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Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility

The lifetime of orthopaedic implants can be extended by coating the softer Ti(6)Al(4)V alloy with harder biocompatible thin films. In this work, thin films of Ti((1-x))Au((x)) are grown on Ti(6)Al(4)V and glass substrates by magnetron sputtering in the entire x = 0–1 range, before their key biomecha...

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Autores principales: Lukose, Cecil Cherian, Anestopoulos, Ioannis, Mantso, Theodora, Bowen, Leon, Panayiotidis, Mihalis I., Birkett, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958427/
https://www.ncbi.nlm.nih.gov/pubmed/35386358
http://dx.doi.org/10.1016/j.bioactmat.2022.02.027
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author Lukose, Cecil Cherian
Anestopoulos, Ioannis
Mantso, Theodora
Bowen, Leon
Panayiotidis, Mihalis I.
Birkett, Martin
author_facet Lukose, Cecil Cherian
Anestopoulos, Ioannis
Mantso, Theodora
Bowen, Leon
Panayiotidis, Mihalis I.
Birkett, Martin
author_sort Lukose, Cecil Cherian
collection PubMed
description The lifetime of orthopaedic implants can be extended by coating the softer Ti(6)Al(4)V alloy with harder biocompatible thin films. In this work, thin films of Ti((1-x))Au((x)) are grown on Ti(6)Al(4)V and glass substrates by magnetron sputtering in the entire x = 0–1 range, before their key biomechanical properties are performance tuned by thermal activation. For the first time, we explore the effect of in-situ substrate heating versus ex-situ post-deposition heat-treatment, on development of mechanical and biocompatibility performance in Ti–Au films. A ∼250% increase in hardness is achieved for Ti–Au films compared to bulk Ti(6)Al(4)V and a ∼40% improvement from 8.8 GPa as-grown to 11.9 and 12.3 GPa with in-situ and ex-situ heat-treatment respectively, is corelated to changes in structural, morphological and chemical properties, providing insights into the origins of super-hardness in the Ti rich regions of these materials. X-ray diffraction reveals that as-grown films are in nanocrystalline states of Ti–Au intermetallic phases and thermal activation leads to emergence of mechanically hard Ti–Au intermetallics, with films prepared by in-situ substrate heating having enhanced crystalline quality. Surface morphology images show clear changes in grain size, shape and surface roughness following thermal activation, while elemental analysis reveals that in-situ substrate heating is better for development of oxide free Ti(3)Au β-phases. All tested Ti–Au films are non-cytotoxic against L929 mouse fibroblast cells, while extremely low leached ion concentrations confirm their biocompatibility. With peak hardness performance tuned to >12 GPa and excellent biocompatibility, Ti–Au films have potential as a future coating technology for load bearing medical implants.
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spelling pubmed-89584272022-04-05 Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility Lukose, Cecil Cherian Anestopoulos, Ioannis Mantso, Theodora Bowen, Leon Panayiotidis, Mihalis I. Birkett, Martin Bioact Mater Article The lifetime of orthopaedic implants can be extended by coating the softer Ti(6)Al(4)V alloy with harder biocompatible thin films. In this work, thin films of Ti((1-x))Au((x)) are grown on Ti(6)Al(4)V and glass substrates by magnetron sputtering in the entire x = 0–1 range, before their key biomechanical properties are performance tuned by thermal activation. For the first time, we explore the effect of in-situ substrate heating versus ex-situ post-deposition heat-treatment, on development of mechanical and biocompatibility performance in Ti–Au films. A ∼250% increase in hardness is achieved for Ti–Au films compared to bulk Ti(6)Al(4)V and a ∼40% improvement from 8.8 GPa as-grown to 11.9 and 12.3 GPa with in-situ and ex-situ heat-treatment respectively, is corelated to changes in structural, morphological and chemical properties, providing insights into the origins of super-hardness in the Ti rich regions of these materials. X-ray diffraction reveals that as-grown films are in nanocrystalline states of Ti–Au intermetallic phases and thermal activation leads to emergence of mechanically hard Ti–Au intermetallics, with films prepared by in-situ substrate heating having enhanced crystalline quality. Surface morphology images show clear changes in grain size, shape and surface roughness following thermal activation, while elemental analysis reveals that in-situ substrate heating is better for development of oxide free Ti(3)Au β-phases. All tested Ti–Au films are non-cytotoxic against L929 mouse fibroblast cells, while extremely low leached ion concentrations confirm their biocompatibility. With peak hardness performance tuned to >12 GPa and excellent biocompatibility, Ti–Au films have potential as a future coating technology for load bearing medical implants. KeAi Publishing 2022-03-03 /pmc/articles/PMC8958427/ /pubmed/35386358 http://dx.doi.org/10.1016/j.bioactmat.2022.02.027 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lukose, Cecil Cherian
Anestopoulos, Ioannis
Mantso, Theodora
Bowen, Leon
Panayiotidis, Mihalis I.
Birkett, Martin
Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title_full Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title_fullStr Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title_full_unstemmed Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title_short Thermal activation of Ti(1-x)Au(x) thin films with enhanced hardness and biocompatibility
title_sort thermal activation of ti(1-x)au(x) thin films with enhanced hardness and biocompatibility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958427/
https://www.ncbi.nlm.nih.gov/pubmed/35386358
http://dx.doi.org/10.1016/j.bioactmat.2022.02.027
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