Author/Authors :
Moshary, AA Department of Endodontics - Member Ship of Dental Material Research Center - Faculty of Dentistry - Tehran Medical Sciences - Islamic Azad University - Tehran, Iran , Almasi, M No affiliation , Bitaraf, T Dental Implant Research Center - Dental Faculty - Tehran Medical Sciences - Islamic Azad University - Tehran, Iran
Abstract :
The aim of this study was to compare the cytotoxicity
of ProRoot MTA and Endocem at different times and concentrations on human
gingival fibroblasts.
Materials and Methods: In this in-vitro study, ProRoot MTA and Endocem extracts
with concentrations of 3, 6, 12, 25, and 50 mg/ml in the unhardened state
(solution) at 24, 48, and 72 hours on human gingival fibroblasts were transferred
to 96-well plates in Dulbecco’s Modified Eagle’s medium (DMEM). For each
material at any time and any concentration, three wells were used, and 90 samples
were examined. Also, to calibrate the cytotoxicity measuring device at 24, 48, and
72 hours, 3 wells for positive control and 3 wells for negative control have been
considered, which include a total of 9 positive control wells and 9 negative control
wells. Samples were analyzed by MTT assay. Data were analyzed by analysis of
variance (ANOVA).
Result: In the present study, the samples in the two groups at different times
and concentrations did not show a significant difference in terms of cytotoxicity
(P<0.05). The highest cytotoxicity was related to Endocem at 24 hours and a concentration
of 50 mg/ml, and the lowest was related to ProRoot MTA at 72 hours
and a concentration of 6 mg/ml.
Conclusion: According to the research, in general, the degree of cytotoxicity of
Endocem is comparable to that of ProRoot MTA.
Keywords :
MTT Assay , ProRoot MTA , Endocem , Cytotoxicity