Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles

Detalhes bibliográficos
Autor(a) principal: Başak,Toğar
Data de Publicação: 2022
Outros Autores: Hasan,Türkez, Feray,Bakan, Enes,Arslan Mehmet, Abdulgani,Tatar, Ivana,Caccıatore, Ahmet,Hacımüftüoğlu, Kenan,Çadırcı, Di,Stefano Antonio, Adil,Mardinoğlu
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Archives of Biology and Technology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100302
Resumo: Abstract Nanoscale biomaterials are commonly used in a wide range of biomedical applications such as bone graft substitutes, gene delivery systems, and biologically active agents. On the other hand, the cytotoxic potential of these particles hasn’t yet been studied comprehensively to understand whether or not they exert any negative impact on the cellular structures. Here, we undertook the synthesis of beta-tricalcium phosphate (ß-TCP) and biphasic tricalcium phosphate (BCP) nanoparticles (NPs) and determine their concentration-dependent toxic effects in human fetal osteoblastic (hFOB 1.19) cell line. Firstly, BCP and β-TCP were synthesized using a water-based precipitation technique and characterized by X-Ray Diffraction (XRD), Raman Spectroscopy, and Transmission Electron Microscopy (TEM). The cytological effects of β-TCP and BCP at different concentrations (0-640 ppm) were evaluated by using 3- (4,5-dimethylthiazol-2-yl) -2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The total oxidative status (TOS) parameter was used for investigating oxidative stress potentials of the NPs. In addition, the study assessed the DNA damage product 8-hydroxy-2′-deoxyguanosine (8-Oxo-dG) level in hFOB 1.19 cell cultures. The results indicated that the β-TCP (above 320 ppm) and BCP (above 80 ppm) NPs exhibited cytotoxicity effects on high concentrations. It was also observed that the oxidative stress increased relatively as the concentrations of NPs increased, aligning with the cytotoxicity results. However, the NPs concentrations of 160 ppm and above increased the level of 8-OH-dG. Consequently, there is a need for more systematic in vivo and in vitro approaches to the toxic effects of both nanoparticles.
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spelling Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticlesβ-Tricalcium phosphatebiphasic calcium phosphatenanoparticlecytotoxicitytotal oxidative statusgenotoxicityAbstract Nanoscale biomaterials are commonly used in a wide range of biomedical applications such as bone graft substitutes, gene delivery systems, and biologically active agents. On the other hand, the cytotoxic potential of these particles hasn’t yet been studied comprehensively to understand whether or not they exert any negative impact on the cellular structures. Here, we undertook the synthesis of beta-tricalcium phosphate (ß-TCP) and biphasic tricalcium phosphate (BCP) nanoparticles (NPs) and determine their concentration-dependent toxic effects in human fetal osteoblastic (hFOB 1.19) cell line. Firstly, BCP and β-TCP were synthesized using a water-based precipitation technique and characterized by X-Ray Diffraction (XRD), Raman Spectroscopy, and Transmission Electron Microscopy (TEM). The cytological effects of β-TCP and BCP at different concentrations (0-640 ppm) were evaluated by using 3- (4,5-dimethylthiazol-2-yl) -2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The total oxidative status (TOS) parameter was used for investigating oxidative stress potentials of the NPs. In addition, the study assessed the DNA damage product 8-hydroxy-2′-deoxyguanosine (8-Oxo-dG) level in hFOB 1.19 cell cultures. The results indicated that the β-TCP (above 320 ppm) and BCP (above 80 ppm) NPs exhibited cytotoxicity effects on high concentrations. It was also observed that the oxidative stress increased relatively as the concentrations of NPs increased, aligning with the cytotoxicity results. However, the NPs concentrations of 160 ppm and above increased the level of 8-OH-dG. Consequently, there is a need for more systematic in vivo and in vitro approaches to the toxic effects of both nanoparticles.Instituto de Tecnologia do Paraná - Tecpar2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100302Brazilian Archives of Biology and Technology v.65 2022reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/1678-4324-2022200784info:eu-repo/semantics/openAccessBaşak,ToğarHasan,TürkezFeray,BakanEnes,Arslan MehmetAbdulgani,TatarIvana,CaccıatoreAhmet,HacımüftüoğluKenan,ÇadırcıDi,Stefano AntonioAdil,Mardinoğlueng2022-03-04T00:00:00Zoai:scielo:S1516-89132022000100302Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2022-03-04T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false
dc.title.none.fl_str_mv Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
title Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
spellingShingle Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
Başak,Toğar
β-Tricalcium phosphate
biphasic calcium phosphate
nanoparticle
cytotoxicity
total oxidative status
genotoxicity
title_short Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
title_full Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
title_fullStr Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
title_full_unstemmed Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
title_sort Synthesis and in Vitro Toxicity Assessment of Different Nano-Calcium Phosphate Nanoparticles
author Başak,Toğar
author_facet Başak,Toğar
Hasan,Türkez
Feray,Bakan
Enes,Arslan Mehmet
Abdulgani,Tatar
Ivana,Caccıatore
Ahmet,Hacımüftüoğlu
Kenan,Çadırcı
Di,Stefano Antonio
Adil,Mardinoğlu
author_role author
author2 Hasan,Türkez
Feray,Bakan
Enes,Arslan Mehmet
Abdulgani,Tatar
Ivana,Caccıatore
Ahmet,Hacımüftüoğlu
Kenan,Çadırcı
Di,Stefano Antonio
Adil,Mardinoğlu
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Başak,Toğar
Hasan,Türkez
Feray,Bakan
Enes,Arslan Mehmet
Abdulgani,Tatar
Ivana,Caccıatore
Ahmet,Hacımüftüoğlu
Kenan,Çadırcı
Di,Stefano Antonio
Adil,Mardinoğlu
dc.subject.por.fl_str_mv β-Tricalcium phosphate
biphasic calcium phosphate
nanoparticle
cytotoxicity
total oxidative status
genotoxicity
topic β-Tricalcium phosphate
biphasic calcium phosphate
nanoparticle
cytotoxicity
total oxidative status
genotoxicity
description Abstract Nanoscale biomaterials are commonly used in a wide range of biomedical applications such as bone graft substitutes, gene delivery systems, and biologically active agents. On the other hand, the cytotoxic potential of these particles hasn’t yet been studied comprehensively to understand whether or not they exert any negative impact on the cellular structures. Here, we undertook the synthesis of beta-tricalcium phosphate (ß-TCP) and biphasic tricalcium phosphate (BCP) nanoparticles (NPs) and determine their concentration-dependent toxic effects in human fetal osteoblastic (hFOB 1.19) cell line. Firstly, BCP and β-TCP were synthesized using a water-based precipitation technique and characterized by X-Ray Diffraction (XRD), Raman Spectroscopy, and Transmission Electron Microscopy (TEM). The cytological effects of β-TCP and BCP at different concentrations (0-640 ppm) were evaluated by using 3- (4,5-dimethylthiazol-2-yl) -2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The total oxidative status (TOS) parameter was used for investigating oxidative stress potentials of the NPs. In addition, the study assessed the DNA damage product 8-hydroxy-2′-deoxyguanosine (8-Oxo-dG) level in hFOB 1.19 cell cultures. The results indicated that the β-TCP (above 320 ppm) and BCP (above 80 ppm) NPs exhibited cytotoxicity effects on high concentrations. It was also observed that the oxidative stress increased relatively as the concentrations of NPs increased, aligning with the cytotoxicity results. However, the NPs concentrations of 160 ppm and above increased the level of 8-OH-dG. Consequently, there is a need for more systematic in vivo and in vitro approaches to the toxic effects of both nanoparticles.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100302
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100302
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4324-2022200784
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
dc.source.none.fl_str_mv Brazilian Archives of Biology and Technology v.65 2022
reponame:Brazilian Archives of Biology and Technology
instname:Instituto de Tecnologia do Paraná (Tecpar)
instacron:TECPAR
instname_str Instituto de Tecnologia do Paraná (Tecpar)
instacron_str TECPAR
institution TECPAR
reponame_str Brazilian Archives of Biology and Technology
collection Brazilian Archives of Biology and Technology
repository.name.fl_str_mv Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)
repository.mail.fl_str_mv babt@tecpar.br||babt@tecpar.br
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