Do 'passive' medical titanium surfaces deteriorate in service in the absence of wear?

Addison, O. and Davenport, A.J. and Newport, Robert J. and Kalra, S. and Monir, M. and Mosselmans, J.F.W. and Proops, D. and Martin, R.A. (2012) Do 'passive' medical titanium surfaces deteriorate in service in the absence of wear? Journal of the Royal Society Interface, 9 (76). pp. 3161-3164. ISSN 17425689 (ISSN). (doi:https://doi.org/10.1098/rsif.2012.0438) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided)

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Abstract

Globally, more than 1000 tonnes of titanium (Ti) is implanted into patients in the form of biomedical devices on an annual basis. Ti is perceived to be 'biocompatible' owing to the presence of a robust passive oxide film (approx. 4 nm thick) at the metal surface. However, surface deterioration can lead to the release of Ti ions, and particles can arise as the result of wear and/or corrosion processes. This surface deterioration can result in peri-implant inflammation, leading to the premature loss of the implanted device or the requirement for surgical revision. Soft tissues surrounding commercially pure cranial anchorage devices (bone-anchored hearing aid) were investigated using synchrotron X-ray micro-fluorescence spectroscopy and X-ray absorption near edge structure. Here, we present the first experimental evidence that minimal load-bearing Ti implants, which are not subjected to macroscopic wear processes, can release Ti debris into the surrounding soft tissue. As such debris has been shown to be pro-inflammatory, we propose that such distributions of Ti are likely to effect to the service life of the device. © 2012 The Royal Society.

Item Type: Article
Additional information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - J. R. Soc. Interface [Field not mapped to EPrints] C2 - 22832360 [Field not mapped to EPrints] AD - Biomaterials Unit, School of Dentistry, University of Birmingham, Birmingham, United Kingdom [Field not mapped to EPrints] AD - School of Metallurgy and Materials, University of Birmingham, Birmingham, United Kingdom [Field not mapped to EPrints] AD - School of Physical Sciences, University of Kent, Canterbury, United Kingdom [Field not mapped to EPrints] AD - Science Division, Diamond Light Source, Harwell Science and Innovation Campus, Didcot, United Kingdom [Field not mapped to EPrints] AD - University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom [Field not mapped to EPrints] AD - School of Engineering and Applied Sciences, Aston Research Centre for Healthy Ageing, University of Aston, Birmingham, United Kingdom [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints]
Uncontrolled keywords: Crevice corrosion, Microfocus spectroscopy, Titanium, Biomedical devices, Bone-anchored hearing aids, Corrosion process, Crevice corrosion, Experimental evidence, Implanted device, Load-bearing, Metal surfaces, Passive oxide films, Soft tissue, Surface deterioration, Synchrotron x rays, Titanium surfaces, TO effect, Wear process, X-ray absorption near-edge structure, Debris, Deterioration, Fluorescence spectroscopy, Hearing aids, Implants (surgical), Oxide films, Tissue, X ray absorption near edge structure spectroscopy, Titanium, oxide, titanium, article, biocompatibility, bone anchored hearing aid, corrosion, human, human tissue, implant, implantation, inflammation, medical device, soft tissue, spectroscopy, synchrotron, X ray absorption spectroscopy, X ray micro fluorescence spectroscopy, Biocompatible Materials, Corrosion, Humans, Peri-Implantitis, Prostheses and Implants, Spectrometry, X-Ray Emission, Synchrotrons, Titanium, X-Ray Absorption Spectroscopy
Subjects: Q Science > QC Physics > QC173.45 Condensed Matter
Q Science > QD Chemistry > QD478 Solid State Chemistry
Divisions: Faculties > Sciences > School of Physical Sciences > Functional Materials Group
Depositing User: Giles Tarver
Date Deposited: 12 Feb 2015 11:36 UTC
Last Modified: 19 Feb 2015 15:51 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/46955 (The current URI for this page, for reference purposes)
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