Li Lin, Wang Ya
Guangdong Provincial/Zhuhai Key Laboratory of IRADS, and Department of Life Sciences, BNU-HKBU United International College, Zhuhai 519087, China.
Polymers (Basel). 2025 Mar 14;17(6):780. doi: 10.3390/polym17060780.
Glycemic management in diabetes patients remains heavily reliant on multiple daily insulin injections, which often leads to poor patient compliance and an elevated risk of hypoglycemia. To overcome these limitations, injectable hydrogels capable of encapsulating insulin within polymeric networks have emerged as a promising alternative. Ideally, a single injection can form an in situ depot that allows prolonged glycemic control and lower injection frequency. This review summarizes recent advances in injectable hydrogels for controlled insulin delivery, focusing on the polymer sources, crosslinking strategies, and stimuli-responsive release mechanisms. Synthetic polymers such as PEG, PNIPAM, and Pluronics dominate the current research due to their highly tunable properties, whereas naturally derived polysaccharides and proteins generally require further modifications for enhanced functionality. The crosslinking types, ranging from relatively weak physical interactions (hydrogen bonds, hydrophobic interactions, etc.) to dynamic covalent bonds with higher binding strength (e.g., Schiff base, phenylboronate ester), significantly influence the shear-thinning behavior and stimuli-responsiveness of hydrogel systems. Hydrogels' responsiveness to temperature, glucose, pH, and reactive oxygen species has enabled more precise insulin release, offering new options for improved diabetic management. Beyond glycemic regulation, this review also explores insulin-loaded hydrogels for treating complications. Despite the progress, challenges such as burst release, long-term biocompatibility, and scalability remain. Future research should focus on optimizing hydrogel design, supported by robust and comprehensive data.
糖尿病患者的血糖管理仍然严重依赖于每日多次胰岛素注射,这往往导致患者依从性差以及低血糖风险升高。为了克服这些局限性,能够将胰岛素包裹在聚合物网络中的可注射水凝胶已成为一种有前景的替代方案。理想情况下,单次注射即可形成原位 depot,实现长期血糖控制并降低注射频率。本综述总结了用于可控胰岛素递送的可注射水凝胶的最新进展,重点关注聚合物来源、交联策略和刺激响应释放机制。诸如聚乙二醇(PEG)、聚N-异丙基丙烯酰胺(PNIPAM)和普朗尼克(Pluronics)等合成聚合物因其高度可调节的性质主导了当前的研究,而天然衍生的多糖和蛋白质通常需要进一步修饰以增强功能。交联类型从相对较弱的物理相互作用(氢键、疏水相互作用等)到具有更高结合强度的动态共价键(例如席夫碱、苯基硼酸酯),显著影响水凝胶系统的剪切变稀行为和刺激响应性。水凝胶对温度、葡萄糖、pH值和活性氧的响应能够实现更精确的胰岛素释放,为改善糖尿病管理提供了新的选择。除了血糖调节,本综述还探讨了用于治疗并发症的载胰岛素水凝胶。尽管取得了进展,但诸如突释、长期生物相容性和可扩展性等挑战仍然存在。未来的研究应侧重于在强大而全面的数据支持下优化水凝胶设计。