Comparison of cell viabilityand cytotoxicity of MTA,45S5 and niobiophosphatebioactive glass

Aim: This current in vitro study investigated the cytotoxicity and the ability to maintain cell viability of two bioglasses, the commercial 45S5 (Sylc®, OSspray Ltd, London, UK) and the experimental NbG (niobiophosphate bioactive glass), in comparison to MTA (MTA Angelus®, Parana, Brazil). Methods: In the cell viability assay, human gingival fibroblasts were exposed to the bioactive materials/cements (NbG; 45S5; and MTA) diluted in the cell culture medium. According to ISO 10993-5, a cytotoxic effect was considered when there was a decrease in cell viability of more than 30%. The three bioactive materials were also analyzed under SEM (TM 3030, Hitachi, Tokyo, Japan) to assess the mean particle size, and under EDX analysis (EDX-720, Shimadzu, Tokyo, Japan) to verify composition and the presence of contaminants. Results: Human gingival fibroblasts had the highest cell viability when exposed to NbG (p<0.001). The control group and the MTA group had similar values (p=0.2341). The lowest cell viability occurred for the 45S5 group (p<0.001). The average particle size of the materials tested was 5.2μm for 45S5; 54.0μm for NbG; and 4.0μm for MTA. 45S5 and NbG showed the presence of Si, Ca, and P. Conclusion: The 45S5 bioglass was cytotoxic to fibroblasts, while MTA was not. The addition of niobium into the bioglass composition is advantageous.

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Publication Details

Journal
Brazilian journal of oral sciences/Brazilian Journal of Oral Sciences
Published
2025-08-26
DOI
https://doi.org/10.20396/bjos.v24i00.8676454
Primary Topic
Bone Tissue Engineering Materials
Type
article
Field-Weighted Citation Impact
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article

Comparison of cell viabilityand cytotoxicity of MTA,45S5 and niobiophosphatebioactive glass

Marcos Eric Barbosa Brito, Amanda Palmeira Arruda Nogueira, Patrícia Maria Wiziack Zago, Ceci Nunes Carvalho et al.
Brazilian journal of oral sciences/Brazilian Journal of Oral Sciences
Bone Tissue Engineering Materials
article

Comparison of cell viabilityand cytotoxicity of MTA,45S5 and niobiophosphatebioactive glass

Marcos Eric Barbosa Brito, Amanda Palmeira Arruda Nogueira, Patrícia Maria Wiziack Zago, Ceci Nunes Carvalho, Renata Grazziotin‐Soares, José Roberto de Oliveira Bauer, Meire Coelho Ferreira, Bruna Laís Lins Gonçalves, Cyrene Piazera Silva Costa
article en

Abstract

Aim: This current in vitro study investigated the cytotoxicity and the ability to maintain cell viability of two bioglasses, the commercial 45S5 (Sylc®, OSspray Ltd, London, UK) and the experimental NbG (niobiophosphate bioactive glass), in comparison to MTA (MTA Angelus®, Parana, Brazil). Methods: In the cell viability assay, human gingival fibroblasts were exposed to the bioactive materials/cements (NbG; 45S5; and MTA) diluted in the cell culture medium. According to ISO 10993-5, a cytotoxic effect was considered when there was a decrease in cell viability of more than 30%. The three bioactive materials were also analyzed under SEM (TM 3030, Hitachi, Tokyo, Japan) to assess the mean particle size, and under EDX analysis (EDX-720, Shimadzu, Tokyo, Japan) to verify composition and the presence of contaminants. Results: Human gingival fibroblasts had the highest cell viability when exposed to NbG (p<0.001). The control group and the MTA group had similar values (p=0.2341). The lowest cell viability occurred for the 45S5 group (p<0.001). The average particle size of the materials tested was 5.2μm for 45S5; 54.0μm for NbG; and 4.0μm for MTA. 45S5 and NbG showed the presence of Si, Ca, and P. Conclusion: The 45S5 bioglass was cytotoxic to fibroblasts, while MTA was not. The addition of niobium into the bioglass composition is advantageous.

Brazilian journal of oral sciences/Brazilian Journal of Oral SciencesVol. 24
University of British Columbia (CA), Universidade Ceuma (BR), Faculdade São Leopoldo Mandic (BR), Universidade Federal do Maranhão (BR)
Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Maranhão
Openalex Percentile: Top 79%
Bone Tissue Engineering Materials
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