Preparation of poly(3-hydroxybutyrate-co-4-hydroxybutyrate)-based composites releasing soluble silica for bone regeneration

被引:5
|
作者
Obata, Akiko [1 ]
Iwata, Takuma [1 ]
Maeda, Hirotaka [2 ]
Hirata, Hitoshi [3 ]
Kasuga, Toshihiro [1 ]
机构
[1] Nagoya Inst Technol, Grad Sch Engn, Showa Ku, Nagoya, Aichi 4668555, Japan
[2] Nagoya Inst Technol, Ctr Fostering Young & Innovat Researchers, Showa Ku, Nagoya, Aichi 4668555, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Hand Surg, Showa Ku, Nagoya, Aichi 4668550, Japan
基金
日本科学技术振兴机构;
关键词
Silica; Poly(3-hydroxybutyrate-co-4-hydroxybutyrate); Composite; TEOS; Elongation; SBF; BIOACTIVE GLASS DISSOLUTION; IN-VITRO; IONIC PRODUCTS; HUMAN OSTEOBLASTS; TISSUE-RESPONSE; PROLIFERATION; POLY(3-HYDROXYBUTYRATE-CO-3-HYDROXYHEXANOATE); POLYHYDROXYALKANOATES; DIFFERENTIATION; DEGRADATION;
D O I
10.2109/jcersj2.121.753
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Silica/poly(3-hydroxybutyrate-co-4-hydroxybutyrate) composites were prepared for achievement of new medical devices having bioactivity, biodegaradability and excellent mechanical-elongation property for the use in bone regeneration. The composites were prepared using three different types of silicon alcoxides, Tetraethylorthosilicate (TEOS), Diethoxydimethylsilane (DEODMS) and 3-aminopropyltriethoxysilane (APTES), as a silica source. The composites prepared with TEOS possessed both abilities of soluble silica releasing and hydroxyapatite forming in simulated body fluid, while the composites prepared with the other sources didn't show them. The chemical structure and tensile properties of the composites prepared with TEOS were evaluated. Fourier transform infrared reflection and 13C cross polarization magic angle spinning nuclear magnetic resonance spectroscopic analyses demonstrated that the crystallinity of polymer phase in the composites was reduced by adding the silica. The composites containing < 25 wt% of silica exhibited a large failure strain (3 700%). (C)2013 The Ceramic Society of Japan. All rights reserved.
引用
收藏
页码:753 / 758
页数:6
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