Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.tiv.2021.105211 http://hdl.handle.net/11449/229110 |
Resumo: | The study evaluated the influence of cycles and methods of an ocular prosthesis resin on cytotoxicity toward human conjunctival cells. Resins were polymerized by water bath (WB, 74 °C or 100 °C for 30 min to 9 h), microwave (MW, 1200 W, 3 to 14 min and 30 s at 0 to 720 W), or autopolymerization (AP, room temperature for 20 min ± 60 °C for 30 min). Degree of conversion (DC), cytotoxicity, level of inflammatory mediators, gene expression of different markers, and apoptosis were evaluated. Data were submitted to ANOVA and Tukey test (p < 0.05). WB with longer processing time at higher temperature had highest DC (85.6%) and higher TGF β1-gene expression (1.39); long cycle low power MW showed lowest DC (69.6%), lower cell proliferation (85.4%, MTT), and large IL-2 release (39,297 ng/mL). AP with additional processing time showed lower cell proliferation (75.3%, Alamar Blue), and AP polymerized at room temperature showed higher CASP 9-gene expression (1.21). AP methods showed higher IL-6 release (>277 pg/mL). Short cycle medium power MW had higher IL-23 release (534.2 pg/mL). MW (long and short cycles) and AP polymerizations have triggered a more intense inflammatory response. Among methods recommended by the manufacturer, WB showed high DC and less cytotoxicity. |
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Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro studyCellular immune responseCytotoxicityMethyl methacrylateOcular prosthesisThe study evaluated the influence of cycles and methods of an ocular prosthesis resin on cytotoxicity toward human conjunctival cells. Resins were polymerized by water bath (WB, 74 °C or 100 °C for 30 min to 9 h), microwave (MW, 1200 W, 3 to 14 min and 30 s at 0 to 720 W), or autopolymerization (AP, room temperature for 20 min ± 60 °C for 30 min). Degree of conversion (DC), cytotoxicity, level of inflammatory mediators, gene expression of different markers, and apoptosis were evaluated. Data were submitted to ANOVA and Tukey test (p < 0.05). WB with longer processing time at higher temperature had highest DC (85.6%) and higher TGF β1-gene expression (1.39); long cycle low power MW showed lowest DC (69.6%), lower cell proliferation (85.4%, MTT), and large IL-2 release (39,297 ng/mL). AP with additional processing time showed lower cell proliferation (75.3%, Alamar Blue), and AP polymerized at room temperature showed higher CASP 9-gene expression (1.21). AP methods showed higher IL-6 release (>277 pg/mL). Short cycle medium power MW had higher IL-23 release (534.2 pg/mL). MW (long and short cycles) and AP polymerizations have triggered a more intense inflammatory response. Among methods recommended by the manufacturer, WB showed high DC and less cytotoxicity.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Department of Dental Materials and Prosthodontics Aracatuba Dental School Sao Paulo State University (UNESP)Department of Dental Materials and Prosthodontics Aracatuba Dental School UNESPOral Oncology Center São Paulo State University (Unesp) School of Dentistry, 1193 José Bonifácio StFaculty of Dentistry University of TorontoInstitute of Biomedical Engineering University of TorontoDepartment of Basic Sciences Aracatuba Dental School UNESPDepartment of Dental Materials and Prosthodontics Aracatuba Dental School Sao Paulo State University (UNESP)Department of Dental Materials and Prosthodontics Aracatuba Dental School UNESPOral Oncology Center São Paulo State University (Unesp) School of Dentistry, 1193 José Bonifácio StDepartment of Basic Sciences Aracatuba Dental School UNESPUniversidade Estadual Paulista (UNESP)University of Torontoda Silva, Emily Vivianne Freitas [UNESP]Goiato, Marcelo Coelho [UNESP]Bitencourt, Sandro Basso [UNESP]Finer, YoavBrito, Victor Gustavo BaleraTakamiya, Aline Satie [UNESP]de Oliveira, Sandra Helena Penha [UNESP]dos Santos, Daniela Micheline [UNESP]2022-04-29T08:30:34Z2022-04-29T08:30:34Z2021-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.tiv.2021.105211Toxicology in Vitro, v. 76.1879-31770887-2333http://hdl.handle.net/11449/22911010.1016/j.tiv.2021.1052112-s2.0-85109502793Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxicology in Vitroinfo:eu-repo/semantics/openAccess2022-04-29T08:30:34Zoai:repositorio.unesp.br:11449/229110Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T08:30:34Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
title |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
spellingShingle |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study da Silva, Emily Vivianne Freitas [UNESP] Cellular immune response Cytotoxicity Methyl methacrylate Ocular prosthesis |
title_short |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
title_full |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
title_fullStr |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
title_full_unstemmed |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
title_sort |
Effect of processing methods on the cytotoxicity of methyl methacrylate-based ocular prostheses: An in vitro study |
author |
da Silva, Emily Vivianne Freitas [UNESP] |
author_facet |
da Silva, Emily Vivianne Freitas [UNESP] Goiato, Marcelo Coelho [UNESP] Bitencourt, Sandro Basso [UNESP] Finer, Yoav Brito, Victor Gustavo Balera Takamiya, Aline Satie [UNESP] de Oliveira, Sandra Helena Penha [UNESP] dos Santos, Daniela Micheline [UNESP] |
author_role |
author |
author2 |
Goiato, Marcelo Coelho [UNESP] Bitencourt, Sandro Basso [UNESP] Finer, Yoav Brito, Victor Gustavo Balera Takamiya, Aline Satie [UNESP] de Oliveira, Sandra Helena Penha [UNESP] dos Santos, Daniela Micheline [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) University of Toronto |
dc.contributor.author.fl_str_mv |
da Silva, Emily Vivianne Freitas [UNESP] Goiato, Marcelo Coelho [UNESP] Bitencourt, Sandro Basso [UNESP] Finer, Yoav Brito, Victor Gustavo Balera Takamiya, Aline Satie [UNESP] de Oliveira, Sandra Helena Penha [UNESP] dos Santos, Daniela Micheline [UNESP] |
dc.subject.por.fl_str_mv |
Cellular immune response Cytotoxicity Methyl methacrylate Ocular prosthesis |
topic |
Cellular immune response Cytotoxicity Methyl methacrylate Ocular prosthesis |
description |
The study evaluated the influence of cycles and methods of an ocular prosthesis resin on cytotoxicity toward human conjunctival cells. Resins were polymerized by water bath (WB, 74 °C or 100 °C for 30 min to 9 h), microwave (MW, 1200 W, 3 to 14 min and 30 s at 0 to 720 W), or autopolymerization (AP, room temperature for 20 min ± 60 °C for 30 min). Degree of conversion (DC), cytotoxicity, level of inflammatory mediators, gene expression of different markers, and apoptosis were evaluated. Data were submitted to ANOVA and Tukey test (p < 0.05). WB with longer processing time at higher temperature had highest DC (85.6%) and higher TGF β1-gene expression (1.39); long cycle low power MW showed lowest DC (69.6%), lower cell proliferation (85.4%, MTT), and large IL-2 release (39,297 ng/mL). AP with additional processing time showed lower cell proliferation (75.3%, Alamar Blue), and AP polymerized at room temperature showed higher CASP 9-gene expression (1.21). AP methods showed higher IL-6 release (>277 pg/mL). Short cycle medium power MW had higher IL-23 release (534.2 pg/mL). MW (long and short cycles) and AP polymerizations have triggered a more intense inflammatory response. Among methods recommended by the manufacturer, WB showed high DC and less cytotoxicity. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-10-01 2022-04-29T08:30:34Z 2022-04-29T08:30:34Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.tiv.2021.105211 Toxicology in Vitro, v. 76. 1879-3177 0887-2333 http://hdl.handle.net/11449/229110 10.1016/j.tiv.2021.105211 2-s2.0-85109502793 |
url |
http://dx.doi.org/10.1016/j.tiv.2021.105211 http://hdl.handle.net/11449/229110 |
identifier_str_mv |
Toxicology in Vitro, v. 76. 1879-3177 0887-2333 10.1016/j.tiv.2021.105211 2-s2.0-85109502793 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Toxicology in Vitro |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1792961684496711680 |