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Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts
Modifying the surface of the transmucosal area is a key research area because this process positively affects the three functions of implants: attachment to soft tissue, inhibiting bacterial biofilm adhesion, and the preservation of the crestal bone. To exploit the potential of titania nanotube arra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949701/ https://www.ncbi.nlm.nih.gov/pubmed/24623977 http://dx.doi.org/10.2147/IJN.S55514 |
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author | Liu, Xiangning Zhou, Xiaosong Li, Shaobing Lai, Renfa Zhou, Zhiying Zhang, Ye Zhou, Lei |
author_facet | Liu, Xiangning Zhou, Xiaosong Li, Shaobing Lai, Renfa Zhou, Zhiying Zhang, Ye Zhou, Lei |
author_sort | Liu, Xiangning |
collection | PubMed |
description | Modifying the surface of the transmucosal area is a key research area because this process positively affects the three functions of implants: attachment to soft tissue, inhibiting bacterial biofilm adhesion, and the preservation of the crestal bone. To exploit the potential of titania nanotube arrays (TNTs) with or without using bovine serum albumin (BSA) to modify the surface of a dental implant in contact with the transmucosal area, BSA was loaded into TNTs that were fabricated by anodizing Ti sheets; the physical characteristics of these arrays, including their morphology, chemical composition, surface roughness, contact angle, and surface free energy (SFE), were assessed. The effect of Ti surfaces with TNTs or TNTs-BSA on human gingival fibroblasts (HGFs) was determined by analyzing cell morphology, early adhesion, proliferation, type I collagen (COL-1) gene expression, and the extracellular secretion of COL-1. The results indicate that early HGF adhesion and spreading behavior is positively correlated with surface characteristics, including hydrophilicity, SFE, and surface roughness. Additionally, TNT surfaces not only promoted early HGF adhesion, but also promoted COL-1 secretion. BSA-loaded TNT surfaces promoted early HGF adhesion, while suppressing late proliferation and COL-1 secretion. Therefore, TNT-modified smooth surfaces are expected to be applicable for uses involving the transmucosal area. Further study is required to determine whether BSA-loaded TNT surfaces actually affect closed loop formation of connective tissue because BSA coating actions in vivo are very rapid. |
format | Online Article Text |
id | pubmed-3949701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39497012014-03-12 Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts Liu, Xiangning Zhou, Xiaosong Li, Shaobing Lai, Renfa Zhou, Zhiying Zhang, Ye Zhou, Lei Int J Nanomedicine Modifying the surface of the transmucosal area is a key research area because this process positively affects the three functions of implants: attachment to soft tissue, inhibiting bacterial biofilm adhesion, and the preservation of the crestal bone. To exploit the potential of titania nanotube arrays (TNTs) with or without using bovine serum albumin (BSA) to modify the surface of a dental implant in contact with the transmucosal area, BSA was loaded into TNTs that were fabricated by anodizing Ti sheets; the physical characteristics of these arrays, including their morphology, chemical composition, surface roughness, contact angle, and surface free energy (SFE), were assessed. The effect of Ti surfaces with TNTs or TNTs-BSA on human gingival fibroblasts (HGFs) was determined by analyzing cell morphology, early adhesion, proliferation, type I collagen (COL-1) gene expression, and the extracellular secretion of COL-1. The results indicate that early HGF adhesion and spreading behavior is positively correlated with surface characteristics, including hydrophilicity, SFE, and surface roughness. Additionally, TNT surfaces not only promoted early HGF adhesion, but also promoted COL-1 secretion. BSA-loaded TNT surfaces promoted early HGF adhesion, while suppressing late proliferation and COL-1 secretion. Therefore, TNT-modified smooth surfaces are expected to be applicable for uses involving the transmucosal area. Further study is required to determine whether BSA-loaded TNT surfaces actually affect closed loop formation of connective tissue because BSA coating actions in vivo are very rapid. Dove Medical Press 2014-03-06 /pmc/articles/PMC3949701/ /pubmed/24623977 http://dx.doi.org/10.2147/IJN.S55514 Text en © 2014 Liu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Liu, Xiangning Zhou, Xiaosong Li, Shaobing Lai, Renfa Zhou, Zhiying Zhang, Ye Zhou, Lei Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title | Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title_full | Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title_fullStr | Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title_full_unstemmed | Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title_short | Effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
title_sort | effects of titania nanotubes with or without bovine serum albumin loaded on human gingival fibroblasts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949701/ https://www.ncbi.nlm.nih.gov/pubmed/24623977 http://dx.doi.org/10.2147/IJN.S55514 |
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