Structural and mechanical characterization of bacterial cellulose-polyethylene glycol diacrylate composite gels

被引:27
作者
Numata, Yukari [1 ]
Kono, Hiroyuki [2 ]
Tsuji, Minato [3 ]
Tajima, Kenji [4 ]
机构
[1] Otaru Univ, Fac Commerce, Gen Educ, 3-5-21 Midori, Otaru, Hokkaido 0478501, Japan
[2] Natl Inst Technol, Div Appl Chem & Biochem, Tomakomai 0591275, Japan
[3] Otaru Univ, Fac Commerce, Dept Commerce, Otaru, Hokkaido 0478501, Japan
[4] Hokkaido Univ, Fac Engn, Div Appl Chem, Sapporo, Hokkaido 0608628, Japan
基金
日本科学技术振兴机构;
关键词
Bacterial cellulose; Polyethylene glycol diacrylate; Soft-material sheet; Biocompatibility; Tactile sensation; MOLECULAR-DYNAMICS; HYDROGELS; BIOSYNTHESIS; WATER;
D O I
10.1016/j.carbpol.2017.05.077
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study explores the structural and mechanical properties of bacterial cellulose-polyethylene glycol diacrylate (BC-PEGDA) composite gels. The molecular dynamics results obtained by solid-state (13) C nuclear magnetic resonance analyses suggested that BC and PEGDA molecules were incompatible as composite gels, though BC fibers and PEGDA interact with each other. The mechanical strength of the gels depended on the amount of PEGDA, becoming softer and more stretchable when a tensile force was applied, but for a large amount of PEGDA, they became brittle. The BC-3% and 5% PEGDA gels had similar viscoelastic behaviors as a BC gel, and these composite gels could stick to human skin. Since BC-PEGDA composite gels are composed of BC and PEGDA-both of which are biocompatible, it is thought that these composite gels also have excellent biocompatibility. Taken together, we concluded that the BC-3% and 5% PEGDA gels have great potential for use in medical and cosmetic fields. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:67 / 76
页数:10
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