Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.prosdent.2016.06.001 http://hdl.handle.net/11449/162135 |
Resumo: | Statement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group. |
id |
UNSP_eccd6e2ea995f4dd8142bb8624e7651d |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/162135 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell lineStatement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group.National Council for Scientific and Technological DevelopmentCoordination for the Improvement of Higher Education PersonnelFoundation for Support to Research of the State of Sao Paulo scholarshipSao Paulo State Univ, Aracatuba Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Basic Sci, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Basic Sci, Sao Paulo, BrazilFoundation for Support to Research of the State of Sao Paulo scholarship: 2013/11830-4Elsevier B.V.Universidade Estadual Paulista (Unesp)Freitas da Silva, Emily Vivianne [UNESP]Goiato, Marcelo Coelho [UNESP]Santos, Daniela Micheline dos [UNESP]Bonatto, Liliane da Rocha [UNESP]Balera Brito, Victor Gustavo [UNESP]Penha de Oliveira, Sandra Helena [UNESP]2018-11-26T17:10:32Z2018-11-26T17:10:32Z2016-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article818-823application/pdfhttp://dx.doi.org/10.1016/j.prosdent.2016.06.001Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016.0022-3913http://hdl.handle.net/11449/16213510.1016/j.prosdent.2016.06.001WOS:000387302400018WOS000387302400018.pdf9719883814872582Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Prosthetic Dentistry1,087info:eu-repo/semantics/openAccess2024-09-19T14:51:59Zoai:repositorio.unesp.br:11449/162135Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T14:51:59Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
title |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
spellingShingle |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line Freitas da Silva, Emily Vivianne [UNESP] |
title_short |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
title_full |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
title_fullStr |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
title_full_unstemmed |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
title_sort |
Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line |
author |
Freitas da Silva, Emily Vivianne [UNESP] |
author_facet |
Freitas da Silva, Emily Vivianne [UNESP] Goiato, Marcelo Coelho [UNESP] Santos, Daniela Micheline dos [UNESP] Bonatto, Liliane da Rocha [UNESP] Balera Brito, Victor Gustavo [UNESP] Penha de Oliveira, Sandra Helena [UNESP] |
author_role |
author |
author2 |
Goiato, Marcelo Coelho [UNESP] Santos, Daniela Micheline dos [UNESP] Bonatto, Liliane da Rocha [UNESP] Balera Brito, Victor Gustavo [UNESP] Penha de Oliveira, Sandra Helena [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Freitas da Silva, Emily Vivianne [UNESP] Goiato, Marcelo Coelho [UNESP] Santos, Daniela Micheline dos [UNESP] Bonatto, Liliane da Rocha [UNESP] Balera Brito, Victor Gustavo [UNESP] Penha de Oliveira, Sandra Helena [UNESP] |
description |
Statement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-11-01 2018-11-26T17:10:32Z 2018-11-26T17:10:32Z |
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.prosdent.2016.06.001 Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016. 0022-3913 http://hdl.handle.net/11449/162135 10.1016/j.prosdent.2016.06.001 WOS:000387302400018 WOS000387302400018.pdf 9719883814872582 |
url |
http://dx.doi.org/10.1016/j.prosdent.2016.06.001 http://hdl.handle.net/11449/162135 |
identifier_str_mv |
Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016. 0022-3913 10.1016/j.prosdent.2016.06.001 WOS:000387302400018 WOS000387302400018.pdf 9719883814872582 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Prosthetic Dentistry 1,087 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
818-823 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science 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 |
repositoriounesp@unesp.br |
_version_ |
1813546511036841984 |