Objective: To examine the effect additives have on MTA’s setting time and setting reaction using differential scanning calorimetry (DSC).
Method: ProRoot MTA (Dentsply Tulsa Dental) powder was prepared with distilled water, phosphate buffered saline (PBS), CaCl2, 3% NaOCl, or lidocaine in a 3:1 mixture and sealed in crucibles for DSC evaluation. The setting reaction exotherms were evaluated at 37°C for 8 hours to determine setting time. Separate samples were stored and evaluated by dynamic scan DSC (37-640°C @10°C/min) at 1 day, 1 week, and 1 month (n=9/group/time). Dynamic DSC quantifies reaction product formed from the amount of heat required to decompose it. Thermogram peaks were integrated to determine enthalpy which was analyzed with ANOVA/Tukey (a=.05).
Result: Isothermal DSC identified two main peaks occurring at 25-50 minutes and 4.5-6 hours for the control, while additive groups had earlier peaks indicating a decreased setting time. The dynamic DSC scans produced an endothermic peak around 450-600°C attributed to Ca(OH)2 decomposition. Enthalpy values were:
Group |
Ca(OH)2 Decomposition Enthalpy (J/g) |
||
1 Day |
1 Week |
1 Month |
|
Control |
70.1±17.5 C |
138.5±13.5 A |
98.8±8.6 A |
CaCl2 |
100.3±8.6 A |
117.4±6.9 B |
96.0±11.0 AB |
NaOCl |
24.1±8.0 D |
39.2±6.8 D |
22.9±8.3 D |
PBS |
93.9±16.1 AB |
116.8±12.4 B |
82.1±14.4 B |
Lidocaine |
74.1±29.7 BC |
87.2±6.6 C |
59.6±11.7 C |
Different letters denote significant (p˂0.05) differences. The use of a few additives (NaOCl/Lidocaine) resulted in significantly less Ca(OH)2 product formation.
Conclusion: Consideration of the chemistry of MTA hydration is needed when certain additives are contemplated when mixing MTA.
Keywords: Chemical, Dental materials and Endodontics