4.7 Article

Spectroscopic investigation on formation and growth of mineralized nanohydroxyapatite for bone tissue engineering applications

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2012.02.069

关键词

Substituted hydroxyapatite; Bioceramics; Nanomaterial; Bio-mineralization; Biomedical applications; Tissue engineering applications

资金

  1. Indian Council of Medical Research (ICMR, IRIS) [2010-08660, 5/20/11(Bio)/10-NCD-1]
  2. Department of Science and Technology, New Delhi, India (DST-SERC) [SR/FTP/ETA-04/2009]
  3. DST-TSD [DST/TSG/NTS/2011/73]
  4. CSIR [01(2547)/11/EMR-11]
  5. ICTP, Italy
  6. Periyar University

向作者/读者索取更多资源

Synthetic calcium hydroxyapatite (HAP,Ca-10(PO4)(6)(OH)(2)) is a well-known bioceramic material used in orthopaedic and dental applications because of its excellent biocompatibility and bone-bonding ability. Substitution of trace elements, such as Sr, Mg and Zn ions into the structure of calcium phosphates is the subject of widespread investigation. In this paper, we have reported the synthesis of Sr, Mg and Zn co-substituted nanohydroxyapatite by soft solution freezing method. The effect of pH on the morphology of bioceramic nanomaterial was also discussed. The in vitro bioactivity of the as-synthesized bioceramic nanomaterial was determined by soaking it in SBF for various days. The as-synthesized bioceramic nanomaterial was characterized by Fourier transform infrared spectroscopy, X-ray diffraction analysis, Scanning electron microscopy and Energy dispersive X-ray analysis and Transmission electron microscopic techniques respectively. The results obtained in our study have revealed that pH 10 was identified to induce the formation of mineralized nanohydroxyapatite. It is observed that the synthesis of bioceramic nanomaterial not only support the growth of apatite layer on its surface but also accelerate the growth which is evident from the in vitro studies. Therefore, mineralized nanohydroxyapatite is a potential candidate in bone tissue engineering. (C) 2012 Elsevier B.V. All rights reserved.

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