Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells

Abstract: The study characterizes dental implant surfaces treated with phosphoric acid to assess the effects of acid treatment on blood cells and correlate them with cytokine levels. The implant surfaces examined were divided into untreated metal surface (US; n = 50), metal surface treated with phos...

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Main Authors: Fernando Luzía França, Adenilda Cristina Honorio-França, Mariana Silva Honorio, Fabiana Helen da Silva, Mahmi Fujimori, Eduardo Luzía França, Fernando Gabriel da Silva Araújo
Format: Article
Language:English
Published: Sociedade Brasileira de Pesquisa Odontológica
Series:Brazilian Oral Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242019000100230&lng=en&tlng=en
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spelling doaj-ea569fdd967444dcb5dfc798749608a22020-11-25T01:17:09ZengSociedade Brasileira de Pesquisa Odontológica Brazilian Oral Research1807-310733010.1590/1807-3107bor-2019.vol33.0040S1806-83242019000100230Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cellsFernando Luzía FrançaAdenilda Cristina Honorio-FrançaMariana Silva HonorioFabiana Helen da SilvaMahmi FujimoriEduardo Luzía FrançaFernando Gabriel da Silva AraújoAbstract: The study characterizes dental implant surfaces treated with phosphoric acid to assess the effects of acid treatment on blood cells and correlate them with cytokine levels. The implant surfaces examined were divided into untreated metal surface (US; n = 50), metal surface treated with phosphoric acid (ATS; n = 50) and cement surface (CS; n = 50) groups. The samples were characterized by scanning electron microscopy (SEM) and rheometry. The implants were incubated with human blood mononuclear cells for 24 h, with surface rinsing in the ATS treatment. Cell viability was determined by colorimetric methods and cytokines in the culture supernatant were quantified using flow cytometry. In the ATS group, the surface porosity and contact surface were increased and plaques were observed on the surface. The blood flow and viscosity curves were similar among the treatments, and the high cell viability rates indicate the biocompatibility of the materials used. An increase in the levels of IL-2, IL-4, IL-6, IL-10 and TNF-α was observed in the ATS and CS groups. There were positive correlations between IL-10 and IL-2 levels and between IL-10 and IL-4 levels in the culture supernatant of the ATS group. The results suggest that implant surface treatment with phosphoric acid activates the production of inflammatory cytokines. The increased cytokine levels can modulate the immune response, thereby improving biofunctional processes and promoting the success of dental implants.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242019000100230&lng=en&tlng=enDental ImplantationPhosphoric AcidsCytokinesRheology
collection DOAJ
language English
format Article
sources DOAJ
author Fernando Luzía França
Adenilda Cristina Honorio-França
Mariana Silva Honorio
Fabiana Helen da Silva
Mahmi Fujimori
Eduardo Luzía França
Fernando Gabriel da Silva Araújo
spellingShingle Fernando Luzía França
Adenilda Cristina Honorio-França
Mariana Silva Honorio
Fabiana Helen da Silva
Mahmi Fujimori
Eduardo Luzía França
Fernando Gabriel da Silva Araújo
Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
Brazilian Oral Research
Dental Implantation
Phosphoric Acids
Cytokines
Rheology
author_facet Fernando Luzía França
Adenilda Cristina Honorio-França
Mariana Silva Honorio
Fabiana Helen da Silva
Mahmi Fujimori
Eduardo Luzía França
Fernando Gabriel da Silva Araújo
author_sort Fernando Luzía França
title Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
title_short Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
title_full Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
title_fullStr Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
title_full_unstemmed Dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood MN cells
title_sort dental implant surfaces treated with phosphoric acid can modulate cytokine production by blood mn cells
publisher Sociedade Brasileira de Pesquisa Odontológica
series Brazilian Oral Research
issn 1807-3107
description Abstract: The study characterizes dental implant surfaces treated with phosphoric acid to assess the effects of acid treatment on blood cells and correlate them with cytokine levels. The implant surfaces examined were divided into untreated metal surface (US; n = 50), metal surface treated with phosphoric acid (ATS; n = 50) and cement surface (CS; n = 50) groups. The samples were characterized by scanning electron microscopy (SEM) and rheometry. The implants were incubated with human blood mononuclear cells for 24 h, with surface rinsing in the ATS treatment. Cell viability was determined by colorimetric methods and cytokines in the culture supernatant were quantified using flow cytometry. In the ATS group, the surface porosity and contact surface were increased and plaques were observed on the surface. The blood flow and viscosity curves were similar among the treatments, and the high cell viability rates indicate the biocompatibility of the materials used. An increase in the levels of IL-2, IL-4, IL-6, IL-10 and TNF-α was observed in the ATS and CS groups. There were positive correlations between IL-10 and IL-2 levels and between IL-10 and IL-4 levels in the culture supernatant of the ATS group. The results suggest that implant surface treatment with phosphoric acid activates the production of inflammatory cytokines. The increased cytokine levels can modulate the immune response, thereby improving biofunctional processes and promoting the success of dental implants.
topic Dental Implantation
Phosphoric Acids
Cytokines
Rheology
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242019000100230&lng=en&tlng=en
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