Author/Authors :
Tabari, Kasra Dental Research Center - Research Institute of Dental Sciences - Dental School, Shahid Beheshti University of Medical Sciences, Tehran , Hosseinpour, Sepanta Research Fellow - Dental Research Center - Research Institute of Dental Sciences - Students' Research Committee - Shahid Beheshti University of Medical Sciences, Tehran , Parashos, Peter Melbourne Dental School, University of Melbourne - Melbourne - Victoria, Australia , Kardouni Khozestani, Parisa Pathology Department - Dental School, Gilan University of Medical Sciences, Rasht , Rahimi, Hossein Mohammad Students' Research Committee - Dental School, Shahid Beheshti University of Medical Sciences, Tehran
Abstract :
Introduction: Nanoparticles are being increasingly applied in dentistry due to their
antimicrobial and mechanical properties. This in vitro study aimed to assess and compare the
cytotoxicity of four metal oxide nanoparticles (TiO2, SiO2, ZnO, and Al2O3) on human dental
pulp stem cells. Methods and Materials: Four suspension with different concentrations (25,
50, 75, 100 μg/mL) of each nanoparticle were prepared and placed into cavities of three 96-
well plates (containing 1×104 cells per well that were seeded 24 earlier). All specimens were
incubated in a humidified incubator with 5% CO2 at 37°C. Mosmann’s Tetrazolium Toxicity
(MTT) assay was used to determine in vitro cytotoxicity of test materials on pulpal stem cells.
Cell viability was determined at 24, 48, and 72 h after exposure. Data comparisons were
performed using a general linear model for repeated measures and Tukey's post hoc test. The
level of significance was set at 0.05. Results: The tested nanoparticles showed variable levels
of cytotoxicity and were dose and time dependant. The minimum cell viability was observed
in ZnO followed by TiO2, SiO2 and Al2O3. Conclusion: The results demonstrated that cell
viability and morphological modifications occurred at the concentration range of 25 to 100
μg/mL and in all nanoparticles. The higher concentration and longer duration of exposure
increased cellular death. Our results highlight the need for a more discrete use of
nanoparticles for biomedical applications.