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非共价相互作用实现自修复水凝胶:罗哌卡因与低分子量凝胶因子脱氧胆酸钠的相互作用,在体内达到稳定持久的局部镇痛效果。

Self-Healing Hydrogel Resulting from the Noncovalent Interaction between Ropivacaine and Low-Molecular-Weight Gelator Sodium Deoxycholate Achieves Stable and Endurable Local Analgesia in Vivo.

机构信息

Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

National Narcotic Laboratory Zhejiang Regional Center, Hangzhou 310000, China.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 4;16(35):45969-45988. doi: 10.1021/acsami.4c07883. Epub 2024 Aug 22.

Abstract

Regional analgesia based on the local anesthetic ropivacaine plays a crucial role in postoperative pain management and recovery; however, the short duration of analgesia limits its clinical potential. Various drug delivery systems such as microparticles and lipid carriers have been used to prolong the analgesic effect, yet most of them are prone to abrupt release from the site of administration or have poor analgesic effects of less than 48 h, which fail to meet the needs of postoperative analgesia. In this study, a low-molecular-weight gelator sodium deoxycholate-based hydrogel loaded with ropivacaine (DC-ROP gel) was designed for long-acting analgesia. The noncovalent interaction between ropivacaine and sodium deoxycholate helps to improve the stability and sustained release performance of the gel. This internal drug-binding hydrogel also avoids experiencing the burst release effect commonly seen in polymer hydrogels previously reported for the slow release of local anesthetics. DC-ROP gel exhibited the dual advantages of self-healing after compression and long-term controlled release. In mice with inflammatory pain, DC-ROP gel achieved peripheral nerve block for more than 1 week after a single injection. Histological and blood biochemical analyses confirmed that the DC-ROP gel did not produce systemic toxicity, and cytotoxicity experiments demonstrated that the DC-ROP gel resulted in low irritation. These results suggest that DC-ROP gel provides a promising strategy for local anesthetics in long-term postoperative pain management, broadening the potential of bile salt-based low-molecular-weight hydrogels for drug delivery.

摘要

基于局部麻醉药罗哌卡因的区域麻醉在术后疼痛管理和康复中起着至关重要的作用;然而,其镇痛作用的持续时间较短限制了其临床应用潜力。各种药物传递系统,如微球和脂质载体,已被用于延长镇痛效果,但它们大多数容易从给药部位突然释放,或者镇痛效果不佳,持续时间不到 48 小时,无法满足术后镇痛的需求。在本研究中,设计了一种基于低分子量凝胶剂脱氧胆酸钠的载罗哌卡因水凝胶(DC-ROP 凝胶)用于长效镇痛。罗哌卡因和脱氧胆酸钠之间的非共价相互作用有助于提高凝胶的稳定性和持续释放性能。这种内部药物结合水凝胶还避免了先前报道的聚合物水凝胶中常见的局部麻醉剂的突释效应,从而实现了缓慢释放。DC-ROP 凝胶具有压缩后自修复和长期控制释放的双重优势。在炎症性疼痛的小鼠中,单次注射后,DC-ROP 凝胶实现了超过 1 周的外周神经阻滞。组织学和血液生化分析证实 DC-ROP 凝胶没有产生全身毒性,细胞毒性实验表明 DC-ROP 凝胶的刺激性较低。这些结果表明,DC-ROP 凝胶为局部麻醉药在长期术后疼痛管理中提供了一种有前途的策略,拓宽了基于胆汁盐的低分子量水凝胶在药物传递中的应用潜力。

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