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RESEARCH ARTICLE
Copyright © 2010 American Scientific Publishers
All rights reserved
Printed in the United States of America
Journal of
Bionanoscience
Vol. 4, 87–91, 2010
An Investigation on the Effect of Morphologies on
Corrosion Behaviour of Nanostructured
Hydroxyapatite-Titania Scaffolds
Simantini Nayak
†
, Kamala Kanta Nanda, Purna C. Rath,
Sarama Bhattacharjee, and Yatendra S. Chaudhary
∗‡
Colloids and Materials Chemistry Department, Institute of Minerals and Materials Technology (CSIR),
Bhubaneswar 751013, India
The viable application of hydroxyapatite (HAp) scaffolds requires to posses the unison of properties:
porosity, bioactivity, mechanical toughness etc. Such properties strongly depend on the geometric
factors such as the size, morphology/microstructure of HAp. We have developed a hydrothermal
based approach to synthesize HAp-titania scaffold with different morphologies ranging from smooth
film to cauliflower to urchin like structures. The structural characterization by XRD reveals the for-
mation of HAp phase. The SEM analysis suggests the formation of HAp nanosheets or their sub-
sequent assembly when reaction carried out under basic conditions without and with the oxidizing
agent H
2
O
2
, respectively. The detailed investigation of corrosion behaviour of all HAp-titania scaffold
samples was undertaken by potentiodynamic technique in Ringer’s simulated body fluid solution at
close to human body temperature i.e., 37
C. The shift in the OCP values of HAp-titania scaffold
samples towards nobler side and the relatively more posivite E
corr
values observed for these sam-
ples than that of bare Ti-foil, suggesting superior corrosion resistance in case of HAp-titania scaffold
samples than that of bare Ti-foil. The detailed results on structural characterization and discussion
on corrosion behaviour of HAp-titania scaffold samples with different morphologies/microstructures
are presented.
Keywords: Hydroxyapatite, Nanostructure, Simulated Body Fluid, Corrosion, Scaffold.
1. INTRODUCTION
The Titanium and its alloys have found extensive appli-
cations as orthopedic implants in human body because
of their higher strength than that of polymeric implants
and high toughness than that of ceramic implants.
1
How-
ever these metallic materials are susceptible to corrosion
by body fluids, which may lead to infection, local pain,
swelling and loosening and consequently the in vivo fail-
ure of implant.
2
The human body shows natural reaction
against prosthetic devices causing the osteolysis and has
the tendency to isolate from the surrounding live tissues.
Moreover, metallic surfaces are not adequately bioactive,
in general, and surface modification is usually required
∗
Author to whom correspondence should be addressed.
†
Present address: Max-Planck-Institut für Eisenforschung, Düsseldorf,
D-40237, Germany.
‡
Present address: Department of Chemistry, University of Oxford, South
Parks Road, OX1 3QR, U.K.
to improve the bioactivity so as to improve osteointegra-
tion with bone tissues. To overcome these problems, Ti
implants are generally coated with bio-active hydroxya-
patite [(Ca
10
(PO
4
6
(OH)
2
] (HAp)—a bio-ceramic which
exhibit physico-chemical resemblance with mineral con-
stituents of human bones and teeth.
3
The coating passi-
vates the body fluid to come in direct contact with metal
and hence minimizes the corrosion of implants. The ability
of such HAp coatings helps to integrate implants to bone
and support new bone generation.
4
Further, some in vitro
studies have revealed that the surface parameters of bio
implant scaffold such as topography may play an impor-
tant role in growth of tissue, retaining their integrity, cell
mobility and control over cellular activity.
5
The physico
chemical and bio-physiological activity of HAp coating
strongly depends upon geometrical factors such as particle
size, dimensional anisotropy, morphology and microstruc-
tures etc. Therefore, apart from the mechanical toughness,
the unison of nanocrystalline nature, porosity and bioac-
tivity, such that it may allow the growth of tissues within
J. Bionanosci. 2010, Vol. 4, No. 1/2 1557-7910/2010/4/087/005 doi:10.1166/jbns.2010.1038 87