Title of article :
Biomimetic synthesis of hydroxyapatite/bacterial cellulose nanocomposites for biomedical applications
Author/Authors :
Wan ، نويسنده , , Y.Z. and Huang، نويسنده , , Y. and Yuan، نويسنده , , C.D. and Raman، نويسنده , , S. and Zhu، نويسنده , , Y. and Jiang، نويسنده , , H.J. and He، نويسنده , , F. and Gao، نويسنده , , C.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
10
From page :
855
To page :
864
Abstract :
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.
Keywords :
Bacterial cellulose , Hydroxyapatite , Nanocomposite , Surface treatment , biomineralization
Journal title :
Materials Science and Engineering C
Serial Year :
2007
Journal title :
Materials Science and Engineering C
Record number :
2096634
Link To Document :
بازگشت