REVIEW article

Front. Cell Dev. Biol., 14 November 2024

Sec. Cell Adhesion and Migration

Volume 12 - 2024 | https://doi.org/10.3389/fcell.2024.1499766

Adhesive chitosan-based hybrid biohydrogels for peripheral nerve injury repair

  • PQ

    Pengjia Qiu 1

  • LW

    Lei Wang 1

  • JW

    Jing Wang 1

  • XW

    Xingdong Wang 2

  • JX

    Jianchao Xu 1

  • XA

    Xiaokai An 1

  • FH

    Fengwang Han 1

  • ZD

    Zhao Dong 1

  • JZ

    Jiangtao Zhang 1

  • PS

    Peiwen Shi 1

  • QN

    Qiang Niu 1*

  • 1. Department of Orthopedics, Gaoyang County Hospital, Baoding, Hebei Province, China

  • 2. Department of Orthopedics, Sichuan Gemflower Hospital, North Sichuan Medical College, Sichuan, China

Abstract

With the rapid progress of industrialization, the incidence of peripheral nerve injuries caused by trauma has been continuously increasing. These injuries result in a significant number of disabilities and irreversible functional impairments, not only severely impacting the health and quality of life of patients but also placing a heavy economic burden on families and society. Effectively promoting peripheral nerve regeneration has thus become a key focus and challenge in current research. In recent years, hybrid biohydrogels with adhesive properties have gained widespread attention due to their excellent biocompatibility, mechanical stability, conductivity, and biodegradability. These materials can provide an optimal microenvironment to promote neuron adhesion and axonal extension while offering outstanding mechanical strength to meet the fixation requirements in clinical surgeries. This paper systematically reviews the application of adhesive hybrid biohydrogels in peripheral nerve injury repair, highlighting the latest research progress in promoting nerve regeneration and improving functional recovery, and discusses the challenges and future prospects for their clinical application.

1 Introduction

With the increasing number of traffic accidents, medical accidents, and the rapid expansion of mechanized production, traumatic peripheral nerve injury occurs more frequently (; ; ). Once it happens, it may lead to sensory and motor dysfunction, seriously affect the body’s function and daily life, and cause significant burden and pressure on social and personal life. The structure and function of human nerve tissue are complex and changeable, so it is difficult to repair completely (; Liu et al, 2022). Clinically, the first choice for treating peripheral nerve injury is a tension-free epineural suture after docking short-distance injured nerves under microsurgery (Pauchot et al., 2017). For long-distance peripheral nerve injuries, autologous and allogeneic nerve grafts are generally used (; ; ; ; Wang et al., 2021). The disadvantages of autologous nerve transplantation are limited nerve source, easy damage or permanent loss of donor function, limited repairable length, long operation time, the low success rate of transplantation, the emergence of the painful neuroma, and so on (; Wilson, 2021). Autogenous nerve transplantation still does not achieve satisfactory results in clinical repair and will still produce serious complications (; Sebben et al., 2011). Similarly, allogeneic nerve transplantation is more likely to appear immune and rejected, which is not conducive to recovery from peripheral nerve sensation and function (; ). Therefore, many researchers use hybrid biohydrogels to repair peripheral nerves (; Ma et al., 2021; Uranues et al., 2020). They were hoping to develop a perfect material to repair peripheral nerve injury to alleviate the pain of patients. Through the efforts of many experts and scholars, a variety of nerve substitute materials have been found.

Adhesive chitosan-based hybrid biohydrogels are currently a focal point in the treatment of peripheral nerve injuries due to their unique properties and therapeutic potential. These hydrogels are composed of chitosan, a biocompatible polymer, integrated with other biomaterials to form a supportive, adhesive matrix. The primary advantage of these hydrogels lies in their ability to promote neuronal cell regeneration and provide sustained release of growth factors or pharmaceuticals directly at the injury site (Figure 1). This dual functionality not only accelerates nerve repair but also reduces the need for microsurgical suturing, thereby simplifying the surgical process. The adhesive nature of these hydrogels ensures close contact with nerve tissues, facilitating better integration and reducing the mechanical stress typically associated with conventional nerve repair techniques. This innovative approach is transforming the way peripheral nerve injuries are treated, offering a less invasive and more efficacious alternative to traditional methods.

FIGURE 1

2 Chitosan-based hybrid biohydrogels

Chitosan-based hybrid biohydrogels have demonstrated multiple innovative designs in the field of tissue engineering and regenerative medicine, making them a current research focus. First, by incorporating conductive materials such as graphene, carbon nanotubes, or conductive polymers with chitosan, conductive hydrogels are formed, which can effectively promote tissue repair under electrical stimulation, particularly showing remarkable results in nerve and cardiac tissue regeneration (; ; Teng et al., 2023). Moreover, chitosan hydrogels can load growth factors, such as basic fibroblast growth factor (bFGF) or vascular endothelial growth factor (VEGF), to regulate cell proliferation and differentiation, thereby enhancing tissue regeneration (; ; Liu et al, 2022; Rao et al., 2020). At the same time, chitosan-based hydrogels are capable of loading stem cells, such as mesenchymal stem cells (MSCs) or neural stem cells (NSCs), providing a three-dimensional scaffold to maintain cell viability and further improve tissue repair outcomes (; Liu et al, 2020; Mahya et al., 2021; Salehi et al., 2019). These innovative designs not only enhance the adaptability of chitosan hydrogels in complex biological environments but also significantly expand their potential applications in various tissue repair fields, demonstrating promising prospects for the future.

2.1 Conductive hybrid biohydrogel

Conductive hybrid biohydrogels offer a significant advantage in peripheral nerve injury repair due to their ability to facilitate bioelectrical signal transmission, a crucial factor in nerve regeneration. As shown in Figure 2, The incorporation of conductive materials, such as polypyrrole, graphene, or carbon nanotubes, allows these hydrogels to replicate the native electrical conductivity of nerve tissues, which is essential for maintaining neuronal communication and promoting axonal growth (; Lu et al., 2014; Ng et al., 2020). This electrical conductivity enhances cell signaling pathways that regulate Schwann cell activity, myelination, and synaptic plasticity, all of which are critical for functional nerve recovery (Runge et al., 2010; Yang et al., 2019). Moreover, conductive hydrogels can provide electrical stimulation to the injury site, further boosting cell proliferation and accelerating tissue regeneration (; ; Wu et al, 2020). Compared to non-conductive hydrogels, the conductive variants significantly improve both the speed and quality of nerve repair, offering a more effective solution for clinical applications. This innovative design approach not only promotes biological integration but also supports the long-term functionality of the regenerated nerve, addressing key limitations of current repair strategies.

FIGURE 2

). Reprinted (adapted) with permission from {Applied Materials}. Copyright {2021} American Chemical Society.

2.2 Hybrid biohydrogel with growth factors

Hybrid hydrogels loaded with growth factors have shown great potential in repairing peripheral nerve injuries (PNI) due to their ability to provide a bioactive scaffold that mimics the natural extracellular matrix. Growth factors such as nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and glial cell-derived neurotrophic factor (GDNF) are essential in promoting neural survival, axonal growth, and remyelination (; Yan et al., 2012). Loading these factors into hydrogels enables their controlled and sustained release, creating an optimal environment for nerve regeneration over extended periods. This design feature significantly enhances therapeutic outcomes by preventing the rapid degradation of growth factors and ensuring their availability at the injury site (). Furthermore, the hybrid nature of the hydrogels, combining both natural and synthetic polymers, provides enhanced mechanical strength, biocompatibility, and degradation rates, which are critical for adapting to the dynamic environment of peripheral nerve tissues () (Figure 3A). The combination of these properties allows for the functional restoration of damaged nerves, making growth factor-loaded hybrid hydrogels a highly effective platform for PNI repair.

FIGURE 3

).

2.3 Hybrid biohydrogel with stem cells

Hybrid hydrogels loaded with stem cells have emerged as an innovative solution for peripheral nerve injury (PNI) repair due to their ability to deliver regenerative cells in a controlled and supportive environment. Stem cells, such as mesenchymal stem cells (MSCs) or neural stem cells (NSCs), are known for their capacity to differentiate into various cell types, including neurons and Schwann cells, which are essential for nerve regeneration (). As illustrated in Figure 3B, by embedding stem cells within hydrogels, researchers can ensure localized delivery and protection of these cells, preventing their rapid degradation or immune rejection (). This controlled release system enhances cell survival, proliferation, and differentiation at the injury site, leading to improved nerve repair outcomes. Hybrid hydrogels, which combine natural and synthetic polymers, offer advantages in terms of mechanical stability, biocompatibility, and tailored degradation rates (Li et al., 2014). This allows the hydrogel to gradually degrade as the nerve tissue regenerates, reducing the need for surgical removal (). The combination of stem cell delivery and the supportive scaffold properties of the hydrogel makes this approach a highly effective strategy for enhancing functional nerve recovery in PNI.

3 Adhesive between hydrogel and epineurial tissue

The epineurium covers the surface of nerve axons, and the adhesive properties of the interface between the hydrogel and the epineurium directly influence the effectiveness and biocompatibility of its application in the aforementioned areas. Since the 1980s, epineural adhesives have been developed to adhere to nerve surfaces for drug delivery. Common epineural adhesives include polyacrylates, alginates, chitosan, and cellulose derivatives. They are processed into dry forms (tablets, films, and patches) and wet forms (hydrogels and ointments). When hydrogel adhesives come into contact with the epineurium, the polymer chains within the hydrogel interpenetrate with the glycoproteins in the mucosa, allowing the hydrogel adhesive to tightly adhere to the epineurium. Therefore, robust interfacial adhesion between the hydrogel and epineural tissue is one of the key factors ensuring the overall stability and reliability of the hydrogel during its application.

3.1 Chemical structure adhesion interface

Biohydrogels can be bridged to the epineurium through the inclusion of specific chemical structures, such as catechol or other substances that contain catechol groups, such as epigallocatechin gallate (EGCG) and tannic acid (TA).

In 1981, Waite and Tanzer first discovered a catechol-based adhesion mechanism in the adhesive feet of mussels (Waite and Tanzer, 1981). Subsequently, many adhesives containing phenolic components were reported (Figure 4) (Yang et al., 2021; Zhou et al., 2021), but most of these adhesives could only adhere in dry conditions and were not suitable for moist environments filled with tissue fluids found inside the body (; Priemel et al., 2021). Catechol plays a crucial role in adhesion, and the synergistic action between various amino acids and catechol in the adhesive proteins of mussels and sandcastle worms makes underwater adhesion possible. For example, during the secretion process of the sandcastle worm’s glue, the pH shifts from weakly acidic to weakly alkaline, prompting the gradual oxidation of dopamine (DOPA) to DOPA-quinone, which accelerates the cohesive process of the adhesive proteins. The metal ions in seawater form complexes with the adhesive proteins, speeding up the curing of the adhesive. The hydrophobicity of the insoluble complex aggregates aids in water displacement, increasing the contact between the adhesive proteins and the substrate. The final adhesion is achieved through the interactions between dopamine and the substrate.

FIGURE 4

In recent years, researchers have delved into the adhesion mechanisms of mussels in wet environments and the properties of their adhesive proteins. The foot proteins Mfp-5 and Mfp-3 secreted by the mussel’s foot, located at the plaque surface, contain abundant DOPA and play a crucial role in underwater adhesion. The complexation and oxidation of catechol oxidase with DOPA, along with the marine weakly alkaline environment, increase the crosslinking density and cohesive strength of the adhesive. Unreacted dopamine adheres to substrates in water through various interactions. Additionally, the catechol groups undergo covalent auto-crosslinking under oxidizing conditions, significantly enhancing the cohesive strength of wet adhesives, while catechol groups help form a protein coagulation layer with excellent wettability on all substrates immersed in water. Recent studies have also found that catechol groups promote self-assembly through cation-π interactions and hydrogen bonding (Zhang et al, 2020), which facilitate instant adhesion and polymer coagulation.

3.2 Physical structure adhesion interface

In addition to adhesion based on catechol-related chemical bonds, mimicking mussels, and sandcastle worms, there are also examples of physical structure adhesion in nature, such as those found in geckos (; Tian et al., 2006), octopuses (; ), tree frogs (), and other insects (Liu et al, 2021). In recent years, the mechanism of adhesion formed by specially designed physical structures has received unprecedented attention, and many related studies have been published (Li et al., 2024). Adhesives can adhere to different surfaces through van der Waals forces, electrostatic forces, and hydrophobic/hydrophilic interactions.

Geckos can move freely on smooth surfaces because they provide strong and reversible adhesion on surfaces with varying roughness and orientation. This extraordinary adhesion ability is due to the millions of tiny setae (bristles) on gecko feet, which are divided into hundreds of even smaller nanoscale tips (spatulae). These tips form intimate contact with various surfaces through van der Waals forces, resulting in a strong adhesive force (approximately 10 N/cm2) (). Xue et al., inspired by gecko feet, designed and fabricated a polydimethylsiloxane (PDMS) micropillar array with radially oriented conical tips (PROST). By mimicking the unique movement pattern of gecko toes, PROST achieved excellent adhesion on both flat and spherical surfaces, with up to 150 adhesion cycles (Shi et al., 2022).

Octopuses can firmly adhere to the rocks on the ocean floor and move swiftly. Their outstanding adhesive ability primarily depends on their suckers, which enable their tentacles to attach to foreign surfaces and achieve flexible control and reversible movement with strong adhesive strength. Based on the adhesion mechanism of octopus suckers, Lee et al. designed a smart adhesive pad that can be actively controlled through a thermal-responsive drive, achieving reversible adhesion by adjusting the pressure difference inside and outside the pad cavity.

Tree frogs can firmly adhere to and successfully climb soft leaves, attributed to the specialized microstructures on the soles of their feet. These microstructures are composed of hexagonal epithelial cells, each side measuring 10 μm, separated by tiny channels (2 μm wide). These channels exhibit omnidirectional peel resistance as well as drainage on wet and rough surfaces, enabling direct contact for efficient adhesion (Figure 5) (; Liu et al, 2021). Xue et al., inspired by the structure of tree frog toes, designed a composite micropillar array with nanoscale pits on the surface. When pressure is applied, its adhesive force can reach 36.5 times that of tree frog toe pads (Liu et al, 2020).

FIGURE 5

).

The clingfish exhibits fast and reversible adhesion to various underwater substrates due to the presence of a suction disc with a hexagonal pattern separated by interconnected grooves, which enhances drainage capability. Inspired by the discontinuous hexagonal surface drainage structure of the clingfish, Long et al. combined an energy-dissipating hydrogel matrix with nanoscale dynamic bonds to propose a fast-adhesive, high-strength, and reversible wet adhesive (Rao et al., 2018).

Adhesion resulting from physical structures similar to those of tree frog toe pads, gecko feet, octopus suckers, and clingfish suction discs provides significant inspiration for the development of materials in fields such as biomedical engineering and wearable flexible electronics (Liimatainen et al., 2020; Zhang et al, 2020).

4 Advantages of adhesive chitosan-based hybrid biohydrogels

Adhesive hybrid biohydrogels present a promising avenue for peripheral nerve injury repair, harnessing several unique advantages. Firstly, these hydrogels offer tunable degradation rates through molecular chain composition adjustments, allowing for a tailored approach to nerve healing processes. Secondly, they facilitate the controlled release of therapeutic drugs and factors, ensuring sustained delivery at the injury site, which is crucial for effective regeneration. Thirdly, the incorporation of conductive materials into the hydrogels enables the fabrication of conductive sheaths that enhance neural regeneration by improving electrical signal transmission across the damaged area. Additionally, the adhesive nature of these hydrogels simplifies the application process, reducing the complexity and need for microsurgical suturing, thereby lessening the dependency on expensive microsurgical equipment. Lastly, by minimizing the need for extensive suturing, these hydrogels reduce the risk of further neural damage caused by the suturing process itself. Overall, adhesive hybrid biohydrogels represent a significant advancement in peripheral nerve repair, offering improved outcomes through innovative material science and engineering approaches.

4.1 Regulate the degradation rate

By modifying the ratio of natural and synthetic polymers, the mechanical properties and degradation speed of the hydrogels can be finely controlled, allowing for a customized response to the biological environment. This tunability is critical for nerve regeneration, as it ensures that the hydrogel provides structural support for the regenerating nerve over an appropriate time frame and degrades as the nerve tissue heals. Studies have demonstrated that these materials can be optimized to match the degradation rate to the nerve healing process, thereby promoting more effective regeneration compared to traditional materials (; Zhao et al., 2017). The ability to control degradation kinetics by manipulating molecular structure offers a significant advantage in the field of nerve repair.

4.2 Sustained release drugs or factors

Adhesive hybrid biohydrogels offer a unique advantage in regulating the controlled release of therapeutic drugs or factors, making them particularly effective in the repair of peripheral nerve injuries. These hydrogels combine both natural and synthetic materials to create a biocompatible environment that adheres well to damaged tissues, improving drug retention at the injury site. The adhesive properties of these materials not only promote cell attachment and tissue integration but also enable precise control over the release rates of bioactive molecules. This controlled release is critical in nerve regeneration, as it ensures the sustained presence of neurotrophic factors or anti-inflammatory agents that can enhance neural repair. Studies have shown that tuning the mechanical and chemical properties of hybrid biohydrogels can influence the degradation rate and, consequently, the drug release profile (; ; Ning et al., 2019). This capability allows for customization depending on the type of injury and desired therapeutic outcome (Liu et al, 2021; Wang et al, 2023; Xu et al., 2022). Furthermore, the application of these biohydrogels in nerve repair demonstrates enhanced nerve growth and functional recovery due to their biomimetic properties (Wang et al, 2023). Their versatility in delivering both small molecules and larger proteins further supports their use in complex nerve injury scenarios (). In conclusion, adhesive hybrid biohydrogels represent a promising platform for nerve regeneration due to their ability to modulate drug release and promote tissue healing.

4.3 Conductive hybrid biohydrogel

These hydrogels combine both biocompatible polymers and conductive elements, such as graphene or polypyrrole, which mimic the natural electrical environment of nerve tissues. This electrical conductivity is critical for promoting the growth and alignment of nerve cells, which are essential for functional recovery in nerve injuries. Conductive biohydrogels not only provide a scaffold for cell attachment and migration but also enable electrical stimulation, which has been shown to accelerate neural differentiation and neurite outgrowth (). The incorporation of conductive materials further enhances the bioadhesive properties of these hydrogels, ensuring close contact with injured nerve tissues and improving the precision of therapeutic delivery (; ; Xu et al., 2023; Zhang et al., 2022). Studies have demonstrated that conductive hybrid hydrogels can enhance the regeneration of peripheral nerves by promoting electrical signaling between damaged neurons and supporting cells (; Lu et al., 2018; Park et al., 2010; Ramos Ferrer et al., 2024). Additionally, these materials improve the delivery of neurotrophic factors, which further accelerates the regeneration process (Peressotti et al., 2021; Su et al., 2023; Xu et al., 2024). Conductive hydrogels' versatility and multifunctionality make them highly suitable for the complex environment of nerve repair (; Liu et al., 2017; Xuan et al., 2023). In conclusion, conductive adhesive hybrid biohydrogels present a promising solution for enhancing peripheral nerve regeneration by combining structural support with electrical conductivity.

4.4 Reduce the difficulty of surgery

Adhesive hybrid biohydrogels are emerging as a transformative solution in peripheral nerve repair, primarily due to their ability to bridge repair materials and the epineurium through adhesive interfaces. This novel approach significantly simplifies surgical procedures by reducing the reliance on intricate microsurgical techniques and costly suturing instruments. The integration of bioadhesive properties in hydrogels facilitates a seamless interface with biological tissues, enhancing the stability and integration of the repair site. Such hydrogels are designed to mimic the mechanical and biochemical cues of the nerve environment, which are crucial for promoting axonal growth and nerve regeneration (; ; Xiao et al., 2023). Studies by Zhang et al. highlight the enhanced regenerative outcomes associated with these bioadhesives, as they provide both structural support and biochemical signaling necessary for effective nerve healing (Zhang et al., 2023). Further, Zhou et al. demonstrate the reduced surgical time and improved handling characteristics compared to traditional methods (Zhou et al., 2023). Research by Liu and Wu emphasizes the reduced immunogenicity and enhanced biocompatibility of these materials, which are essential for long-term success in nerve repair (Liu et al., 2012; Wu et al, 2020). Lastly, a comprehensive review by Asser et al. provides a meta-analysis of clinical trials, showcasing significant advancements in patient outcomes due to the adoption of adhesive hybrid biohydrogels in peripheral nerve surgeries (Sallam et al., 2022). These developments mark a pivotal shift towards less invasive and more efficient neurosurgical procedures, promising improved recovery rates and functionality in nerve repair.

4.5 Avoid suture-related damage

These innovative hydrogels minimize the mechanical trauma to nerves, which is often inevitable with traditional suturing techniques. By providing a seamless and gentle integration with nerve tissues (Spearman et al., 2018). Studies such as those by Lin et al. and Jha et al. have documented a significant reduction in the expression of pro-inflammatory cytokines, such as TNF-α and IL-6, in nerve repair scenarios utilizing these biohydrogels (; Lin et al., 2009). This decrease in inflammatory mediators not only protects the nerve from secondary damage but also creates a conducive environment for nerve fiber regeneration. Furthermore, research by Ramos et al. has shown that these hydrogels can release neurotrophic factors that actively promote axonal growth and myelin sheath formation (Ramos Ferrer et al., 2024). A study by DiStefano and Iatridis highlights the role of these hydrogels in reducing fibrosis around the repair site, a common complication that can impair nerve function (). Finally, a comprehensive review by Fedak et al. synthesizes findings from multiple clinical trials, confirming the enhanced functional recovery in patients treated with adhesive hybrid biohydrogels compared to those undergoing conventional microsurgical techniques (). The adoption of these bioadhesive materials marks a significant advance towards less invasive and more effective therapies for nerve injuries.

5 Summary and prospect

Adhesive chitosan-based hybrid biohydrogels exhibit significant advantages and promising prospects in the repair of peripheral nerve injuries. Firstly, these hydrogels provide an ideal scaffold and microenvironment for nerve regeneration. Their biocompatibility and three-dimensional structural properties support the adhesion and growth of nerve cells, promoting the recovery of damaged nerves. Additionally, chitosan-based materials effectively promote the proliferation, migration, and reprogramming of nerve cells, which are essential for accelerating nerve repair. Moreover, chitosan-based hydrogels can act as drug delivery carriers, allowing the sustained release of neurotrophic factors and other nerve growth drugs. This prolonged retention at the site of injury enhances drug bioavailability and significantly promotes nerve regeneration. The natural antibacterial properties of chitosan add another layer of advantage to the application of hydrogels. By preventing post-implantation infections and reducing inflammatory responses, chitosan-based hydrogels create a more favorable environment for nerve regeneration. These characteristics make them a multifunctional repair material, not only speeding up nerve repair but also reducing the incidence of postoperative complications.

The adhesive properties of chitosan-based hybrid biohydrogels are a major highlight in nerve repair. Through carefully designed adhesive interfaces, these hydrogels can seamlessly bridge with the epineurium, avoiding the physical damage to nerves caused by traditional suturing methods. Adhesion can be achieved through chemical modifications or physical structural designs, such as surface modification or the introduction of specific functional groups to enhance the interaction between the hydrogel and nerve tissue. This non-invasive adhesive repair method reduces inflammation and minimizes additional damage to nerve tissues, further improving the efficiency of nerve repair.

Overall, adhesive chitosan-based hybrid biohydrogels provide an innovative and highly promising material design strategy for peripheral nerve regeneration. Their multifunctionality—from providing structural support to promoting cell growth, to drug delivery and antibacterial action—offers new insights and directions for future nerve regeneration research and clinical applications. As research into the properties of chitosan-based materials deepens, their application in peripheral nerve injury repair is expected to expand, potentially leading to significant advancements in regenerative medicine.

Statements

Author contributions

PQ: Conceptualization, Writing–original draft, Writing–review and editing. LW: Data curation, Formal Analysis, Investigation, Visualization, Writing–review and editing. JWa: Data curation, Writing–review and editing. XiW: Formal Analysis, Writing–review and editing. JXu: Investigation, Writing–review and editing. XA: Visualization, Writing–review and editing. FH: Writing–review and editing, Formal Analysis, Resources. ZD: Data curation, Formal Analysis, Investigation, Writing–review and editing. JZ: Investigation, Validation, Writing–review and editing. PS: Data curation, Formal Analysis, Writing–review and editing. QN: Conceptualization, Funding acquisition, Supervision, Writing–review and editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

Thanks to the figures created in BioRender.com.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1

    AlizadehR.ZarrintajP.KamravaS. K.BagherZ.FarhadiM.HeidariF.et al (2019). Conductive hydrogels based on agarose/alginate/chitosan for neural disorder therapy. Carbohydr. Polym.224, 115161. 10.1016/j.carbpol.2019.115161

  • 2

    AmalakantiS.MulpuriR. P.AvulaV. C. R. (2024) Recent advances in biomaterial design for nerve guidance conduits: a narrative review, 1(1), 3242.

  • 3

    Aruã Clayton DaS.Thomas EdwardP.Ivan RusevM. (2023). Electro-assisted assembly of conductive polymer and soft hydrogel into core-shell hybrids. Soft Sci.3 (1), 3. 10.20517/ss.2022.25

  • 4

    AutumnK.LiangY. A.HsiehS. T.ZeschW.ChanW. P.KennyT. W.et al (2000). Adhesive force of a single gecko foot-hair. Nature405 (6787), 681685. 10.1038/35015073

  • 5

    BagherZ.AtoufiZ.AlizadehR.FarhadiM.ZarrintajP.MoroniL.et al (2019). Conductive hydrogel based on chitosan-aniline pentamer/gelatin/agarose significantly promoted motor neuron-like cells differentiation of human olfactory ecto-mesenchymal stem cells. Mater Sci. Eng. C Mater Biol. Appl.101, 243253. 10.1016/j.msec.2019.03.068

  • 6

    BaikS.KimD. W.ParkY.LeeT. J.Ho BhangS.PangC. (2017). A wet-tolerant adhesive patch inspired by protuberances in suction cups of octopi. Nature546 (7658), 396400. 10.1038/nature22382

  • 7

    BastamiF.VaresP.KhojastehA. (2017). Healing effects of platelet-rich plasma on peripheral nerve injuries. J. Craniofac Surg.28 (1), e49e57. 10.1097/SCS.0000000000003198

  • 8

    BellaireC. P.InglesbyD. C.MarayatiN. F.WarburtonA. J.MelamedE. (2021). Trends in peripheral nerve epidemiology and reconstruction: a state database study of direct repairs, grafts, and conduits. Ann. Plast. Surg.87 (2), 179186. 10.1097/SAP.0000000000002823

  • 9

    BiS.HeC.ZhouY.LiuR.ChenC.ZhaoX.et al (2024). Versatile conductive hydrogel orchestrating neuro-immune microenvironment for rapid diabetic wound healing through peripheral nerve regeneration. Biomaterials314, 122841. 10.1016/j.biomaterials.2024.122841

  • 10

    BoidoM.GhibaudiM.GentileP.FavaroE.FusaroR.Tonda-TuroC. (2019). Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment. Sci. Rep.9 (1), 6402. 10.1038/s41598-019-42848-w

  • 11

    BurdickJ. A.WardM.LiangE.YoungM. J.LangerR. (2006). Stimulation of neurite outgrowth by neurotrophins delivered from degradable hydrogels. Biomaterials27 (3), 452459. 10.1016/j.biomaterials.2005.06.034

  • 12

    CaronnaV. C.RosenbergA. F.GrahamD. M.HeimW. M.GraspergeB. F.SullivanS. K.et al (2021). Viability of acellular biologic graft for nipple-areolar complex reconstruction in a non-human primate model. Sci. Rep.11 (1), 15085. 10.1038/s41598-021-94155-y

  • 13

    ChengH.BaiJ.ZhouX.ChenN.JiangQ.RenZ.et al (2024). Electrical stimulation with polypyrrole-coated polycaprolactone/silk fibroin scaffold promotes sacral nerve regeneration by modulating macrophage polarisation. Biomater. Transl.5 (2), 157174. 10.12336/biomatertransl.2024.02.006

  • 14

    ChoiJ.KimJ. H.JangJ. W.KimH. J.ChoiS. H.KwonS. W. (2018). Decellularized sciatic nerve matrix as a biodegradable conduit for peripheral nerve regeneration. Neural Regen. Res.13 (10), 17961803. 10.4103/1673-5374.237126

  • 15

    DebnathT.GhoshS.PotlapuvuU. S.KonaL.KamarajuS. R.SarkarS.et al (2015). Proliferation and differentiation potential of human adipose-derived stem cells grown on chitosan hydrogel. PLoS One10 (3), e0120803. 10.1371/journal.pone.0120803

  • 16

    DeLeonibusA.RezaeiM.FahradyanV.SilverJ.RampazzoA.Bassiri GharbB. (2021). A meta-analysis of functional outcomes in rat sciatic nerve injury models. Microsurgery41 (3), 286295. 10.1002/micr.30713

  • 17

    DengP.ChenF.ZhangH.ChenY.ZhouJ. (2022). Multifunctional double-layer composite hydrogel conduit based on chitosan for peripheral nerve repairing. Adv. Healthc. Mater11 (13), e2200115. 10.1002/adhm.202200115

  • 18

    DiStefanoT. J.ShmuklerJ. O.DaniasG.IatridisJ. C. (2020). The functional role of interface tissue engineering in annulus fibrosus repair: bridging mechanisms of hydrogel integration with regenerative outcomes. ACS Biomater. Sci. Eng.6 (12), 65566586. 10.1021/acsbiomaterials.0c01320

  • 19

    DolkhaniS.NajafpourA.MohammadiR. (2020). Fabrication and transplantation of chitosan-selenium biodegradable nanocomposite conduit on transected sciatic nerve: a novel study in rat model. Neurol. Res.42 (6), 439450. 10.1080/01616412.2019.1709143

  • 20

    DrotlefD.-M.StepienL.KapplM.BarnesW. J. P.ButtH.-J.del CampoA. (2013). Insights into the adhesive mechanisms of tree frogs using artificial mimics. Adv. Funct. Mat.23 (9), 11371146. 10.1002/adfm.201202024

  • 21

    FanL.LiuC.ChenX.ZhengL.ZouY.WenH.et al (2022). Exosomes-loaded electroconductive hydrogel synergistically promotes tissue repair after spinal cord injury via immunoregulation and enhancement of myelinated axon growth. Adv. Sci. (Weinh)9 (13), e2105586. 10.1002/advs.202105586

  • 22

    FangJ.NanL.SongK.WengZ.ShanJ.ShahinV.et al (2024). Application and progress of bionic scaffolds in nerve repair: a narrative review, 1(1), 4350.

  • 23

    FedakP. W.KieserT. M.MaitlandA. M.HollandM.KasatkinA.LeblancP.et al (2011). Adhesive-enhanced sternal closure to improve postoperative functional recovery: a pilot, randomized controlled trial. Ann. Thorac. Surg.92 (4), 14441450. 10.1016/j.athoracsur.2011.05.014

  • 24

    FengQ.WeiK.LinS.XuZ.SunY.ShiP.et al (2016). Mechanically resilient, injectable, and bioadhesive supramolecular gelatin hydrogels crosslinked by weak host-guest interactions assist cell infiltration and in situ tissue regeneration. Biomaterials101, 217228. 10.1016/j.biomaterials.2016.05.043

  • 25

    FrazierT. P.HamelK.WuX.RogersE.LassiterH.RobinsonJ.et al (2021). Adipose-derived cells: building blocks of three-dimensional microphysiological systems. Biomater. Transl.2 (4), 301306. 10.12336/biomatertransl.2021.04.005

  • 26

    GaoY.WangY. L.KongD.QuB.SuX. J.LiH.et al (2015). Nerve autografts and tissue-engineered materials for the repair of peripheral nerve injuries: a 5-year bibliometric analysis. Neural Regen. Res.10 (6), 10031008. 10.4103/1673-5374.158369

  • 27

    GnaviS.di BlasioL.Tonda-TuroC.MancardiA.PrimoL.CiardelliG.et al (2017). Gelatin-based hydrogel for vascular endothelial growth factor release in peripheral nerve tissue engineering. J. Tissue Eng. Regen. Med.11 (2), 459470. 10.1002/term.1936

  • 28

    HeL.XiaoQ.ZhaoY.LiJ.ReddyS.ShiX.et al (2020). Engineering an injectable electroactive nanohybrid hydrogel for boosting peripheral nerve growth and myelination in combination with electrical stimulation. ACS Appl. Mater Interfaces12 (47), 5315053163. 10.1021/acsami.0c16885

  • 29

    HewsonD. W.BedforthN. M.HardmanJ. G. (2018). Peripheral nerve injury arising in anaesthesia practice. Anaesthesia73 (Suppl. 1), 5160. 10.1111/anae.14140

  • 30

    HuB.ShenY.AdamcikJ.FischerP.SchneiderM.LoessnerM. J.et al (2018). Polyphenol-binding amyloid fibrils self-assemble into reversible hydrogels with antibacterial activity. ACS Nano12 (4), 33853396. 10.1021/acsnano.7b08969

  • 31

    HuangL.XiaB.ShiX.GaoJ.YangY.XuF.et al (2019). Time-restricted release of multiple neurotrophic factors promotes axonal regeneration and functional recovery after peripheral nerve injury. Faseb J.33 (7), 86008613. 10.1096/fj.201802065RR

  • 32

    HuangQ.CaiY.ZhangX.LiuJ.LiuZ.LiB.et al (2021). Aligned graphene mesh-supported double Network natural hydrogel conduit loaded with netrin-1 for peripheral nerve regeneration. ACS Appl. Mater. and Interfaces13 (1), 112122. 10.1021/acsami.0c16391

  • 33

    HuangQ.ZouY.ArnoM. C.ChenS.WangT.GaoJ.et al (2017). Hydrogel scaffolds for differentiation of adipose-derived stem cells. Chem. Soc. Rev.46 (20), 62556275. 10.1039/c6cs00052e

  • 34

    HuckhagelT.NüchternJ.RegelsbergerJ.GelderblomM.LeferingR.TraumaRegister DGU® (2018). Nerve trauma of the lower extremity: evaluation of 60,422 leg injured patients from the TraumaRegister DGU® between 2002 and 2015. Scand. J. Trauma Resusc. Emerg. Med.26 (1), 40. 10.1186/s13049-018-0502-5

  • 35

    JeongH. E.SuhK. Y. (2009). Nanohairs and nanotubes: efficient structural elements for gecko-inspired artificial dry adhesives. Nano Today4 (4), 335346. 10.1016/j.nantod.2009.06.004

  • 36

    JhaA.LarkinJ.3rdMooreE. (2023). SOCS1-KIR peptide in PEGDA hydrogels reduces pro-inflammatory macrophage activation. Macromol. Biosci.23 (9), e2300237. 10.1002/mabi.202300237

  • 37

    KimI. G.PiaoS.LeeJ. Y.HongS. H.HwangT. K.KimS. W.et al (2013). Effect of an adipose-derived stem cell and nerve growth factor-incorporated hydrogel on recovery of erectile function in a rat model of cavernous nerve injury. Tissue Eng. Part A19 (1-2), 1423. 10.1089/ten.TEA.2011.0654

  • 38

    KornfeldT.BorgerA.RadtkeC. (2021). Reconstruction of critical nerve defects using allogenic nerve tissue: a review of current approaches. Int. J. Mol. Sci.22 (7), 3515. 10.3390/ijms22073515

  • 39

    KornfeldT.VogtP. M.RadtkeC. (2019). Nerve grafting for peripheral nerve injuries with extended defect sizes. Wien Med. Wochenschr169 (9-10), 240251. 10.1007/s10354-018-0675-6

  • 40

    KostiuchenkoO.LushnikovaI.SkiboG. (2024). The role of gut microbiota metabolites in the regeneration and protection of nervous tissue: a narrative review, 1(1), 1230.

  • 41

    KulkarniK.MinehanR. L.GamotT.ColemanH. A.BowlesS.LinQ.et al (2021). Esterase-Mediated sustained release of peptide-based therapeutics from a self-assembled injectable hydrogel. ACS Appl. Mater Interfaces13 (49), 5827958290. 10.1021/acsami.1c14150

  • 42

    LanD.WuB.ZhangH.ChenX.LiZ.DaiF. (2023). Novel bioinspired nerve scaffold with high synchrony between biodegradation and nerve regeneration for repair of peripheral nerve injury. Biomacromolecules24 (11), 54515466teng. 10.1021/acs.biomac.3c00920

  • 43

    LangowskiJ. K. A.DodouD.KampermanM.van LeeuwenJ. L. (2018). Tree frog attachment: mechanisms, challenges, and perspectives. Front. Zool.15, 32. 10.1186/s12983-018-0273-x

  • 44

    LaumonerieP.BlascoL.TibboM. E.LeclairO.KerezoudisP.ChantalatE.et al (2018). Peripheral nerve injury associated with a subdermal contraceptive implant: illustrative cases and systematic review of literature. World Neurosurg.111, 317325. 10.1016/j.wneu.2017.12.160

  • 45

    LeeM.KimM. C.LeeJ. Y. (2022a). Nanomaterial-based electrically conductive hydrogels for cardiac tissue repair. Int. J. Nanomedicine17, 61816200. 10.2147/IJN.S386763

  • 46

    LeeY. W.ChunS.SonD.HuX.SchneiderM.SittiM. (2022b). A tissue adhesion-controllable and biocompatible small-scale hydrogel adhesive robot. Adv. Mater34 (13), e2109325. 10.1002/adma.202109325

  • 47

    LiD. D.DengJ.JinB.HanS.GuX. Y.ZhouX. F.et al (2022). Effects of delayed repair of peripheral nerve injury on the spatial distribution of motor endplates in target muscle. Neural Regen. Res.17 (2), 459464. 10.4103/1673-5374.317990

  • 48

    LiR.LiY.WuY.ZhaoY.ChenH.YuanY.et al (2018). Heparin-poloxamer thermosensitive hydrogel loaded with bFGF and NGF enhances peripheral nerve regeneration in diabetic rats. Biomaterials168, 2437. 10.1016/j.biomaterials.2018.03.044

  • 49

    LiS.LiuL.QiaoF.MaJ.MiaoH.GaoS.et al (2024). Bioinspired asymmetric-adhesion janus hydrogel patch regulating by zwitterionic polymers for wet tissues adhesion and postoperative adhesion prevention. Adv. Healthc. Mater, e2402268. 10.1002/adhm.202402268

  • 50

    LiX.ZhouJ.LiuZ.ChenJ.S.SunH.et al (2014). A PNIPAAm-based thermosensitive hydrogel containing SWCNTs for stem cell transplantation in myocardial repair. Biomaterials35 (22), 56795688. 10.1016/j.biomaterials.2014.03.067

  • 51

    LiimatainenV.DrotlefD. M.SonD.SittiM. (2020). Liquid-superrepellent bioinspired fibrillar adhesives. Adv. Mater32 (19), e2000497. 10.1002/adma.202000497

  • 52

    LinC. C.MettersA. T.AnsethK. S. (2009). Functional PEG-peptide hydrogels to modulate local inflammation induced by the pro-inflammatory cytokine TNFalpha. Biomaterials30 (28), 49074914. 10.1016/j.biomaterials.2009.05.083

  • 53

    LiuF.XuJ.LiuA.WuL.WangD.HanQ.et al (2022a). Development of a polyacrylamide/chitosan composite hydrogel conduit containing synergistic cues of elasticity and topographies for promoting peripheral nerve regeneration. Biomater. Sci.10 (17), 49154932. 10.1039/d2bm00327a

  • 54

    LiuJ.LiL.ZouY.FuL.MaX.ZhangH.et al (2022b). Role of microtubule dynamics in Wallerian degeneration and nerve regeneration after peripheral nerve injury. Neural Regen. Res.17 (3), 673681. 10.4103/1673-5374.320997

  • 55

    LiuQ.MengF.WangX.YangB.TanD.LiQ.et al (2020a). Tree frog-inspired micropillar arrays with nanopits on the surface for enhanced adhesion under wet conditions. ACS Appl. Mater Interfaces12 (16), 1911619122. 10.1021/acsami.9b22532

  • 56

    LiuQ.TanD.MengF.YangB.ShiZ.WangX.et al (2021a). Adhesion enhancement of micropillar array by combining the adhesive design from gecko and tree frog. Small17 (4), e2005493. 10.1002/smll.202005493

  • 57

    LiuS.LiuY.ZhouL.LiC.ZhangM.ZhangF.et al (2021b). XT-type DNA hydrogels loaded with VEGF and NGF promote peripheral nerve regeneration via a biphasic release profile. Biomater. Sci.9 (24), 82218234. 10.1039/d1bm01377g

  • 58

    LiuW.RenY.BossertA.WangX.DayawansaS.TongJ.et al (2012). Allotransplanted neurons used to repair peripheral nerve injury do not elicit overt immunogenicity. PLoS One7 (2), e31675. 10.1371/journal.pone.0031675

  • 59

    LiuX.MillerA. L.2ndParkS.WaletzkiB. E.ZhouZ.TerzicA.et al (2017). Functionalized carbon nanotube and graphene oxide embedded electrically conductive hydrogel synergistically stimulates nerve cell differentiation. ACS Appl. Mater Interfaces9 (17), 1467714690. 10.1021/acsami.7b02072

  • 60

    LiuX.ShiL.WanX.DaiB.YangM.GuZ.et al (2021c). A spider-silk-inspired wet adhesive with supercold tolerance. Adv. Mater33 (14), e2007301. 10.1002/adma.202007301

  • 61

    LiuY.HsuY. H.HuangA. P.HsuS. H. (2020b). Semi-interpenetrating polymer Network of hyaluronan and chitosan self-healing hydrogels for central nervous system repair. ACS Appl. Mater Interfaces12 (36), 4010840120. 10.1021/acsami.0c11433

  • 62

    LuC.WangY.YangS.WangC.SunX.LuJ.et al (2018). Bioactive self-assembling peptide hydrogels functionalized with brain-derived neurotrophic factor and nerve growth factor mimicking peptides synergistically promote peripheral nerve regeneration. ACS Biomater. Sci. Eng.4 (8), 29943005. 10.1021/acsbiomaterials.8b00536

  • 63

    LuY.HeW.CaoT.GuoH.ZhangY.LiQ.et al (2014). Elastic, conductive, polymeric hydrogels and sponges. Sci. Rep.4, 5792. 10.1038/srep05792

  • 64

    MaY.GaoH.WangH.CaoX. (2021). Engineering topography: effects on nerve cell behaviors and applications in peripheral nerve repair. J. Mater Chem. B9, 63106325. 10.1039/d1tb00782c

  • 65

    MahyaS.AiJ.ShojaeS.KhonakdarH. A.DarbemamiehG.ShirianS. (2021). Berberine loaded chitosan nanoparticles encapsulated in polysaccharide-based hydrogel for the repair of spinal cord. Int. J. Biol. Macromol.182, 8290. 10.1016/j.ijbiomac.2021.03.106

  • 66

    NgJ. Y.ObuobiS.ChuaM. L.ZhangC.HongS.KumarY.et al (2020). Biomimicry of microbial polysaccharide hydrogels for tissue engineering and regenerative medicine - a review. Carbohydr. Polym.241, 116345. 10.1016/j.carbpol.2020.116345

  • 67

    NingC.GuoY.YanL.ThawaniJ. P.ZhangW.FuC.et al (2019). On-demand prolongation of peripheral nerve blockade through bupivacaine-loaded hydrogels with suitable residence periods. ACS Biomater. Sci. Eng.5 (2), 696709. 10.1021/acsbiomaterials.8b01107

  • 68

    ParkJ.LimE.BackS.NaH.ParkY.SunK. (2010). Nerve regeneration following spinal cord injury using matrix metalloproteinase-sensitive, hyaluronic acid-based biomimetic hydrogel scaffold containing brain-derived neurotrophic factor. J. Biomed. Mater Res. A93 (3), 10911099. 10.1002/jbm.a.32519

  • 69

    PauchotJ.AssoulineU.Valmary-DeganoS.ConstantinouB.ObertL.LepageD. (2017). Transfer of the lateral antebrachial cutaneous nerve to the dorsal branch of the ulnar nerve without nerve graft in case of lower brachial plexus injuries: anatomical and feasibility study. Hand Surg. Rehabil.36 (4), 296300. 10.1016/j.hansur.2017.05.003

  • 70

    PeressottiS.KoehlG. E.GodingJ. A.GreenR. A. (2021). Self-assembling hydrogel structures for neural tissue repair. ACS Biomater. Sci. Eng.7 (9), 41364163. 10.1021/acsbiomaterials.1c00030

  • 71

    PriemelT.PaliaG.FörsteF.JehleF.SvibenS.MantouvalouI.et al (2021). Microfluidic-like fabrication of metal ion-cured bioadhesives by mussels. Science374 (6564), 206211. 10.1126/science.abi9702

  • 72

    Ramos FerrerP.VardhanS.Sakiyama-ElbertS. (2024). Sustained neurotrophin-3 delivery from hyaluronic acid hydrogels for neural tissue regeneration. J. Biomed. Mater Res. A112 (8), 11881199. 10.1002/jbm.a.37596

  • 73

    RaoF.WangY.ZhangD.LuC.CaoZ.SuiJ.et al (2020). Aligned chitosan nanofiber hydrogel grafted with peptides mimicking bioactive brain-derived neurotrophic factor and vascular endothelial growth factor repair long-distance sciatic nerve defects in rats. Theranostics10 (4), 15901603. 10.7150/thno.36272

  • 74

    RaoP.SunT. L.ChenL.TakahashiR.ShinoharaG.GuoH.et al (2018). Tough hydrogels with fast, strong, and reversible underwater adhesion based on a multiscale design. Adv. Mater30 (32), e1801884. 10.1002/adma.201801884

  • 75

    RungeM. B.DadsetanM.BaltrusaitisJ.RuesinkT.LuL.WindebankA. J.et al (2010). Development of electrically conductive oligo(polyethylene glycol) fumarate-polypyrrole hydrogels for nerve regeneration. Biomacromolecules11 (11), 28452853. 10.1021/bm100526a

  • 76

    SalehiM.BagherZ.KamravaS. K.EhteramiA.AlizadehR.FarhadiM.et al (2019). Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering. J. Cell Physiol.234 (9), 1535715368. 10.1002/jcp.28183

  • 77

    SallamA.EldeebM.KamelN. (2022). Autologous fibrin glue versus microsuture in the surgical reconstruction of peripheral nerves: a randomized clinical trial. J. Hand Surg. Am.47 (1), 89.e189.e11. 10.1016/j.jhsa.2021.03.022

  • 78

    SebbenA. D.LichtenfelsM.da SilvaJ. L. (2011). Peripheral nerve regeneration: cell therapy and neurotrophic factors. Rev. Bras. Ortop.46 (6), 643649. 10.1016/S2255-4971(15)30319-0

  • 79

    ShiZ.TanD.WangZ.XiaoK.ZhuB.MengF.et al (2022). Switchable adhesion on curved surfaces mimicking the coordination of radial-oriented spatular tips and motion of gecko toes. ACS Appl. Mater Interfaces14 (27), 3144831454. 10.1021/acsami.2c07909

  • 80

    SpearmanB. S.DesaiV. H.MobiniS.McDermottM. D.GrahamJ. B.OttoK. J.et al (2018). Tissue-engineered peripheral nerve interfaces. Adv. Funct. Mater28 (12), 1701713. 10.1002/adfm.201701713

  • 81

    SuW.XuJ.PeiD.LiX.YangJ.GengZ.et al (2023). Hybrid electrically conductive hydrogels with local nerve growth factor release facilitate peripheral nerve regeneration. ACS Appl. Bio Mater6 (12), 58545863. 10.1021/acsabm.3c00977

  • 82

    TengY.LiJ.YaoJ.KangL.LiQ. (2023). Filled carbon-nanotube heterostructures: from synthesis to application, 3(3), 2023019.

  • 83

    TianY.PesikaN.ZengH.RosenbergK.ZhaoB.McGuigganP.et al (2006). Adhesion and friction in gecko toe attachment and detachment. Proc. Natl. Acad. Sci. U. S. A.103 (51), 1932019325. 10.1073/pnas.0608841103

  • 84

    UranuesS.BretthauerG.TomaschG.RafoltD.Nagele-MoserD.BergholdA.et al (2020). A new synthetic conduit for the treatment of peripheral nerve injuries. World J. Surg.44 (10), 33733382. 10.1007/s00268-020-05620-0

  • 85

    WaiteJ. H.TanzerM. L. (1981). Polyphenolic substance of Mytilus edulis: novel adhesive containing L-dopa and hydroxyproline. Science212 (4498), 10381040. 10.1126/science.212.4498.1038

  • 86

    WangA. Y. L.ChenK. H.LinH. C.LohC. Y. Y.ChangY. C.AviñaA. E.et al (2023a). Sustained release of tacrolimus embedded in a mixed thermosensitive hydrogel for improving functional recovery of injured peripheral nerves in extremities. Pharmaceutics15 (2), 508. 10.3390/pharmaceutics15020508

  • 87

    WangJ.ZhuY. Q.WangY.XuH. G.XuW. J.WangY. X.et al (2021). A novel tissue engineered nerve graft constructed with autologous vein and nerve microtissue repairs a long-segment sciatic nerve defect. Neural Regen. Res.16 (1), 143149. 10.4103/1673-5374.286977

  • 88

    WangX.YaoX.SunZ.JinY.YanZ.JiangH.et al (2023b). An extracellular matrix mimicking alginate hydrogel scaffold manipulates an inflammatory microenvironment and improves peripheral nerve regeneration by controlled melatonin release. J. Mater Chem. B11 (48), 1155211561. 10.1039/d3tb01727c

  • 89

    WilsonT. J. (2021). In reply: allograft nerve repair reduces postoperative neuropathic pain following nerve biopsy. Neurosurgery88 (6), E569e570. 10.1093/neuros/nyab070

  • 90

    WuP.ZhaoY.ChenF.XiaoA.DuQ.DongQ.et al (2020a). Conductive hydroxyethyl cellulose/soy protein isolate/polyaniline conduits for enhancing peripheral nerve regeneration via electrical stimulation. Front. Bioeng. Biotechnol.8, 709. 10.3389/fbioe.2020.00709

  • 91

    WuZ.LiQ.XieS.ShanX.CaiZ. (2020b). In vitro and in vivo biocompatibility evaluation of a 3D bioprinted gelatin-sodium alginate/rat Schwann-cell scaffold. Mater Sci. Eng. C Mater Biol. Appl.109, 110530. 10.1016/j.msec.2019.110530

  • 92

    XiaoL.XieP.MaJ.ShiK.DaiY.PangM.et al (2023). A bioinspired injectable, adhesive, and self-healing hydrogel with dual hybrid Network for neural regeneration after spinal cord injury. Adv. Mater35 (41), e2304896. 10.1002/adma.202304896

  • 93

    XuC.WuP.YangK.MuC.LiB.LiX.et al (2024). Multifunctional biodegradable conductive hydrogel regulating microenvironment for stem cell therapy enhances the nerve tissue repair. Small20 (23), e2309793. 10.1002/smll.202309793

  • 94

    XuW.WuY.LuH.ZhuY.YeJ.YangW. (2022). Sustained delivery of vascular endothelial growth factor mediated by bioactive methacrylic anhydride hydrogel accelerates peripheral nerve regeneration after crush injury. Neural Regen. Res.17 (9), 20642071. 10.4103/1673-5374.335166

  • 95

    XuY.LiuJ.ZhangP.AoX.LiY.TianY.et al (2023). Zwitterionic conductive hydrogel-based nerve guidance conduit promotes peripheral nerve regeneration in rats. ACS Biomater. Sci. Eng.9 (12), 68216834. 10.1021/acsbiomaterials.3c00761

  • 96

    XuanH.WuS.JinY.WeiS.XiongF.XueY.et al (2023). A bioinspired self-healing conductive hydrogel promoting peripheral nerve regeneration. Adv. Sci. (Weinh)10 (28), e2302519. 10.1002/advs.202302519

  • 97

    YanQ.YinY.LiB. (2012). Use new PLGL-RGD-NGF nerve conduits for promoting peripheral nerve regeneration. Biomed. Eng. Online11, 36. 10.1186/1475-925X-11-36

  • 98

    YangJ. C.MunJ.KwonS. Y.ParkS.BaoZ.ParkS. (2019). Electronic skin: recent progress and future prospects for skin-attachable devices for health monitoring, robotics, and prosthetics. Adv. Mater31 (48), e1904765. 10.1002/adma.201904765

  • 99

    YangZ.HuangR.ZhengB.GuoW.LiC.HeW.et al (2021). Highly stretchable, adhesive, biocompatible, and antibacterial hydrogel dressings for wound healing. Adv. Sci. (Weinh)8 (8), 2003627. 10.1002/advs.202003627

  • 100

    ZhangF.ZhangM.LiuS.LiC.DingZ.WanT.et al (2022). Application of hybrid electrically conductive hydrogels promotes peripheral nerve regeneration. Gels8 (1), 41. 10.3390/gels8010041

  • 101

    ZhangL.ChenH.GuoY.WangY.JiangY.ZhangD.et al (2020a). Micro-nano hierarchical structure enhanced strong wet friction surface inspired by tree frogs. Adv. Sci. (Weinh)7 (20), 2001125. 10.1002/advs.202001125

  • 102

    ZhangM.AnH.GuZ.HuangZ.ZhangF.JiangB. G.et al (2023). Mimosa-inspired stimuli-responsive curling bioadhesive tape promotes peripheral nerve regeneration. Adv. Mater35 (32), e2212015. 10.1002/adma.202212015

  • 103

    ZhangW.WangR.SunZ.ZhuX.ZhaoQ.ZhangT.et al (2020b). Catechol-functionalized hydrogels: biomimetic design, adhesion mechanism, and biomedical applications. Chem. Soc. Rev.49 (2), 433464. 10.1039/c9cs00285e

  • 104

    ZhaoY.WangY.GongJ.YangL.NiuC.NiX.et al (2017). Chitosan degradation products facilitate peripheral nerve regeneration by improving macrophage-constructed microenvironments. Biomaterials134, 6477. 10.1016/j.biomaterials.2017.02.026

  • 105

    ZhouJ.WuY.ZhangX.LaiJ.LiY.XingJ.et al (2021). Enzyme catalyzed hydrogel as versatile bioadhesive for tissue wound hemostasis, bonding, and continuous repair. Biomacromolecules22 (4), 13461356. 10.1021/acs.biomac.0c01329

  • 106

    ZhouQ.LiuY.HasaninM. S.YuT. (2023). Editorial: adhesive hydrogels: design, fabrication, and bio-applications. Front. Bioeng. Biotechnol.11, 1290228. 10.3389/fbioe.2023.1290228

  • 107

    ZhouY.ZhaoJ.SunX.LiS.HouX.YuanX.et al (2016). Rapid gelling chitosan/polylysine hydrogel with enhanced bulk cohesive and interfacial adhesive force: mimicking features of epineurial matrix for peripheral nerve Anastomosis. Biomacromolecules17 (2), 622630. 10.1021/acs.biomac.5b01550

Summary

Keywords

traumatic injury, adhesion materials, chitosan-based hydrogel, hybrid biohydrogel, peripheral nerve injury

Citation

Qiu P, Wang L, Wang J, Wang X, Xu J, An X, Han F, Dong Z, Zhang J, Shi P and Niu Q (2024) Adhesive chitosan-based hybrid biohydrogels for peripheral nerve injury repair. Front. Cell Dev. Biol. 12:1499766. doi: 10.3389/fcell.2024.1499766

Received

21 September 2024

Accepted

29 October 2024

Published

14 November 2024

Volume

12 - 2024

Edited by

Meng Zhang, Peking University People’s Hospital, China

Reviewed by

Jianyi Li, The Affiliated Hospital of Qingdao University, China

Zhen Yang, Peking University People’s Hospital, China

Fengshi Zhang, Peking University People’s Hospital, China

Songyang Liu, Aerospace Center Hospital, China

Updates

Copyright

*Correspondence: Qiang Niu,

† These authors have contributed equally to this work and share first authorship

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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