Photo-induced programmable degradation of carboxymethyl chitosan-based hydrogels

被引:18
|
作者
Wei, Qingcong [1 ]
Bai, Jiahao [1 ]
Wang, Huan [1 ]
Ma, Guanglei [1 ]
Li, Xinjuan [1 ]
Zhang, Weiwei [1 ]
Hu, Zhiguo [1 ]
机构
[1] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Henan Engn Lab Chem Pharmaceut & Biomed Mat, Key Lab Green Chem Media & React,Minist Educ,Sch, Xinxiang 453007, Henan, Peoples R China
关键词
Hydrogel; Carboxymethyl chitosan; Sequential degradation; Photo-responsive; SELF-HEALING HYDROGEL; INJECTABLE HYDROGELS; ANTIBACTERIAL; POLYMER; GEL; REPAIR; WATER;
D O I
10.1016/j.carbpol.2020.117609
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hydrogels are widely used in the biomedical field, due to their high similarity to native extracellular matrix (ECM). Most responsive hydrogels could only passively receive stimuli and independently change their properties. In this study, a photosensitive o-nitrobenzyl (NB) ester linker of polyethylene glycol (PEG) with maleimido (Mal) as terminal groups (PEG-NB-Mal) and a 5-methylfurfuryl (mF) grafted carboxymethyl chitosan (CMCS) derivative (CMCS-mF) were synthesized and used to prepare functional hydrogels via Diels-Alder (DA) reactions. The hydrogel exhibited programmable degradation properties after sequential exposure to UV light and acid treatments. It can maintain high integrity upon the single stimuli, the cascade acid and UV light treatments or the cascade UV light and alkaline treatments. Moreover, the hydrogel exhibited well controlled release profile of rhodamine B (RB). In summary, such CMCS-based hydrogels show great potential in biomedical applications. In addition, the usage of photo-induced cascade reaction in sequential degradation hydrogels can be extended to design other types of programmable smart materials.
引用
收藏
页数:8
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