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Piranha-etched titanium nanostructure reduces biofilm formation in vitro

OBJECTIVES: Nano-modified surfaces for dental implants may improve gingival fibroblast adhesion and antibacterial characteristics through cell-surface interactions. The present study investigated how a nanocavity titanium surface impacts the viability and adhesion of human gingival fibroblasts (HGF-...

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Autores principales: Mukaddam, Khaled, Astasov-Frauenhoffer, Monika, Fasler-Kan, Elizaveta, Ruggiero, Sabrina, Alhawasli, Farah, Kisiel, Marcin, Meyer, Ernst, Köser, Jochen, Bornstein, Michael M., Wagner, Raphael S., Kühl, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560173/
https://www.ncbi.nlm.nih.gov/pubmed/37653076
http://dx.doi.org/10.1007/s00784-023-05235-4
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author Mukaddam, Khaled
Astasov-Frauenhoffer, Monika
Fasler-Kan, Elizaveta
Ruggiero, Sabrina
Alhawasli, Farah
Kisiel, Marcin
Meyer, Ernst
Köser, Jochen
Bornstein, Michael M.
Wagner, Raphael S.
Kühl, Sebastian
author_facet Mukaddam, Khaled
Astasov-Frauenhoffer, Monika
Fasler-Kan, Elizaveta
Ruggiero, Sabrina
Alhawasli, Farah
Kisiel, Marcin
Meyer, Ernst
Köser, Jochen
Bornstein, Michael M.
Wagner, Raphael S.
Kühl, Sebastian
author_sort Mukaddam, Khaled
collection PubMed
description OBJECTIVES: Nano-modified surfaces for dental implants may improve gingival fibroblast adhesion and antibacterial characteristics through cell-surface interactions. The present study investigated how a nanocavity titanium surface impacts the viability and adhesion of human gingival fibroblasts (HGF-1) and compared its response to Porphyromonas gingivalis with those of marketed implant surfaces. MATERIAL AND METHODS: Commercial titanium and zirconia disks, namely, sandblasted and acid-etched titanium (SLA), sandblasted and acid-etched zirconia (ZLA), polished titanium (PT) and polished zirconia (ZrP), and nanostructured disks (NTDs) were tested. Polished titanium disks were etched with a 1:1 combination of 98% H(2)SO(4) and 30% H(2)O(2) (piranha etching) for 5 h at room temperature to produce the NTDs. Atomic force microscopy was used to measure the surface topography, roughness, adhesion force, and work of adhesion. MTT assays and immunofluorescence staining were used to examine cell viability and adhesion after incubation of HGF-1 cells on the disk surfaces. After incubation with P. gingivalis, conventional culture, live/dead staining, and SEM were used to determine the antibacterial properties of NTD, SLA, ZLA, PT, and ZrP. RESULTS: Etching created nanocavities with 10–20-nm edge-to-edge diameters. Chemical etching increased the average surface roughness and decreased the surface adherence, while polishing and flattening of ZrP increased adhesion. However, only the NTDs inhibited biofilm formation and bacterial adherence. The NTDs showed antibacterial effects and P. gingivalis vitality reductions. The HGF-1 cells demonstrated greater viability on the NTDs compared to the controls. CONCLUSION: Nanocavities with 10–20-nm edge-to-edge diameters on titanium disks hindered P. gingivalis adhesion and supported the adhesion of gingival fibroblasts when compared to the surfaces of currently marketed titanium or zirconia dental implants. CLINICAL RELEVANCE: This study prepared an effective antibacterial nanoporous surface, assessed its effects against oral pathogens, and demonstrated that surface characteristics on a nanoscale level influenced oral pathogens and gingival fibroblasts. Clinical trial registration: not applicable
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spelling pubmed-105601732023-10-09 Piranha-etched titanium nanostructure reduces biofilm formation in vitro Mukaddam, Khaled Astasov-Frauenhoffer, Monika Fasler-Kan, Elizaveta Ruggiero, Sabrina Alhawasli, Farah Kisiel, Marcin Meyer, Ernst Köser, Jochen Bornstein, Michael M. Wagner, Raphael S. Kühl, Sebastian Clin Oral Investig Research OBJECTIVES: Nano-modified surfaces for dental implants may improve gingival fibroblast adhesion and antibacterial characteristics through cell-surface interactions. The present study investigated how a nanocavity titanium surface impacts the viability and adhesion of human gingival fibroblasts (HGF-1) and compared its response to Porphyromonas gingivalis with those of marketed implant surfaces. MATERIAL AND METHODS: Commercial titanium and zirconia disks, namely, sandblasted and acid-etched titanium (SLA), sandblasted and acid-etched zirconia (ZLA), polished titanium (PT) and polished zirconia (ZrP), and nanostructured disks (NTDs) were tested. Polished titanium disks were etched with a 1:1 combination of 98% H(2)SO(4) and 30% H(2)O(2) (piranha etching) for 5 h at room temperature to produce the NTDs. Atomic force microscopy was used to measure the surface topography, roughness, adhesion force, and work of adhesion. MTT assays and immunofluorescence staining were used to examine cell viability and adhesion after incubation of HGF-1 cells on the disk surfaces. After incubation with P. gingivalis, conventional culture, live/dead staining, and SEM were used to determine the antibacterial properties of NTD, SLA, ZLA, PT, and ZrP. RESULTS: Etching created nanocavities with 10–20-nm edge-to-edge diameters. Chemical etching increased the average surface roughness and decreased the surface adherence, while polishing and flattening of ZrP increased adhesion. However, only the NTDs inhibited biofilm formation and bacterial adherence. The NTDs showed antibacterial effects and P. gingivalis vitality reductions. The HGF-1 cells demonstrated greater viability on the NTDs compared to the controls. CONCLUSION: Nanocavities with 10–20-nm edge-to-edge diameters on titanium disks hindered P. gingivalis adhesion and supported the adhesion of gingival fibroblasts when compared to the surfaces of currently marketed titanium or zirconia dental implants. CLINICAL RELEVANCE: This study prepared an effective antibacterial nanoporous surface, assessed its effects against oral pathogens, and demonstrated that surface characteristics on a nanoscale level influenced oral pathogens and gingival fibroblasts. Clinical trial registration: not applicable Springer Berlin Heidelberg 2023-08-31 2023 /pmc/articles/PMC10560173/ /pubmed/37653076 http://dx.doi.org/10.1007/s00784-023-05235-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Mukaddam, Khaled
Astasov-Frauenhoffer, Monika
Fasler-Kan, Elizaveta
Ruggiero, Sabrina
Alhawasli, Farah
Kisiel, Marcin
Meyer, Ernst
Köser, Jochen
Bornstein, Michael M.
Wagner, Raphael S.
Kühl, Sebastian
Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title_full Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title_fullStr Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title_full_unstemmed Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title_short Piranha-etched titanium nanostructure reduces biofilm formation in vitro
title_sort piranha-etched titanium nanostructure reduces biofilm formation in vitro
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560173/
https://www.ncbi.nlm.nih.gov/pubmed/37653076
http://dx.doi.org/10.1007/s00784-023-05235-4
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