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
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 (
FIGURE 3

(A) Hydrogel tissue-engineered nerve conduits loaded with growth factors. (Figures reproduced from Su et al., 2023). Reprinted (adapted) with permission from {ACS Applied Bio Materials}. Copyright {2023} American Chemical Society. (B) Hydrogel tissue-engineered nerve conduits loaded with stem cells. hADSCs cultured on chitosan hydrogel on different days, the arrows in bright field image shows actively growing stem cells present in the hydrogel (Figures reproduced from
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 (
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 (
FIGURE 4

Biohydrogel adhesion based on catechols groups. (A) Formation of Hydrogel Network; (B) Gelation Mechanism through Michael Addition; (C) Schematic of Nerve Anastomosis Test; (D) Schematic of Interactions inside the Adhesives (Figures reproduced from Zhou et al., 2016).
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 (
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) (
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) (
FIGURE 5

Physical structure adhesion in nature. (A1) Forelimbs of Litoria caerulea. (A2) Schematic lateral view of tendons, phalangi (dark grey), and the intercalary element (light grey) in a digit of Scinax squalirostris. (A3) Schematic depiction of the collagen fibres in a pad of Hyla dominicensis in dorsal view. B Superficial and internal pad structures in L. caerulea. (B1) SEM image of the ventral epidermis. (B2) Transverse section through the toe of a juvenile frog. C Epidermal cells on the ventral surface. (C1) SEM image of polygonal cells in L. caerulea. (C2) TEM image of a tangential cross-section through the apical part of two adjacent cells in Hyla cinerea. D Fine structures of the apical surface of an epidermal cell. (D1) High power SEM image of nanopillars and their central depressions (“dimples”) in L. caerulea. (D2) TEM image of a cross-section through a row of nanopillars in H. cinerea (black arrows: EDM). BV blood vessels, CFG circumferential groove, CH channel between two epidermal cells/nanopillars, CO collagen fibres, D dermis, DE dorsal epidermis, DI dimple, EC epidermal cell, EDM electron dense material, ET extensor brevis profundus tendon, I.E., intercalary element, MG mucus gland, MP mucus pore, NP nanopillar, PC pad curvature, PH (terminal) phalanx, TO tonofilaments, TS tendo superficialis, VE ventral epidermis. The illustrations are not to scale (Figures reproduced from
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 (
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 (
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 (
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 (
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 (
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.
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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
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© 2024 Qiu, Wang, Wang, Wang, Xu, An, Han, Dong, Zhang, Shi and Niu.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Qiang Niu, niuqguke@sina.com
† These authors have contributed equally to this work and share first authorship
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