Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Dental Journal |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402009000400001 |
Resumo: | The aim of this study was to evaluate the trans-enamel and trans-dentinal effects of a 35% hydrogen peroxide (H2O2) bleaching gel on odontoblast-like cells. Enamel/dentin discs obtained from bovine incisors were mounted in artificial pulp chambers (APCs). Three groups were formed: G1- 35% H2O2; G2- 35% H2O2 + halogen light application; G3- control. The treatments were repeated 5 times and the APCs were incubated for 12 h. Then, the extract was collected and applied for 24 h on the cells. Cell metabolism, total protein dosage and cell morphology were evaluated. Cell metabolism decreased by 62.09% and 61.83% in G1 and G2, respectively. The depression of cell metabolism was statistically significant when G1 and G2 were compared to G3. Total protein dosage decreased by 93.13% and 91.80% in G1 and G2, respectively. The cells in G1 and G2 exhibited significant morphological alterations after contact with the extracts. Regardless of halogen light application, the extracts caused significantly more intense cytopathic effects compared to the control group. After 5 consecutive applications of a 35% H2O2 bleaching agent, either catalyzed or not by halogen light, products of gel degradation were capable to diffuse through enamel and dentin causing toxic effects to the cells. |
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Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cellstooth bleachinghydrogen peroxideodontoblastscytotoxicityThe aim of this study was to evaluate the trans-enamel and trans-dentinal effects of a 35% hydrogen peroxide (H2O2) bleaching gel on odontoblast-like cells. Enamel/dentin discs obtained from bovine incisors were mounted in artificial pulp chambers (APCs). Three groups were formed: G1- 35% H2O2; G2- 35% H2O2 + halogen light application; G3- control. The treatments were repeated 5 times and the APCs were incubated for 12 h. Then, the extract was collected and applied for 24 h on the cells. Cell metabolism, total protein dosage and cell morphology were evaluated. Cell metabolism decreased by 62.09% and 61.83% in G1 and G2, respectively. The depression of cell metabolism was statistically significant when G1 and G2 were compared to G3. Total protein dosage decreased by 93.13% and 91.80% in G1 and G2, respectively. The cells in G1 and G2 exhibited significant morphological alterations after contact with the extracts. Regardless of halogen light application, the extracts caused significantly more intense cytopathic effects compared to the control group. After 5 consecutive applications of a 35% H2O2 bleaching agent, either catalyzed or not by halogen light, products of gel degradation were capable to diffuse through enamel and dentin causing toxic effects to the cells.Fundação Odontológica de Ribeirão Preto2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402009000400001Brazilian Dental Journal v.20 n.4 2009reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/S0103-64402009000400001info:eu-repo/semantics/openAccessColdebella,Cármen ReginaRibeiro,Ana Paula DiasSacono,Nancy TomokoTrindade,Flávia ZardoHebling,JosimeriCosta,Carlos Alberto de Souzaeng2009-12-18T00:00:00Zoai:scielo:S0103-64402009000400001Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2009-12-18T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false |
dc.title.none.fl_str_mv |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
title |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
spellingShingle |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells Coldebella,Cármen Regina tooth bleaching hydrogen peroxide odontoblasts cytotoxicity |
title_short |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
title_full |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
title_fullStr |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
title_full_unstemmed |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
title_sort |
Indirect cytotoxicity of a 35% hydrogen peroxide bleaching gel on cultured odontoblast-like cells |
author |
Coldebella,Cármen Regina |
author_facet |
Coldebella,Cármen Regina Ribeiro,Ana Paula Dias Sacono,Nancy Tomoko Trindade,Flávia Zardo Hebling,Josimeri Costa,Carlos Alberto de Souza |
author_role |
author |
author2 |
Ribeiro,Ana Paula Dias Sacono,Nancy Tomoko Trindade,Flávia Zardo Hebling,Josimeri Costa,Carlos Alberto de Souza |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Coldebella,Cármen Regina Ribeiro,Ana Paula Dias Sacono,Nancy Tomoko Trindade,Flávia Zardo Hebling,Josimeri Costa,Carlos Alberto de Souza |
dc.subject.por.fl_str_mv |
tooth bleaching hydrogen peroxide odontoblasts cytotoxicity |
topic |
tooth bleaching hydrogen peroxide odontoblasts cytotoxicity |
description |
The aim of this study was to evaluate the trans-enamel and trans-dentinal effects of a 35% hydrogen peroxide (H2O2) bleaching gel on odontoblast-like cells. Enamel/dentin discs obtained from bovine incisors were mounted in artificial pulp chambers (APCs). Three groups were formed: G1- 35% H2O2; G2- 35% H2O2 + halogen light application; G3- control. The treatments were repeated 5 times and the APCs were incubated for 12 h. Then, the extract was collected and applied for 24 h on the cells. Cell metabolism, total protein dosage and cell morphology were evaluated. Cell metabolism decreased by 62.09% and 61.83% in G1 and G2, respectively. The depression of cell metabolism was statistically significant when G1 and G2 were compared to G3. Total protein dosage decreased by 93.13% and 91.80% in G1 and G2, respectively. The cells in G1 and G2 exhibited significant morphological alterations after contact with the extracts. Regardless of halogen light application, the extracts caused significantly more intense cytopathic effects compared to the control group. After 5 consecutive applications of a 35% H2O2 bleaching agent, either catalyzed or not by halogen light, products of gel degradation were capable to diffuse through enamel and dentin causing toxic effects to the cells. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-01-01 |
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=S0103-64402009000400001 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402009000400001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-64402009000400001 |
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 |
Fundação Odontológica de Ribeirão Preto |
publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
dc.source.none.fl_str_mv |
Brazilian Dental Journal v.20 n.4 2009 reponame:Brazilian Dental Journal instname:Fundação Odontológica de Ribeirão Preto (FUNORP) instacron:FUNORP |
instname_str |
Fundação Odontológica de Ribeirão Preto (FUNORP) |
instacron_str |
FUNORP |
institution |
FUNORP |
reponame_str |
Brazilian Dental Journal |
collection |
Brazilian Dental Journal |
repository.name.fl_str_mv |
Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP) |
repository.mail.fl_str_mv |
bdj@forp.usp.br||sergio@fosjc.unesp.br |
_version_ |
1754204090996359168 |