Biomimetic synthesis of hydroxyapatite/bacterial cellulose nanocomposites for biomedical applications

被引:276
|
作者
Wan, Y. Z. [1 ]
Huang, Y.
Yuan, C. D.
Raman, S.
Zhu, Y.
Jiang, H. J.
He, F.
Gao, C.
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Chem Engn, Tianjin 300072, Peoples R China
[3] Queens Univ, Dept Epidemiol & Community Hlth, Kingston, ON K7L 3N6, Canada
[4] Wendeng Hosp Orthopaed, Shandong 264400, Peoples R China
关键词
bacterial cellulose; hydroxyapatite; nanocomposite; surface treatment; biomineralization;
D O I
10.1016/j.msec.2006.10.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Hydroxyapatite (HAp) and bacterial cellulose (BC) are both excellent materials for use in biomaterial areas. The former has outstanding osteoconductivity and bioactivity and the latter is a high-strength nano-fibrous and extensively used biomaterial. In this work, the HAp/BC nanocomposites with a 3-dimensional (3-D) network were synthesized via a biological route by soaking both phosphorylated and unphosphorylated BCs in 1.5 simulated body fluid (SBF). Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) were employed to characterize the HAp/BC nanocomposites. SEM observations demonstrated that HAp crystals were uniformly formed on the phosphorylated BC fibers after soaking in 1.5 SBF whereas little HAp was observed on individual unphosphorylated BC fibers. Our experimental results suggested that the unphosphorylated BC did not induce HAp growth and that phosphorylation effectively triggered HAp formation on BC. Mechanisms were proposed for the explanation of the experimental observations. XRD and FTIR results revealed that the HAp crystals formed on the phosphorylated BC fibers were carbonate-containing with nano-sized crystallites and crystallinities less than 1%. These structural features were close to those of biological apatites. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:855 / 864
页数:10
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