自愈水凝胶
壳聚糖
甲基丙烯酸酯
乙二醇
吸水率
高分子化学
材料科学
化学工程
化学
复合材料
聚合物
有机化学
共聚物
工程类
作者
Pan Wu,Yaru Fang,Kezhou Chen,Mi Wu,Wenchang Zhang,Shiyu Wang,Dongwen Liu,Junqing Gao,Huaiguo Li,Jianhua Lv,Yan Zhao
标识
DOI:10.1016/j.eurpolymj.2023.112137
摘要
Based on sodium methacrylate alginate (MASA) and carboxymethyl chitosan (CMCS), double network (DN) hydrogels were formed by covalent crosslinking and physical crosslinking in succession. Covalent crosslinking was achieved by using poly(ethylene glycol) diacrylate (PEGDA) as the crosslinker and initiated by ammonium persulfates, while physical crosslinking was realized by the electrostatic interactions between the carboxyl group of MASA and the amino group of CMCS induced by acetic acid atmosphere. With the addition of PEGDA (1.25 wt% of mixture solution), the compressive strength of hydrogel was increased from 9.0 kPa to 73.3 kPa. Compared with the physically cross-linked hydrogels, the light transmittance of the DN hydrogels at 600 nm was significantly increased from 23.7% to 93.8%. The drug release studied by taking berberine hydrochloride hydrate (Ber) as the model drug showed that drug release behaviors of the DN hydrogels were pH sensitive and notably correlated with the content of PEGDA. In addition, DN hydrogels existed excellent water absorption rate (38.3-fold). Therefore, the enhanced mechanical properties, high transparency, excellent water absorption rate, and pH sensitivity of the DN hydrogel suggested the promising applications of the hydrogels as visual transdermal drug delivery systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI