Paravertebrally-Injected Multifunctional Hydrogel for Sustained Anti-Inflammation and Pain Relief in Lumbar Disc Herniation.

IF 10 2区 医学 Q1 ENGINEERING, BIOMEDICAL Advanced Healthcare Materials Pub Date : 2024-07-09 DOI:10.1002/adhm.202401227
Wenhao Deng, Jianpeng Chen, Xinli Wang, Qianliang Wang, Lei Zhao, Yuzheng Zhu, Jun Yan, Yiran Zheng
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Abstract

Pain caused by lumbar disc herniation (LDH) severely compromises patients' quality of life. The combination of steroid and local anesthetics is routinely employed in clinics to alleviate LDH-induced pain. However, the approach only mediates transient efficacy and requires repeated and invasive lumbar epidural injections. Here a paravertebrally-injected multifunctional hydrogel that can efficiently co-load and controlled release glucocorticoid betamethasone and anesthetics ropivacaine for sustained anti-inflammation, reactive oxygen species (ROS)-removal and pain relief in LDH is presented. Betamethasone is conjugated to hyaluronic acid (HA) via ROS-responsive crosslinker to form amphiphilic polymer that self-assemble into particles with ropivacaine loaded into the core. Solution of drug-loaded particles and thermo-sensitive polymer rapidly forms therapeutic hydrogel in situ upon injection next to the herniated disc, thus avoiding invasive epidural injection. In a rat model of LDH, multifunctional hydrogel maintains the local drug concentration 72 times longer than free drugs and more effectively inhibits the expression of pro-inflammatory cytokines and pain-related molecules including cyclooxygenase-2 (COX-2) and prostaglandin E2 (PGE2). Therapeutic hydrogel suppresses the LDH-induced pain in rats for 12 days while the equivalent dose of free drugs is only effective for 3 days. This platform is also applicable to ameliorate pain caused by other spine-related diseases.

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椎旁注射多功能水凝胶用于腰椎间盘突出症的持续抗炎和止痛。
腰椎间盘突出症(LDH)引起的疼痛严重影响了患者的生活质量。临床上通常采用类固醇和局部麻醉剂相结合的方法来缓解 LDH 引起的疼痛。然而,这种方法只能起到短暂的疗效,而且需要反复进行侵入性腰椎硬膜外注射。本文介绍了一种椎旁注射多功能水凝胶,这种水凝胶能有效地共同负载和控制释放糖皮质激素倍他米松和麻醉剂罗哌卡因,以持续抗炎、清除活性氧(ROS)和缓解 LDH 引起的疼痛。倍他米松通过 ROS 反应性交联剂与透明质酸(HA)共轭,形成两亲性聚合物,这种聚合物可自组装成颗粒,颗粒核心装有罗哌卡因。载药颗粒和热敏聚合物的溶液在注射到椎间盘突出部位后可迅速在原位形成治疗性水凝胶,从而避免了硬膜外注射的侵入性。在大鼠 LDH 模型中,多功能水凝胶保持局部药物浓度的时间是游离药物的 72 倍,并能更有效地抑制促炎细胞因子和疼痛相关分子(包括环氧化酶 2 (COX-2) 和前列腺素 E2 (PGE2))的表达。治疗性水凝胶能在 12 天内抑制 LDH 引起的大鼠疼痛,而同等剂量的游离药物仅能在 3 天内有效。该平台还可用于改善其他脊柱相关疾病引起的疼痛。
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来源期刊
Advanced Healthcare Materials
Advanced Healthcare Materials 工程技术-生物材料
CiteScore
14.40
自引率
3.00%
发文量
600
审稿时长
1.8 months
期刊介绍: Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.
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