Four distinct network patterns of supramolecular/polymer composite hydrogels controlled by formation kinetics and interfiber interactions

被引:22
|
作者
Nakamura, Keisuke [1 ]
Kubota, Ryou [1 ]
Aoyama, Takuma [2 ,3 ]
Urayama, Kenji [3 ]
Hamachi, Itaru [1 ,4 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Synthet Chem & Biol Chem, Kyoto, Japan
[2] Kyoto Inst Technol, Dept Macromol Sci & Engn, Kyoto, Japan
[3] Kyoto Univ, Grad Sch Engn, Dept Chem Mat, Kyoto, Japan
[4] JST ERATO, Hamachi Innovat Mol Technol Neurosci, Kyoto, Japan
基金
日本科学技术振兴机构;
关键词
MOLECULAR-WEIGHT GELS; EXTRACELLULAR-MATRIX; FATIGUE RESISTANCE; SWELLING PRESSURE; HYBRID HYDROGELS; SOFT MATERIALS; POLYMER; DESIGN;
D O I
10.1038/s41467-023-37412-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synthetic composite hydrogels comprising supramolecular fibers and covalent polymers have attracted considerable attention because their properties are similar to biological connective tissues. However, an in-depth analysis of the network structures has not been performed. In this study, we discovered the composite network can be categorized into four distinct patterns regarding morphology and colocalization of the components using in situ, real-time confocal imaging. Time-lapse imaging of the network formation process reveals that the patterns are governed by two factors, the order of the network formation and the interactions between the two different fibers. Additionally, the imaging studies revealed a unique composite hydrogel undergoing dynamic network remodeling on the scale of a hundred micrometers to more than one millimeter. Such dynamic properties allow for fracture-induced artificial patterning of a network three dimensionally. This study introduces a valuable guideline to the design of hierarchical composite soft materials.
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页数:12
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