Department of Chemistry, Tsinghua University, Beijing, 100084, PR China.
Biomacromolecules. 2011 Aug 8;12(8):2894-901. doi: 10.1021/bm200423f. Epub 2011 Jun 30.
An inexpensive, facile, and environmentally benign method has been developed for the preparation of multiresponsive, dynamic, and self-healing chitosan-based hydrogels. A dibenzaldehyde-terminated telechelic poly(ethylene glycol) (PEG) was synthesized and was allowed to form Schiff base linkages between the aldehyde groups and the amino groups in chitosan. Upon mixing the telechelic PEG with chitosan at 20 °C, hydrogels with solid content of 4-8% by mass were generated rapidly in <60 s. Because of the dynamic equilibrium between the Schiff base linkage and the aldehyde and amine reactants, the hydrogels were found to be self-healable and sensitive to many biochemical-stimuli, such as pH, amino acids, and vitamin B6 derivatives. In addition, chitosan could be digested by enzymes such as papain, leading to the decomposition of the hydrogels. Encapsulation and controlled release of small molecules such as rhodamine B and proteins such as lysozyme have been successfully carried out, demonstrating the potential biomedical applications of these chitosan-based dynamic hydrogels.
一种廉价、简便且环境友好的方法被开发出来,用于制备具有多响应性、动态性和自修复功能的壳聚糖基水凝胶。一种二苯甲醛封端的遥爪聚乙二醇(PEG)被合成,并允许醛基和壳聚糖中的氨基之间形成席夫碱键。遥爪 PEG 在 20°C 与壳聚糖混合时,在<60s 内迅速生成质量分数为 4-8%的水凝胶。由于希夫碱键和醛基以及胺反应物之间的动态平衡,水凝胶具有自修复能力,并且对许多生化刺激物(如 pH 值、氨基酸和维生素 B6 衍生物)敏感。此外,壳聚糖可以被木瓜蛋白酶等酶消化,导致水凝胶的分解。成功地进行了小分子如罗丹明 B 和蛋白质如溶菌酶的包封和控制释放,证明了这些基于壳聚糖的动态水凝胶在生物医学中的潜在应用。