Microenvironment-Modulating Hyaluronic Acid-Tannic Acid Hydrogel for Peripheral Nerve Injury Repair.

IF 9.6
Yao Liu, Kai Liu, Yu Yan, Xiaonong Zhang, Chunsheng Xiao, Zhiming Song, Bin Liu
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Abstract

Peripheral nerve injury typically results in the loss of nervous tissues and motor and sensory functions, leading to serious clinical complications. Excessive oxidative stress and inflammations in the damaged area can severely inhibit nerve regeneration, making the repair of damaged nerve tissues challenging. In this study, we developed a microenvironment-modulating hyaluronic acid-based hydrogel crosslinked with tannic acid (HPTA) and evaluated its effectiveness in treating peripheral nerve injury. The prepared hydrogel demonstrates good injectability, antioxidative and anti-inflammatory properties, and good biocompatibility. By modulating the microenvironmental oxidative stress and reducing inflammation in damaged areas, the HPTA hydrogel effectively improved the motor function in rats with sciatic nerve crush injury, significantly reduced muscular atrophy, protected neuronal, and enhanced nerve regeneration and remyelination. Additionally, the HPTA@MeCbl hydrogel, loaded with a therapeutic agent methylcobalamin (MeCbl), showed enhanced treatment of damaged nerves through gradually releasing MeCbl at the injury site. Animal studies demonstrated that HPTA@MeCbl hydrogel significantly promotes functional recovery and axonal regeneration in the lower limbs after sciatic nerve transection. In conclusion, the microenvironment-modulating HPTA hydrogel developed in this study offers a promising strategy for developing high-performance biomaterials for nerve repair. STATEMENT OF SIGNIFICANCE: Peripheral nerve injury remains a major clinical challenge due to limited regenerative capacity and the hostile microenvironment characterized by oxidative stress and inflammation. This study presents a hyaluronic acid-based hydrogel crosslinked with tannic acid (HPTA) that actively modulates the injury microenvironment by attenuating oxidative stress and inflammation, thereby facilitating nerve regeneration. Furthermore, incorporating methylcobalamin (MeCbl) into the hydrogel (HPTA@MeCbl) enables localized and sustained drug release, significantly enhancing axonal regrowth and functional recovery in both crush and transection nerve injury models. This work introduces a clinically translatable, microenvironment-modulating hydrogel platform with dual therapeutic functionalities, offering a promising strategy for advanced peripheral nerve repair.

微环境调节透明质酸-单宁酸水凝胶用于周围神经损伤修复。
周围神经损伤通常导致神经组织、运动和感觉功能的丧失,导致严重的临床并发症。受损区域过度的氧化应激和炎症会严重抑制神经再生,使受损神经组织的修复变得困难。在这项研究中,我们开发了一种微环境调节透明质酸-单宁酸交联水凝胶(HPTA),并评估了其治疗周围神经损伤的有效性。所制备的水凝胶具有良好的注射性、抗氧化和抗炎性能以及良好的生物相容性。HPTA水凝胶通过调节微环境氧化应激,减轻损伤区炎症反应,有效改善坐骨神经挤压损伤大鼠运动功能,显著减少肌肉萎缩,保护神经元,促进神经再生和髓鞘再生。此外,HPTA@MeCbl水凝胶加载治疗药物甲基钴胺素(MeCbl),通过在损伤部位逐渐释放MeCbl,显示出对受损神经的增强治疗作用。动物实验表明,HPTA@MeCbl水凝胶可显著促进坐骨神经断裂后下肢功能恢复和轴突再生。综上所述,本研究开发的微环境调节HPTA水凝胶为开发高性能神经修复生物材料提供了一种很有前景的策略。意义声明:由于再生能力有限以及以氧化应激和炎症为特征的恶劣微环境,周围神经损伤仍然是一个主要的临床挑战。本研究提出了一种以透明质酸为基础的单宁酸交联水凝胶(HPTA),通过减轻氧化应激和炎症,积极调节损伤微环境,从而促进神经再生。此外,在水凝胶中加入甲基钴胺素(MeCbl) (HPTA@MeCbl)可以实现局部和持续的药物释放,显著增强挤压和横断神经损伤模型中的轴突再生和功能恢复。这项工作介绍了一种具有双重治疗功能的临床可翻译的微环境调节水凝胶平台,为高级周围神经修复提供了一种有前途的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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