羧甲基纤维素
自愈水凝胶
偶氮苯
自愈
琼脂糖
光异构化
环糊精
化学
紫外线
控制释放
高分子化学
材料科学
化学工程
异构化
纳米技术
光化学
有机化学
色谱法
医学
聚合物
催化作用
钠
替代医学
病理
工程类
作者
Yohan Kim,Daham Jeong,Vijay Vilas Shinde,Yiluo Hu,Chulgu Kim,Seunho Jung
标识
DOI:10.1016/j.ijbiomac.2020.07.071
摘要
In this study, multifunctional hydrogels containing host-guest complex formation between azobenzene-grafted carboxymethyl cellulose (CMC-Azo) and β-cyclodextrin (CD) dimers connected by disulfide bonds with agarose for structural support were prepared. The obtained hydrogels exhibited self-healing properties by host-guest complexation as well as gel-sol phase transition in response to ultraviolet (UV) light and reducing agents. Photo-switchable properties of the hydrogels depend on changes in the complex formation of CD-dimers through the trans(450 nm) to cis(365 nm) photo-isomerization of azobenzene. The tensile and strain sweep tests confirmed that the hydrogel's self-healing ability was 79.44% and 81.59%, respectively. In addition, drug release from the hydrogels was controlled to accelerate to 80% in 3 h using UV light or reducing agent. Since the suggested photo-switchable, reduction-responsive, and self-healable hydrogels are non-cytotoxic, they can be potentially applied as biomedical materials in the development of hydrogel-based drug release systems.
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