydrogels using light and opens avenues for their prospective applications in dynamic materials and adaptive systems.

Enhanced interface bonding of hydrophobic encapsulated hydrogel fibers by mechanical interlocking structure: Toward anti-drying and anti-swelling strain sensors

Conductive hydrogel fibers with superior mechanical and electrical performance have been developed for flexible wearable electronics, but the inherent properties of hydrogels for dehydration in the atmosphere and underwater swelling limit its widespread application. In this work, a silicone rubber encapsulated hydrogel fiber with enhanced interface bonding, excellent mechanical and electrical properties was successfully developed, in which the core polyvinyl alcohol/sodium alginate hydrogel fiber was prepared by a continuous wet-spinning and the following freeze-thawing. The interlocking dual-network structure and the improved ion transport by negatively charged sodium alginate gave the core hydrogel fiber excellent strength of 4.15 MPa, elongation-at-break of 1531 % and electrical conductivity of 17.01 S·m−1. After encapsulation using a silicone rubber, the composite hydrogel fiber showed a low expansion rate underwater for 7 days of 1.00 ± 0.21 % and low weight loss in the air over 36 h of 38.67 ± 0.38 %. And the interface bonding of the core hydrogel fiber and silicone layer was enhanced by the bridging effect of amphiphilic stearic acid. Therefore, the composite hydrogel fiber demonstrated a great potential as a strain sensor for underwater communication to ensure the safety of individuals in an underwater environment.

Injectable interface-bonded fiber-reinforced thiolated chitosan hydrogels for enhanced cellular activities and cartilage regeneration

Injectable hydrogels with heterogeneous fibrous structures possessing good mechanical and biological characteristics are attracting increasing research interest in cartilage repair. The integration of nanofibers into hydrogel would largely enhance mechanical property, but impedes the gelation process and formation of hydrogel structures. Construction of biocompatible and mechanical supporting hydrogel with low fiber content remains a challenge. In this study, we developed a chemical cross-linked fibrous hydrogel, namely Thiol chitosan-Poly (lactic-co-glycolic acid)-Polydopamine (CSSH-PP), for facilitating cell proliferation and promoting cartilage tissues regeneration. Compared to conventional CSSH hydrogels, the compressive strength of CSSH-PP scaffolds exhibited a significant increase percentage of 100 %. Incorporation of CSSH-PP upgraded the cell migration with a four-fold increase. Besides, the infiltration of host cells and the formation of new blood vessels were observed in rat models when implanted with CSSH-PP, enhancing the native tissue microenvironmental reconstruction and leading a sustained repair in articular cartilage.