Decoupled Thermo- and pH-Responsive Hydrogel Microspheres Cross-Linked by Rotaxane Networks

被引:64
|
作者
Kureha, Takuma [1 ]
Aoki, Daichi [1 ]
Hiroshige, Seina [1 ]
Iijima, Keisuke [4 ,5 ]
Aoki, Daisuke [4 ,5 ]
Takata, Toshikazu [4 ,5 ]
Suzuki, Daisuke [1 ,2 ,3 ]
机构
[1] Shinshu Univ, Grad Sch Text Sci & Technol, 3-15-1 Tokida Ueda, Nagano 3868567, Japan
[2] Shinshu Univ, Inst Fiber Engn Interdisciplinary Cluster Cutting, Div Smart Text, 3-15-1 Tokida Ueda, Nagano 3868567, Japan
[3] JST CREST, 3-15-1 Tokida Ueda, Nagano 3868567, Japan
[4] Tokyo Inst Technol, Dept Chem Sci & Engn, Meguro Ku, 2-12-1 Ookayama, Tokyo 1528552, Japan
[5] JST CREST, Meguro Ku, 2-12-1 Ookayama, Tokyo 1528552, Japan
基金
日本学术振兴会;
关键词
hydrogel microspheres; multi-responsiveness; precipitation polymerization; rotaxane cross-linkers; supramolecular chemistry; CORE-SHELL MICROGELS; N-ISOPROPYLACRYLAMIDE; PARTICLES; COMPLEXES; POLYMERS; BEHAVIOR; DESIGN; CHARGE;
D O I
10.1002/anie.201709633
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rotaxane cross-linked (RC) microgels that exhibit a decoupled thermo- and pH-responsive volume transition were developed. The pH-induced changes of the aggregation/disaggregation states of cyclodextrin in the RC networks were used to control the swelling capacity of the entire microgels. Different from conventional thermo- and pH-responsive microgels, which are usually obtained from copolymerizations involving charged monomers, the RC microgels respond to temperature as intended, even in the presence of charged functional molecules such as dyes in the microgel dispersion. The results of this study should lead to new applications, including drug delivery systems that require a retention of their smart functions even in environments that may contain foreign ions, for example, in invivo experiments.
引用
收藏
页码:15393 / 15396
页数:4
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