Cytotoxicity and genotoxicity of calcium silicate-based cements on an osteoblast lineage

Ana Lívia Gomes-Cornélio1, Elisandra Márcia Rodrigues1, Leticia Boldrin Mestieri1

  • 1Universidade Estadual Paulista - UNESP, Araraquara School of Dentistry, Department of Restorative Dentistry, Araraquara, SP, Brazil.

Insights

This study assessed the biocompatibility of calcium silicate cements (CSC) and their modified forms in human osteoblast cells. CSC and CSCR2 showed promising results, indicating potential as reparative biomaterials with low cytotoxicity and genotoxicity.

Area of Science:

  • Biomaterials Science
  • Dental Materials
  • Cell Biology

Background:

  • Calcium silicate-based biomaterials, including Mineral Trioxide Aggregate (MTA), are increasingly developed.
  • Evaluating the biocompatibility of novel calcium silicate cements (CSC) and their modified formulations is crucial for clinical application.

Purpose of the Study:

  • To assess the cytotoxicity, genotoxicity, and apoptosis/necrosis of pure CSC, modified CSC (CSCM), and resin-based CSCR cements.
  • To compare the biological responses of human osteoblast cells (SAOS-2) exposed to these cements.

Main Methods:

  • Human osteoblast cells (SAOS-2) were exposed to cement extracts for 24 hours.
  • Cytotoxicity was evaluated using the methyl-thiazolyl tetrazolium (MTT) assay.
  • Genotoxicity was assessed via the comet assay, and apoptosis/necrosis was measured using a specific assay.

Main Results:

  • No significant differences in cell viability were observed among most materials at 2 mg/mL and 10 mg/mL concentrations via MTT assay.
  • CSCR3 showed reduced cell viability at 10 mg/mL, and CSC at 50 mg/mL.
  • CSCR1, CSCR2, and CSCR3 exhibited higher initial apoptosis rates compared to controls.
  • Comet assay revealed no genotoxicity for any cement at 2 mg/mL; CSC and CSCR2 were also non-genotoxic at 10 mg/mL.

Conclusions:

  • All tested experimental materials demonstrated cell viability.
  • Calcium silicate cements (CSC) and CSCR2 showed favorable responses in apoptosis and genotoxicity assessments at 10 mg/mL.
  • These findings suggest considerable potential for CSC and CSCR2 as reparative biomaterials.

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