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In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics

The present study aimed to assess the efficacy of photofunctionalization on commercially available dental implant surfaces in a high-glucose environment. Discs of three commercially available implant surfaces were selected with various nano- and microstructural alterations (Group 1—laser-etched impl...

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Autores principales: Kheur, Supriya, Kheur, Mohit, Madiwal, Vaibhav, Sandhu, Ramandeep, Lakha, Tabrez, Rajwade, Jyutika, Eyüboğlu, Tan Fırat, Özcan, Mutlu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056823/
https://www.ncbi.nlm.nih.gov/pubmed/36976054
http://dx.doi.org/10.3390/jfb14030130
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author Kheur, Supriya
Kheur, Mohit
Madiwal, Vaibhav
Sandhu, Ramandeep
Lakha, Tabrez
Rajwade, Jyutika
Eyüboğlu, Tan Fırat
Özcan, Mutlu
author_facet Kheur, Supriya
Kheur, Mohit
Madiwal, Vaibhav
Sandhu, Ramandeep
Lakha, Tabrez
Rajwade, Jyutika
Eyüboğlu, Tan Fırat
Özcan, Mutlu
author_sort Kheur, Supriya
collection PubMed
description The present study aimed to assess the efficacy of photofunctionalization on commercially available dental implant surfaces in a high-glucose environment. Discs of three commercially available implant surfaces were selected with various nano- and microstructural alterations (Group 1—laser-etched implant surface, Group 2—titanium–zirconium alloy surface, Group 3—air-abraded, large grit, acid-etched surface). They were subjected to photo-functionalization through UV irradiation for 60 and 90 min. X-ray photoelectron spectroscopy (XPS) was used to analyze the implant surface chemical composition before and after photo-functionalization. The growth and bioactivity of MG63 osteoblasts in the presence of photofunctionalized discs was assessed in cell culture medium containing elevated glucose concentration. The normal osteoblast morphology and spreading behavior were assessed under fluorescence and phase-contrast microscope. MTT (3-(4,5 Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and alizarin red assay were performed to assess the osteoblastic cell viability and mineralization efficiency. Following photofunctionalization, all three implant groups exhibited a reduced carbon content, conversion of Ti4+ to Ti3+, increased osteoblastic adhesion, viability, and increased mineralization. The best osteoblastic adhesion in the medium with increased glucose was seen in Group 3. Photofunctionalization altered the implant surface chemistry by reducing the surface carbon content, probably rendering the surfaces more hydrophilic and conducive for osteoblastic adherence and subsequent mineralization in high-glucose environment.
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spelling pubmed-100568232023-03-30 In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics Kheur, Supriya Kheur, Mohit Madiwal, Vaibhav Sandhu, Ramandeep Lakha, Tabrez Rajwade, Jyutika Eyüboğlu, Tan Fırat Özcan, Mutlu J Funct Biomater Article The present study aimed to assess the efficacy of photofunctionalization on commercially available dental implant surfaces in a high-glucose environment. Discs of three commercially available implant surfaces were selected with various nano- and microstructural alterations (Group 1—laser-etched implant surface, Group 2—titanium–zirconium alloy surface, Group 3—air-abraded, large grit, acid-etched surface). They were subjected to photo-functionalization through UV irradiation for 60 and 90 min. X-ray photoelectron spectroscopy (XPS) was used to analyze the implant surface chemical composition before and after photo-functionalization. The growth and bioactivity of MG63 osteoblasts in the presence of photofunctionalized discs was assessed in cell culture medium containing elevated glucose concentration. The normal osteoblast morphology and spreading behavior were assessed under fluorescence and phase-contrast microscope. MTT (3-(4,5 Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and alizarin red assay were performed to assess the osteoblastic cell viability and mineralization efficiency. Following photofunctionalization, all three implant groups exhibited a reduced carbon content, conversion of Ti4+ to Ti3+, increased osteoblastic adhesion, viability, and increased mineralization. The best osteoblastic adhesion in the medium with increased glucose was seen in Group 3. Photofunctionalization altered the implant surface chemistry by reducing the surface carbon content, probably rendering the surfaces more hydrophilic and conducive for osteoblastic adherence and subsequent mineralization in high-glucose environment. MDPI 2023-02-26 /pmc/articles/PMC10056823/ /pubmed/36976054 http://dx.doi.org/10.3390/jfb14030130 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kheur, Supriya
Kheur, Mohit
Madiwal, Vaibhav
Sandhu, Ramandeep
Lakha, Tabrez
Rajwade, Jyutika
Eyüboğlu, Tan Fırat
Özcan, Mutlu
In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title_full In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title_fullStr In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title_full_unstemmed In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title_short In-Vitro Evaluation of Photofunctionalized Implant Surfaces in a High-Glucose Microenvironment Simulating Diabetics
title_sort in-vitro evaluation of photofunctionalized implant surfaces in a high-glucose microenvironment simulating diabetics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056823/
https://www.ncbi.nlm.nih.gov/pubmed/36976054
http://dx.doi.org/10.3390/jfb14030130
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