Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages

Detalhes bibliográficos
Autor(a) principal: Lima Chaves, Carolina de Andrade [UNESP]
Data de Publicação: 2014
Outros Autores: Souza Costa, Carlos Alberto de [UNESP], Vergani, Carlos Eduardo [UNESP], Chaves de Souza, Pedro Paulo [UNESP], Machado, Ana Lucia [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1155/2014/840613
http://hdl.handle.net/11449/117242
Resumo: The effects of six soft liners (Ufi Gel P (UG), Sofreliner S (SR), Durabase Soft (D), Trusoft (T), Coe Comfort (CC), and Softone (ST)) on L929, HaCat, and RAW 264.7 cells were investigated. Eluates (24 and 48 h) from the materials were applied on the cells and the viability, type of cell death, and morphology were evaluated. Cells were also seeded on the specimens' surfaces (direct contact) and incubated (24 or 48 h), and viability was analyzed. Controls were cells in culture medium without eluates or specimens. For cell viability, no significant differences were found among materials or between extraction periods, and the liners were noncytotoxic or slightly cytotoxic. Morphology of RAW 264.7 cells was altered by the 24 h eluates from CC and D and the 48 h eluates from SR, CC, and D. The 24 and 48 h eluates from all materials (except T) increased the percentages of L929 necrotic cells. For direct contact tests, the lowest cytotoxicity was observed for UG and SR. Although eluates did not reduce viability, morphology alterations and increase in necrosis were seen. Moreover, in the direct contact, effects on viability were more pronounced, particularly for D, T, CC and ST. Thus, the use of UG and SR might reduce the risk of adverse effects.
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spelling Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 MacrophagesThe effects of six soft liners (Ufi Gel P (UG), Sofreliner S (SR), Durabase Soft (D), Trusoft (T), Coe Comfort (CC), and Softone (ST)) on L929, HaCat, and RAW 264.7 cells were investigated. Eluates (24 and 48 h) from the materials were applied on the cells and the viability, type of cell death, and morphology were evaluated. Cells were also seeded on the specimens' surfaces (direct contact) and incubated (24 or 48 h), and viability was analyzed. Controls were cells in culture medium without eluates or specimens. For cell viability, no significant differences were found among materials or between extraction periods, and the liners were noncytotoxic or slightly cytotoxic. Morphology of RAW 264.7 cells was altered by the 24 h eluates from CC and D and the 48 h eluates from SR, CC, and D. The 24 and 48 h eluates from all materials (except T) increased the percentages of L929 necrotic cells. For direct contact tests, the lowest cytotoxicity was observed for UG and SR. Although eluates did not reduce viability, morphology alterations and increase in necrosis were seen. Moreover, in the direct contact, effects on viability were more pronounced, particularly for D, T, CC and ST. Thus, the use of UG and SR might reduce the risk of adverse effects.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação para o Desenvolvimento da UNESP (FUNDUNESP)Univ Estadual Paulista, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, UNESP, BR-14801903 Araraquara, SP, BrazilUniv Estadual Paulista, Araraquara Dent Sch, Dept Physiol & Pathol, UNESP, BR-14801903 Araraquara, SP, BrazilUniv Estadual Paulista, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, UNESP, BR-14801903 Araraquara, SP, BrazilUniv Estadual Paulista, Araraquara Dent Sch, Dept Physiol & Pathol, UNESP, BR-14801903 Araraquara, SP, BrazilFAPESP: 10/08750-0FAPESP: 10/11764-3FAPESP: 12/07994-9CNPq: 302543/2010-4Hindawi Publishing CorporationUniversidade Estadual Paulista (Unesp)Lima Chaves, Carolina de Andrade [UNESP]Souza Costa, Carlos Alberto de [UNESP]Vergani, Carlos Eduardo [UNESP]Chaves de Souza, Pedro Paulo [UNESP]Machado, Ana Lucia [UNESP]2015-03-18T15:55:37Z2015-03-18T15:55:37Z2014-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article14application/epub+zipapplication/pdfhttp://dx.doi.org/10.1155/2014/840613Biomed Research International. New York: Hindawi Publishing Corporation, 14 p., 2014.2314-6133http://hdl.handle.net/11449/11724210.1155/2014/840613WOS:000346014700001WOS000346014700001.pdfWOS000346014700001.epub4517484241515548300313052242782080002487818425870000-0002-7375-4714Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiomed Research International2.5830,935info:eu-repo/semantics/openAccess2023-12-01T06:13:31Zoai:repositorio.unesp.br:11449/117242Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-01T06:13:31Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
title Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
spellingShingle Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
Lima Chaves, Carolina de Andrade [UNESP]
title_short Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
title_full Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
title_fullStr Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
title_full_unstemmed Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
title_sort Effects of Soft Denture Liners on L929 Fibroblasts, HaCaT Keratinocytes, and RAW 264.7 Macrophages
author Lima Chaves, Carolina de Andrade [UNESP]
author_facet Lima Chaves, Carolina de Andrade [UNESP]
Souza Costa, Carlos Alberto de [UNESP]
Vergani, Carlos Eduardo [UNESP]
Chaves de Souza, Pedro Paulo [UNESP]
Machado, Ana Lucia [UNESP]
author_role author
author2 Souza Costa, Carlos Alberto de [UNESP]
Vergani, Carlos Eduardo [UNESP]
Chaves de Souza, Pedro Paulo [UNESP]
Machado, Ana Lucia [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Lima Chaves, Carolina de Andrade [UNESP]
Souza Costa, Carlos Alberto de [UNESP]
Vergani, Carlos Eduardo [UNESP]
Chaves de Souza, Pedro Paulo [UNESP]
Machado, Ana Lucia [UNESP]
description The effects of six soft liners (Ufi Gel P (UG), Sofreliner S (SR), Durabase Soft (D), Trusoft (T), Coe Comfort (CC), and Softone (ST)) on L929, HaCat, and RAW 264.7 cells were investigated. Eluates (24 and 48 h) from the materials were applied on the cells and the viability, type of cell death, and morphology were evaluated. Cells were also seeded on the specimens' surfaces (direct contact) and incubated (24 or 48 h), and viability was analyzed. Controls were cells in culture medium without eluates or specimens. For cell viability, no significant differences were found among materials or between extraction periods, and the liners were noncytotoxic or slightly cytotoxic. Morphology of RAW 264.7 cells was altered by the 24 h eluates from CC and D and the 48 h eluates from SR, CC, and D. The 24 and 48 h eluates from all materials (except T) increased the percentages of L929 necrotic cells. For direct contact tests, the lowest cytotoxicity was observed for UG and SR. Although eluates did not reduce viability, morphology alterations and increase in necrosis were seen. Moreover, in the direct contact, effects on viability were more pronounced, particularly for D, T, CC and ST. Thus, the use of UG and SR might reduce the risk of adverse effects.
publishDate 2014
dc.date.none.fl_str_mv 2014-01-01
2015-03-18T15:55:37Z
2015-03-18T15:55:37Z
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format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1155/2014/840613
Biomed Research International. New York: Hindawi Publishing Corporation, 14 p., 2014.
2314-6133
http://hdl.handle.net/11449/117242
10.1155/2014/840613
WOS:000346014700001
WOS000346014700001.pdf
WOS000346014700001.epub
4517484241515548
3003130522427820
8000248781842587
0000-0002-7375-4714
url http://dx.doi.org/10.1155/2014/840613
http://hdl.handle.net/11449/117242
identifier_str_mv Biomed Research International. New York: Hindawi Publishing Corporation, 14 p., 2014.
2314-6133
10.1155/2014/840613
WOS:000346014700001
WOS000346014700001.pdf
WOS000346014700001.epub
4517484241515548
3003130522427820
8000248781842587
0000-0002-7375-4714
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biomed Research International
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dc.publisher.none.fl_str_mv Hindawi Publishing Corporation
publisher.none.fl_str_mv Hindawi Publishing Corporation
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