Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of applied oral science (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000600554 |
Resumo: | Objective Mineral Trioxide Aggregate (MTA) is composed of Portland Cement (PC) and bismuth oxide (BO). Replacing BO for niobium oxide (NbO) microparticles (Nbµ) or nanoparticles (Nbη) may improve radiopacity and bioactivity. The aim of this study was to evaluate the radiopacity and cytotoxicity of the materials: 1) PC; 2) White MTA; 3) PC+30% Nbµ; 4) PC+30% Nbη. Material and Methods For the radiopacity test, specimens of the different materials were radiographed along an aluminum step-wedge. For cell culture assays, Saos-2 osteoblastic-cells (ATCC HTB-85) were used. Cell viability was evaluated through MTT assay, and bioactivity was assessed by alkaline phosphatase activity assay. Results The results demonstrated higher radiopacity for MTA, followed by Nbµ and Nbη, which had similar values. Cell culture analysis showed that PC and PC+NbO associations promoted greater cell viability than MTA. Conclusions It was concluded that the combination of PC+NbO is a potential alternative for composition of MTA. |
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Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticlesSilicate cementNiobiumNanotechnology Objective Mineral Trioxide Aggregate (MTA) is composed of Portland Cement (PC) and bismuth oxide (BO). Replacing BO for niobium oxide (NbO) microparticles (Nbµ) or nanoparticles (Nbη) may improve radiopacity and bioactivity. The aim of this study was to evaluate the radiopacity and cytotoxicity of the materials: 1) PC; 2) White MTA; 3) PC+30% Nbµ; 4) PC+30% Nbη. Material and Methods For the radiopacity test, specimens of the different materials were radiographed along an aluminum step-wedge. For cell culture assays, Saos-2 osteoblastic-cells (ATCC HTB-85) were used. Cell viability was evaluated through MTT assay, and bioactivity was assessed by alkaline phosphatase activity assay. Results The results demonstrated higher radiopacity for MTA, followed by Nbµ and Nbη, which had similar values. Cell culture analysis showed that PC and PC+NbO associations promoted greater cell viability than MTA. Conclusions It was concluded that the combination of PC+NbO is a potential alternative for composition of MTA. Faculdade De Odontologia De Bauru - USP2014-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000600554Journal of Applied Oral Science v.22 n.6 2014reponame:Journal of applied oral science (Online)instname:Universidade de São Paulo (USP)instacron:USP10.1590/1678-775720140209info:eu-repo/semantics/openAccessMESTIERI,Leticia BoldrinTANOMARU-FILHO,MárioGOMES-CORNÉLIO,Ana LiviaSALLES,Loise PedrosaBERNARDI,Maria Inês BassoGUERREIRO-TANOMARU,Juliane Mariaeng2014-12-18T00:00:00Zoai:scielo:S1678-77572014000600554Revistahttp://www.scielo.br/jaosPUBhttps://old.scielo.br/oai/scielo-oai.php||jaos@usp.br1678-77651678-7757opendoar:2014-12-18T00:00Journal of applied oral science (Online) - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
title |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
spellingShingle |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles MESTIERI,Leticia Boldrin Silicate cement Niobium Nanotechnology |
title_short |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
title_full |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
title_fullStr |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
title_full_unstemmed |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
title_sort |
Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles |
author |
MESTIERI,Leticia Boldrin |
author_facet |
MESTIERI,Leticia Boldrin TANOMARU-FILHO,Mário GOMES-CORNÉLIO,Ana Livia SALLES,Loise Pedrosa BERNARDI,Maria Inês Basso GUERREIRO-TANOMARU,Juliane Maria |
author_role |
author |
author2 |
TANOMARU-FILHO,Mário GOMES-CORNÉLIO,Ana Livia SALLES,Loise Pedrosa BERNARDI,Maria Inês Basso GUERREIRO-TANOMARU,Juliane Maria |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
MESTIERI,Leticia Boldrin TANOMARU-FILHO,Mário GOMES-CORNÉLIO,Ana Livia SALLES,Loise Pedrosa BERNARDI,Maria Inês Basso GUERREIRO-TANOMARU,Juliane Maria |
dc.subject.por.fl_str_mv |
Silicate cement Niobium Nanotechnology |
topic |
Silicate cement Niobium Nanotechnology |
description |
Objective Mineral Trioxide Aggregate (MTA) is composed of Portland Cement (PC) and bismuth oxide (BO). Replacing BO for niobium oxide (NbO) microparticles (Nbµ) or nanoparticles (Nbη) may improve radiopacity and bioactivity. The aim of this study was to evaluate the radiopacity and cytotoxicity of the materials: 1) PC; 2) White MTA; 3) PC+30% Nbµ; 4) PC+30% Nbη. Material and Methods For the radiopacity test, specimens of the different materials were radiographed along an aluminum step-wedge. For cell culture assays, Saos-2 osteoblastic-cells (ATCC HTB-85) were used. Cell viability was evaluated through MTT assay, and bioactivity was assessed by alkaline phosphatase activity assay. Results The results demonstrated higher radiopacity for MTA, followed by Nbµ and Nbη, which had similar values. Cell culture analysis showed that PC and PC+NbO associations promoted greater cell viability than MTA. Conclusions It was concluded that the combination of PC+NbO is a potential alternative for composition of MTA. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000600554 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000600554 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1678-775720140209 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Faculdade De Odontologia De Bauru - USP |
publisher.none.fl_str_mv |
Faculdade De Odontologia De Bauru - USP |
dc.source.none.fl_str_mv |
Journal of Applied Oral Science v.22 n.6 2014 reponame:Journal of applied oral science (Online) instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Journal of applied oral science (Online) |
collection |
Journal of applied oral science (Online) |
repository.name.fl_str_mv |
Journal of applied oral science (Online) - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||jaos@usp.br |
_version_ |
1748936438185984000 |