Hydrogelation from Self-Assembled and Scaled-Down Chitin Nanofibers by the Modification of Highly Polar Substituents

被引:4
|
作者
Kadokawa, Jun-ichi [1 ]
机构
[1] Kagoshima Univ, Grad Sch Sci & Engn, 1 21 40 Korimoto, Kagoshima 8900065, Japan
关键词
chitin; highly polar substituent; hydrogelation; nanofiber; network structure; physical crosslinking; POLYSACCHARIDE MATERIALS; BIOMEDICAL APPLICATIONS; IONIC LIQUIDS; CHITOSAN; POLY(2-OXAZOLINE)S; PHOSPHORYLASE; DISSOLUTION; FILM; POLYMERIZATION; FABRICATION;
D O I
10.3390/gels9060432
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Chitin nanofibers (ChNFs) with a bundle structure were fabricated via regenerative self-assembly at the nanoscale from a chitin ion gel with an ionic liquid using methanol. Furthermore, the bundles were disentangled by partial deacetylation under alkaline conditions, followed by cationization and electrostatic repulsion in aqueous acetic acid to obtain thinner nanofibers called scaled-down ChNFs. This review presents a method for hydrogelation from self-assembled and scaled-down ChNFs by modifying the highly polar substituents on ChNFs. The modification was carried out by the reaction of amino groups on ChNFs, which were generated by partial deacetylation, with reactive substituent candidates such as poly(2-oxazoline)s with electrophilic living propagating ends and mono- and oligosaccharides with hemiacetallic reducing ends. The substituents contributed to the formation of network structures from ChNFs in highly polar dispersed media, such as water, to produce hydrogels. Moreover, after the modification of the maltooligosaccharide primers on ChNFs, glucan phosphorylase-catalyzed enzymatic polymerization was performed from the primer chain ends to elongate the amylosic graft chains on ChNFs. The amylosic graft chains formed double helices between ChNFs, which acted as physical crosslinking points to construct network structures, giving rise to hydrogels.
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页数:12
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