Published December 2018 | Version v1
Journal article

Construction novel hydroxyapatite-nitinol nanocomposite for hard tissue applications

  • 1. Department of Material Engineering, Iran University of Science and Technology, Tehran (Iran, Islamic Republic of)
  • 2. National Cell Bank of Iran, Pasteur Institute of Iran, Tehran (Iran, Islamic Republic of)

Description

Highlights: • Improve the mechanical properties of HA is proposed. • Nitinol has been used in HA ceramic to improve its mechanical reliability. • NHA- NiTi nanocomposites were fabricated by powder metallurgy. • The structural stability of HA phase in HA- NiTi samples and mechanical strength of nanocomposites were studied. Natural Hydroxyapatite (HA)- Nitinol (NiTi) nanocomposites with different percentage of NiTi were fabricated by powder metallurgy. The structural stability of HA phase in HA- NiTi samples and mechanical strength of nanocomposites were studied by FTIR, XRD and compression test. In addition, biological behavior of the composites were investigated by in vitro studies. The existence of NiTi metal phase can promote dehydration and decomposition of HA ceramic phase into more stable calcium phosphate phases at high temperatures. According to results that obtained, the nanocomposite sample with 10 wt% NiTi has the maximum compressive strength (67.67 MPa) compare to pure HA ceramic (46 MPa) that manufactured under the same condition. Crack deflection is the chief strength mechanism in the nanocomposites. in vitro studies showed that MG-67 osteoblast cells attached and spread on the surface of the sample. The results revealed that nanocomposite with 10 wt% NiTi has a good mechanical strength and suitable biological behavior that can be used in medical applications.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2018.08.077

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2018.08.077;
PII
S0254058418307429;

Publishing Information

Journal Title
Materials Chemistry and Physics (Print)
Journal Volume
220
Journal Page Range
p. 331-341
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2018 Elsevier B.V. All rights reserved.