Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2019 |
| Outros Autores: | , , , , , , , , |
| Tipo de documento: | Artigo |
| Idioma: | eng |
| Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
| Texto Completo: | https://hdl.handle.net/10316/107144 https://doi.org/10.3390/ma12071184 |
Resumo: | (1) Background: When pulp exposure occurs, reparative dentinogenesis can be induced by direct pulp capping to maintain the vitality and function of the tissue. The aim of this work was to assess the cytotoxicity and bioactivity of three different direct pulp capping materials, calcium hydroxide (Life®), mineral trioxide aggregate (WhiteProRoot®MTA) and calcium silicate (Biodentine™), in an odontoblast-like mouse cell line (MDPC-23). (2) Methods: Metabolic activity was assessed by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test (MTT)assay, viability by the sulforhodamine B (SRB) assay, and the type of death and cell cycle analysis by flow cytometry. Alkaline phosphatase was evaluated by polymerase chain reaction (PCR), and dentin sialoprotein expression was assessed by immunocytochemistry. Mineralization was determined by the Alizarin Red S colorimetric assay and quantified by spectrophotometry. (3) Results: Life® induced a decrease in metabolic activity and viability, which is associated with an increase cell death. WhiteProRoot®MTA and Biodentine™ induced similar effects in cytotoxicity assays, with an increase in the expression of dentin sialoprotein (DSP) and formation of mineralized deposits, especially with Biodentine™. (4) Conclusions: The results of WhiteProRoot®MTA confirm its indication for these therapies, justifying its recognition as the "gold standard". Biodentine™ may be an alternative, since they promote the same cellular response that mineral trioxide aggregate (MTA) does. |
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Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activitybiocompatibilitybiomaterialscytotoxicitydentinogenesisodontoblastpulp capping(1) Background: When pulp exposure occurs, reparative dentinogenesis can be induced by direct pulp capping to maintain the vitality and function of the tissue. The aim of this work was to assess the cytotoxicity and bioactivity of three different direct pulp capping materials, calcium hydroxide (Life®), mineral trioxide aggregate (WhiteProRoot®MTA) and calcium silicate (Biodentine™), in an odontoblast-like mouse cell line (MDPC-23). (2) Methods: Metabolic activity was assessed by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test (MTT)assay, viability by the sulforhodamine B (SRB) assay, and the type of death and cell cycle analysis by flow cytometry. Alkaline phosphatase was evaluated by polymerase chain reaction (PCR), and dentin sialoprotein expression was assessed by immunocytochemistry. Mineralization was determined by the Alizarin Red S colorimetric assay and quantified by spectrophotometry. (3) Results: Life® induced a decrease in metabolic activity and viability, which is associated with an increase cell death. WhiteProRoot®MTA and Biodentine™ induced similar effects in cytotoxicity assays, with an increase in the expression of dentin sialoprotein (DSP) and formation of mineralized deposits, especially with Biodentine™. (4) Conclusions: The results of WhiteProRoot®MTA confirm its indication for these therapies, justifying its recognition as the "gold standard". Biodentine™ may be an alternative, since they promote the same cellular response that mineral trioxide aggregate (MTA) does.GAI 2013 (Faculdade de Medicina da Universidade de Coimbra)MDPI2019-04-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/107144https://hdl.handle.net/10316/107144https://doi.org/10.3390/ma12071184eng1996-194430978943Paula, AnabelaLaranjo, MafaldaMarto, Carlos MiguelAbrantes, Ana MargaridaCasalta-Lopes, JoãoGonçalves, Ana CristinaRibeiro, Ana Bela SarmentoFerreira, Manuel M.Botelho, Maria FilomenaCarrilho, Euniceinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-09-03T16:00:22Zoai:estudogeral.uc.pt:10316/107144Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:57:51.954316Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
| dc.title.none.fl_str_mv |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| title |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| spellingShingle |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity Paula, Anabela biocompatibility biomaterials cytotoxicity dentinogenesis odontoblast pulp capping |
| title_short |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| title_full |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| title_fullStr |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| title_full_unstemmed |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| title_sort |
Biodentine™ Boosts, WhiteProRoot®MTA Increases and Life® Suppresses Odontoblast Activity |
| author |
Paula, Anabela |
| author_facet |
Paula, Anabela Laranjo, Mafalda Marto, Carlos Miguel Abrantes, Ana Margarida Casalta-Lopes, João Gonçalves, Ana Cristina Ribeiro, Ana Bela Sarmento Ferreira, Manuel M. Botelho, Maria Filomena Carrilho, Eunice |
| author_role |
author |
| author2 |
Laranjo, Mafalda Marto, Carlos Miguel Abrantes, Ana Margarida Casalta-Lopes, João Gonçalves, Ana Cristina Ribeiro, Ana Bela Sarmento Ferreira, Manuel M. Botelho, Maria Filomena Carrilho, Eunice |
| author2_role |
author author author author author author author author author |
| dc.contributor.author.fl_str_mv |
Paula, Anabela Laranjo, Mafalda Marto, Carlos Miguel Abrantes, Ana Margarida Casalta-Lopes, João Gonçalves, Ana Cristina Ribeiro, Ana Bela Sarmento Ferreira, Manuel M. Botelho, Maria Filomena Carrilho, Eunice |
| dc.subject.por.fl_str_mv |
biocompatibility biomaterials cytotoxicity dentinogenesis odontoblast pulp capping |
| topic |
biocompatibility biomaterials cytotoxicity dentinogenesis odontoblast pulp capping |
| description |
(1) Background: When pulp exposure occurs, reparative dentinogenesis can be induced by direct pulp capping to maintain the vitality and function of the tissue. The aim of this work was to assess the cytotoxicity and bioactivity of three different direct pulp capping materials, calcium hydroxide (Life®), mineral trioxide aggregate (WhiteProRoot®MTA) and calcium silicate (Biodentine™), in an odontoblast-like mouse cell line (MDPC-23). (2) Methods: Metabolic activity was assessed by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test (MTT)assay, viability by the sulforhodamine B (SRB) assay, and the type of death and cell cycle analysis by flow cytometry. Alkaline phosphatase was evaluated by polymerase chain reaction (PCR), and dentin sialoprotein expression was assessed by immunocytochemistry. Mineralization was determined by the Alizarin Red S colorimetric assay and quantified by spectrophotometry. (3) Results: Life® induced a decrease in metabolic activity and viability, which is associated with an increase cell death. WhiteProRoot®MTA and Biodentine™ induced similar effects in cytotoxicity assays, with an increase in the expression of dentin sialoprotein (DSP) and formation of mineralized deposits, especially with Biodentine™. (4) Conclusions: The results of WhiteProRoot®MTA confirm its indication for these therapies, justifying its recognition as the "gold standard". Biodentine™ may be an alternative, since they promote the same cellular response that mineral trioxide aggregate (MTA) does. |
| publishDate |
2019 |
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2019-04-11 |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
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https://hdl.handle.net/10316/107144 https://hdl.handle.net/10316/107144 https://doi.org/10.3390/ma12071184 |
| url |
https://hdl.handle.net/10316/107144 https://doi.org/10.3390/ma12071184 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
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1996-1944 30978943 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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MDPI |
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MDPI |
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