Bonefill® block as alternative for bone substitute: A toxicological evaluation

Detalhes bibliográficos
Autor(a) principal: Melchior, Karine [UNESP]
Data de Publicação: 2018
Outros Autores: Saska, Sybele [UNESP], Coelho, Fernanda [UNESP], Scarel-Caminaga, Raquel Mantuaneli [UNESP], Capote, Ticiana Sidorenko de Oliveira [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/s2175-97902018000217438
http://hdl.handle.net/11449/180070
Resumo: Bone substitutes based on hydroxyapatite (HA) and Bonefill® (BO-inorganic bovine bone) associated with poly(lactic-co-glycolic acid) (PLGA) (HA/PLGA and BO/PLGA) were evaluated concerning cytotoxicity, genotoxicity and mutagenicity as potential candidates for bone repair. The materials were developed and provided by Bionnovation Biomedical Products Ltda. Eluates from these bone substitutes were prepared for toxicity evaluations using eukaryotic cell cultures. HA/PLGA was used as a comparison for Bonefill®. Cell viability was evaluated by XTT assay and surviving fraction was calculated for clonogenic survival. Additionally, tail moment was used to assess genotoxicity (comet assay). The frequencies of binucleated cells with micronucleus (FBMN), micronucleus (FMN), nucleoplasmic bridges (NPBs), and nuclear buds (NBUDs) were analysed by cytokinesis-block micronucleus assay (CBMN assay). Results showed no statistical difference in cell viability compared with negative control (NC) The eluates did not promote delayed cytotoxicity whereas the surviving fraction rate for cultured cells was similar to NC. Furthermore, no genotoxicity or mutagenicity effects were observed for cultured cells with the Bonefill/PLGA and HA/PLGA eluates. In conclusion, the negative cytotoxicity, genotoxicity and mutagenicity results indicate that these bone substitutes presented interesting preliminary results as potential biomaterials for bone repair.
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spelling Bonefill® block as alternative for bone substitute: A toxicological evaluationBiomaterials/evaluationBone regenerationBonefill®/toxicityHydroxyapatiteBone substitutes based on hydroxyapatite (HA) and Bonefill® (BO-inorganic bovine bone) associated with poly(lactic-co-glycolic acid) (PLGA) (HA/PLGA and BO/PLGA) were evaluated concerning cytotoxicity, genotoxicity and mutagenicity as potential candidates for bone repair. The materials were developed and provided by Bionnovation Biomedical Products Ltda. Eluates from these bone substitutes were prepared for toxicity evaluations using eukaryotic cell cultures. HA/PLGA was used as a comparison for Bonefill®. Cell viability was evaluated by XTT assay and surviving fraction was calculated for clonogenic survival. Additionally, tail moment was used to assess genotoxicity (comet assay). The frequencies of binucleated cells with micronucleus (FBMN), micronucleus (FMN), nucleoplasmic bridges (NPBs), and nuclear buds (NBUDs) were analysed by cytokinesis-block micronucleus assay (CBMN assay). Results showed no statistical difference in cell viability compared with negative control (NC) The eluates did not promote delayed cytotoxicity whereas the surviving fraction rate for cultured cells was similar to NC. Furthermore, no genotoxicity or mutagenicity effects were observed for cultured cells with the Bonefill/PLGA and HA/PLGA eluates. In conclusion, the negative cytotoxicity, genotoxicity and mutagenicity results indicate that these bone substitutes presented interesting preliminary results as potential biomaterials for bone repair.São Paulo State University (UNESP) School of Pharmaceutical SciencesSão Paulo State University (UNESP) School of DentistrySão Paulo State University (UNESP) School of Pharmaceutical SciencesSão Paulo State University (UNESP) School of DentistryUniversidade Estadual Paulista (Unesp)Melchior, Karine [UNESP]Saska, Sybele [UNESP]Coelho, Fernanda [UNESP]Scarel-Caminaga, Raquel Mantuaneli [UNESP]Capote, Ticiana Sidorenko de Oliveira [UNESP]2018-12-11T17:37:53Z2018-12-11T17:37:53Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1590/s2175-97902018000217438Brazilian Journal of Pharmaceutical Sciences, v. 54, n. 2, 2018.2175-97901984-8250http://hdl.handle.net/11449/18007010.1590/s2175-97902018000217438S1984-825020180002006112-s2.0-85050856017S1984-82502018000200611.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrazilian Journal of Pharmaceutical Sciences0,2140,214info:eu-repo/semantics/openAccess2024-09-27T15:15:10Zoai:repositorio.unesp.br:11449/180070Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T15:15:10Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Bonefill® block as alternative for bone substitute: A toxicological evaluation
title Bonefill® block as alternative for bone substitute: A toxicological evaluation
spellingShingle Bonefill® block as alternative for bone substitute: A toxicological evaluation
Melchior, Karine [UNESP]
Biomaterials/evaluation
Bone regeneration
Bonefill®/toxicity
Hydroxyapatite
title_short Bonefill® block as alternative for bone substitute: A toxicological evaluation
title_full Bonefill® block as alternative for bone substitute: A toxicological evaluation
title_fullStr Bonefill® block as alternative for bone substitute: A toxicological evaluation
title_full_unstemmed Bonefill® block as alternative for bone substitute: A toxicological evaluation
title_sort Bonefill® block as alternative for bone substitute: A toxicological evaluation
author Melchior, Karine [UNESP]
author_facet Melchior, Karine [UNESP]
Saska, Sybele [UNESP]
Coelho, Fernanda [UNESP]
Scarel-Caminaga, Raquel Mantuaneli [UNESP]
Capote, Ticiana Sidorenko de Oliveira [UNESP]
author_role author
author2 Saska, Sybele [UNESP]
Coelho, Fernanda [UNESP]
Scarel-Caminaga, Raquel Mantuaneli [UNESP]
Capote, Ticiana Sidorenko de Oliveira [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Melchior, Karine [UNESP]
Saska, Sybele [UNESP]
Coelho, Fernanda [UNESP]
Scarel-Caminaga, Raquel Mantuaneli [UNESP]
Capote, Ticiana Sidorenko de Oliveira [UNESP]
dc.subject.por.fl_str_mv Biomaterials/evaluation
Bone regeneration
Bonefill®/toxicity
Hydroxyapatite
topic Biomaterials/evaluation
Bone regeneration
Bonefill®/toxicity
Hydroxyapatite
description Bone substitutes based on hydroxyapatite (HA) and Bonefill® (BO-inorganic bovine bone) associated with poly(lactic-co-glycolic acid) (PLGA) (HA/PLGA and BO/PLGA) were evaluated concerning cytotoxicity, genotoxicity and mutagenicity as potential candidates for bone repair. The materials were developed and provided by Bionnovation Biomedical Products Ltda. Eluates from these bone substitutes were prepared for toxicity evaluations using eukaryotic cell cultures. HA/PLGA was used as a comparison for Bonefill®. Cell viability was evaluated by XTT assay and surviving fraction was calculated for clonogenic survival. Additionally, tail moment was used to assess genotoxicity (comet assay). The frequencies of binucleated cells with micronucleus (FBMN), micronucleus (FMN), nucleoplasmic bridges (NPBs), and nuclear buds (NBUDs) were analysed by cytokinesis-block micronucleus assay (CBMN assay). Results showed no statistical difference in cell viability compared with negative control (NC) The eluates did not promote delayed cytotoxicity whereas the surviving fraction rate for cultured cells was similar to NC. Furthermore, no genotoxicity or mutagenicity effects were observed for cultured cells with the Bonefill/PLGA and HA/PLGA eluates. In conclusion, the negative cytotoxicity, genotoxicity and mutagenicity results indicate that these bone substitutes presented interesting preliminary results as potential biomaterials for bone repair.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:37:53Z
2018-12-11T17:37:53Z
2018-01-01
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/10.1590/s2175-97902018000217438
Brazilian Journal of Pharmaceutical Sciences, v. 54, n. 2, 2018.
2175-9790
1984-8250
http://hdl.handle.net/11449/180070
10.1590/s2175-97902018000217438
S1984-82502018000200611
2-s2.0-85050856017
S1984-82502018000200611.pdf
url http://dx.doi.org/10.1590/s2175-97902018000217438
http://hdl.handle.net/11449/180070
identifier_str_mv Brazilian Journal of Pharmaceutical Sciences, v. 54, n. 2, 2018.
2175-9790
1984-8250
10.1590/s2175-97902018000217438
S1984-82502018000200611
2-s2.0-85050856017
S1984-82502018000200611.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences
0,214
0,214
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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 repositoriounesp@unesp.br
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