Hydrophilic-Hydrophobic-Transition-Triggered Thermosensitive Macroscopic Gel Assembly

被引:6
作者
Peng, Yan [1 ]
Wang, Zong-Chun [1 ]
Xu, Xiao-Ding [2 ,3 ]
Song, Jin-Chun [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Pharm, Wuhan 430060, Peoples R China
[2] Wuhan Univ, Key Lab Biomed Polymers, Minist Educ, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
host-guest systems; gels; self-assembly; thermosensitive materials; HOST-GUEST INTERACTIONS; SELF-HEALING MATERIALS; MOLECULAR RECOGNITION; TEMPERATURE; HYDROGELS; POLY(N-ISOPROPYLACRYLAMIDE); POLYMERS; SELECTIVITY; COMPONENTS;
D O I
10.1002/macp.201300445
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two kinds of poly(N-isopropylacrylamide) (PNIPAAm)-based hydrogels containing -cyclodextrin (-CD) (host gel) and benzyl (guest gel) groups, respectively, are designed and prepared. When mixing the host and guest gels together, due to the presence of the host-guest interaction between the -CD and benzyl groups, a combined hydrogel can be formed at a temperature below the lower critical solution temperature (LCST) via macroscopic self-assembly.When heating this self-assembling system to a temperature above the LCST, the aggregation of the hydrophobic PNIPAAm-based chains pull the -CD and benzyl groups to separate them from each other, leading to the disassociation of the combined hydrogel. Because of the transition from hydrophobic aggregated PNIPAAm-based chains to hydrophilic extended ones as the temperature decreases to a value below LCST, the combined hydrogel can re-form via macroscopic self-assembly between the host and guest gels. The concept of hydrophilic-hydrophobic transition-triggered thermosensitive macroscopic self-assembly can be extended to develop many other stimuli-responsive materials.
引用
收藏
页码:2398 / 2404
页数:7
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