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Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces
Soft tissue complications are clinically relevant problems after osteosynthesis of fractures. The goal is to develop a method for reduction of fibroblast adhesion and proliferation on titanium implant surfaces by plasma polymerisation of the organo-silicon monomer hexamethyldisiloxane (HMDSO). HMDSO...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198807/ https://www.ncbi.nlm.nih.gov/pubmed/25056198 http://dx.doi.org/10.1007/s10856-014-5278-1 |
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author | Kuhn, Sebastian Kroth, Jennifer Ritz, Ulrike Hofmann, Alexander Brendel, Christian Müller, Lars Peter Förch, Renate Rommens, Pol Maria |
author_facet | Kuhn, Sebastian Kroth, Jennifer Ritz, Ulrike Hofmann, Alexander Brendel, Christian Müller, Lars Peter Förch, Renate Rommens, Pol Maria |
author_sort | Kuhn, Sebastian |
collection | PubMed |
description | Soft tissue complications are clinically relevant problems after osteosynthesis of fractures. The goal is to develop a method for reduction of fibroblast adhesion and proliferation on titanium implant surfaces by plasma polymerisation of the organo-silicon monomer hexamethyldisiloxane (HMDSO). HMDSO was deposited under continuous wave conditions in excess oxygen (ppHMDSO surface) and selected samples were further modified with an additional oxygen plasma (ppHMDSO + O(2) surface). Surface characterization was performed by scanning electron microscopy, profilometry, water contact angle measurements, infrared reflection absorption spectroscopy and X-ray photoelectron spectroscopy. In our experimental setup the mechanical properties, roughness and topography of the titanium were preserved, while surface chemistry was drastically changed. Fibroblast proliferation was assessed by alamarBlue assay, cell morphology by confocal microscopy visualization of eGFP-transducted fibroblasts, and cell viability by Annexine V/propidium iodide assay. Both modified surfaces, non-activated hydrophobic ppHMDSO and activated hydrophilic ppHMDSO + O(2) were able to dramatically reduce fibroblast colonization and proliferation compared to standard titanium. However, this effect was more strongly pronounced on the hydrophobic ppHMDSO surface, which caused reduced cell adhesion and prevented proliferation of fibroblasts. The results demonstrate that plasma modifications of titanium using HMDSO are valuable candidates for future developments in anti-adhesive and anti-proliferative coatings for titanium fracture implants. |
format | Online Article Text |
id | pubmed-4198807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-41988072014-10-21 Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces Kuhn, Sebastian Kroth, Jennifer Ritz, Ulrike Hofmann, Alexander Brendel, Christian Müller, Lars Peter Förch, Renate Rommens, Pol Maria J Mater Sci Mater Med Article Soft tissue complications are clinically relevant problems after osteosynthesis of fractures. The goal is to develop a method for reduction of fibroblast adhesion and proliferation on titanium implant surfaces by plasma polymerisation of the organo-silicon monomer hexamethyldisiloxane (HMDSO). HMDSO was deposited under continuous wave conditions in excess oxygen (ppHMDSO surface) and selected samples were further modified with an additional oxygen plasma (ppHMDSO + O(2) surface). Surface characterization was performed by scanning electron microscopy, profilometry, water contact angle measurements, infrared reflection absorption spectroscopy and X-ray photoelectron spectroscopy. In our experimental setup the mechanical properties, roughness and topography of the titanium were preserved, while surface chemistry was drastically changed. Fibroblast proliferation was assessed by alamarBlue assay, cell morphology by confocal microscopy visualization of eGFP-transducted fibroblasts, and cell viability by Annexine V/propidium iodide assay. Both modified surfaces, non-activated hydrophobic ppHMDSO and activated hydrophilic ppHMDSO + O(2) were able to dramatically reduce fibroblast colonization and proliferation compared to standard titanium. However, this effect was more strongly pronounced on the hydrophobic ppHMDSO surface, which caused reduced cell adhesion and prevented proliferation of fibroblasts. The results demonstrate that plasma modifications of titanium using HMDSO are valuable candidates for future developments in anti-adhesive and anti-proliferative coatings for titanium fracture implants. Springer US 2014-07-24 2014 /pmc/articles/PMC4198807/ /pubmed/25056198 http://dx.doi.org/10.1007/s10856-014-5278-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Kuhn, Sebastian Kroth, Jennifer Ritz, Ulrike Hofmann, Alexander Brendel, Christian Müller, Lars Peter Förch, Renate Rommens, Pol Maria Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title | Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title_full | Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title_fullStr | Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title_full_unstemmed | Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title_short | Reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
title_sort | reduced fibroblast adhesion and proliferation on plasma-modified titanium surfaces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198807/ https://www.ncbi.nlm.nih.gov/pubmed/25056198 http://dx.doi.org/10.1007/s10856-014-5278-1 |
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