Stiff, Multistimuli-Responsive Supramolecular Hydrogels as Unique Molds for 2D/3D Microarchitectures of Live Cells

被引:36
|
作者
Komatsu, Harunobu [1 ]
Tsukiji, Shinya [1 ,2 ]
Ikeda, Masato [1 ]
Hamachi, Itaru [1 ,2 ]
机构
[1] Kyoto Univ, Dept Synthet Chem & Biol Chem, Grad Sch Engn, Kyoto 6158510, Japan
[2] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Chiyoda Ku, Tokyo 1020075, Japan
关键词
cell culture; hydrogels; self-assembly; supramolecular chemistry; zwitterions; PEPTIDE-AMPHIPHILE NANOFIBERS; DELIVERY; DESIGN; DIFFERENTIATION; ENCAPSULATION; FABRICATION; TRANSITION; GELATION;
D O I
10.1002/asia.201100134
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supramolecular hydrogels constructed through molecular self-assembly of small molecules have unique stimuli-responsive properties; however, they are mechanically weak in general, relative to conventional polymer gels. Very recently, we developed a zwitterionic amino acid tethered amphiphilic molecule 1, which gave rise to a remarkably stiff hydrogel comparable with polymer-based agarose gel, retaining reversible thermal-responsive properties. In this study, we describe that rational accumulation of multiple and orthogonal noncovalent interactions in the supramolecular nanofibers of 1 played crucial roles not only in the mechanical reinforcement but also in the multistimuli responsiveness. That is, the zwitterionic amino acid moiety and the C-C double bond unit of the hydrogelator 1 can function as a pH-responsive unit and a light-responsive unit, respectively. We also demonstrated that this stiff and multistimuli-responsive supra-molecular hydrogel 1 is applied as a unique mold for 2D and 3D-patterning of various substances. More significantly, we succeeded in the fabrication of a collagen gel for spatial patterning, culturing, and differentiation of live cells by using hydrogel 1 molds equipped with 2D/3D microspace channels (100-200 mm in diameter).
引用
收藏
页码:2368 / 2375
页数:8
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