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Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions

Current titanium-based implants are often anodized in sulfuric acid (H(2)SO(4)) for color coding purposes. However, a crucial parameter in selecting the material for an orthopedic implant is the degree to which it will integrate into the surrounding bone. Loosening at the bone–implant interface can...

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Autores principales: Ross, Alexandra P, Webster, Thomas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540959/
https://www.ncbi.nlm.nih.gov/pubmed/23319862
http://dx.doi.org/10.2147/IJN.S36203
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author Ross, Alexandra P
Webster, Thomas J
author_facet Ross, Alexandra P
Webster, Thomas J
author_sort Ross, Alexandra P
collection PubMed
description Current titanium-based implants are often anodized in sulfuric acid (H(2)SO(4)) for color coding purposes. However, a crucial parameter in selecting the material for an orthopedic implant is the degree to which it will integrate into the surrounding bone. Loosening at the bone–implant interface can cause catastrophic failure when motion occurs between the implant and the surrounding bone. Recently, a different anodization process using hydrofluoric acid has been shown to increase bone growth on commercially pure titanium and titanium alloys through the creation of nanotubes. The objective of this study was to compare, for the first time, the influence of anodizing a titanium alloy medical device in sulfuric acid for color coding purposes, as is done in the orthopedic implant industry, followed by anodizing the device in hydrofluoric acid to implement nanotubes. Specifically, Ti6Al4V model implant samples were anodized first with sulfuric acid to create color-coding features, and then with hydrofluoric acid to implement surface features to enhance osteoblast functions. The material surfaces were characterized by visual inspection, scanning electron microscopy, contact angle measurements, and energy dispersive spectroscopy. Human osteoblasts were seeded onto the samples for a series of time points and were measured for adhesion and proliferation. After 1 and 2 weeks, the levels of alkaline phosphatase activity and calcium deposition were measured to assess the long-term differentiation of osteoblasts into the calcium depositing cells. The results showed that anodizing in hydrofluoric acid after anodizing in sulfuric acid partially retains color coding and creates unique surface features to increase osteoblast adhesion, proliferation, alkaline phosphatase activity, and calcium deposition. In this manner, this study provides a viable method to anodize an already color coded, anodized titanium alloy to potentially increase bone growth for numerous implant applications.
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spelling pubmed-35409592013-01-14 Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions Ross, Alexandra P Webster, Thomas J Int J Nanomedicine Original Research Current titanium-based implants are often anodized in sulfuric acid (H(2)SO(4)) for color coding purposes. However, a crucial parameter in selecting the material for an orthopedic implant is the degree to which it will integrate into the surrounding bone. Loosening at the bone–implant interface can cause catastrophic failure when motion occurs between the implant and the surrounding bone. Recently, a different anodization process using hydrofluoric acid has been shown to increase bone growth on commercially pure titanium and titanium alloys through the creation of nanotubes. The objective of this study was to compare, for the first time, the influence of anodizing a titanium alloy medical device in sulfuric acid for color coding purposes, as is done in the orthopedic implant industry, followed by anodizing the device in hydrofluoric acid to implement nanotubes. Specifically, Ti6Al4V model implant samples were anodized first with sulfuric acid to create color-coding features, and then with hydrofluoric acid to implement surface features to enhance osteoblast functions. The material surfaces were characterized by visual inspection, scanning electron microscopy, contact angle measurements, and energy dispersive spectroscopy. Human osteoblasts were seeded onto the samples for a series of time points and were measured for adhesion and proliferation. After 1 and 2 weeks, the levels of alkaline phosphatase activity and calcium deposition were measured to assess the long-term differentiation of osteoblasts into the calcium depositing cells. The results showed that anodizing in hydrofluoric acid after anodizing in sulfuric acid partially retains color coding and creates unique surface features to increase osteoblast adhesion, proliferation, alkaline phosphatase activity, and calcium deposition. In this manner, this study provides a viable method to anodize an already color coded, anodized titanium alloy to potentially increase bone growth for numerous implant applications. Dove Medical Press 2013 2013-01-04 /pmc/articles/PMC3540959/ /pubmed/23319862 http://dx.doi.org/10.2147/IJN.S36203 Text en © 2013 Ross and Webster, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Ross, Alexandra P
Webster, Thomas J
Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title_full Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title_fullStr Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title_full_unstemmed Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title_short Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions
title_sort anodizing color coded anodized ti6al4v medical devices for increasing bone cell functions
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540959/
https://www.ncbi.nlm.nih.gov/pubmed/23319862
http://dx.doi.org/10.2147/IJN.S36203
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