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MWCNTs as reinforcing agent to the Hap-Gel nanocomposite for artificial bone grafting
The essence of this investigation is to explore MWCNTs as reinforcing agents to strengthen Hap–Gel nanocomposites for artificial bone grafting applications without significantly compromising their biocompatibility. Hap–Gelatin composites, reinforced with various proportions of MWCNTs, were synthesiz...
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Published in: | Journal of biomedical materials research. Part A 2010-06, Vol.93A (3), p.886-896 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The essence of this investigation is to explore MWCNTs as reinforcing agents to strengthen Hap–Gel nanocomposites for artificial bone grafting applications without significantly compromising their biocompatibility. Hap–Gelatin composites, reinforced with various proportions of MWCNTs, were synthesized to optimize the MWCNT content in the composites which yield commendable improvement in the strength. The morphological studies reveal that the MWCNTs act as templates for nucleation of Hap crystals. The biocompatibility of MWCNT reinforced Hap–Gelatin composites were evaluated in animal model through the histopathological investigation of tissues from skin, kidney, and liver. On histopathological examination, no noticeable alteration due to toxicity was found for lower concentration of MWCNTs. Mild reversible changes in the liver and tubular damage in kidney have been observed for higher concentration (4 wt % of MWCNTs). It can be inferred from the findings that MWCNTs, in proportions less than 4%, can successfully be used to reinforce the Hap–Gel nanocomposite to improve its mechanical properties. However, how safe would these CNT reinforced bone implants would be when used for prolonged period in actual physiological conditions needs to be investigated further. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010 |
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ISSN: | 1549-3296 1552-4965 1552-4965 |
DOI: | 10.1002/jbm.a.32581 |