Table 3.
Study | Assay | Materials evaluated | Result |
---|---|---|---|
Hirschman et al. (2012)33 | TA: MTT-based colorimetric assay | White mineral trioxide aggregate cement (AMTA, MTA-Angelus), | AMTA, ERRM, and UBP had statistically similar cytotoxicity levels. However, Dycal demonstrated a statistically |
CL: Human dermal fibroblasts | Brasseler ERRM putty, Dycal, and Ultra-blend Plus (UBP) | significant cytotoxic effect | |
Type of contact (TC): Indirect | |||
Ma et al. (2011)37 | TA: MTT assay | ERRM Putty and Paste with gray MTA | (ERRM Putty) and Paste (ERRM Paste) showed similar in vitro biocompatibility as that of gray MTA |
CL: Gingival fibroblast | |||
Yoshino et al. (2013)34 | TA: MTT assay CL: Periodontal ligament |
White MTA, MTA Fillapex® and Portland cement (PC) | MTA Fillapex demonstrated the highest cytotoxic effect on periodontal ligament fibroblasts followed by white |
fibroblasts | MTA and PC | ||
TC: Indirect | |||
Zhou et al. (2015)35 | TA: Flow cytometry and electron microscopy | EndoSequence BC, MTA Fillapex, and AH Plus (control sealer) | The 2 calcium silicate-containing endodontic sealers demonstrated different cytotoxicities. MTA Fillapex of ≥2 |
CL: Human gingival fibroblasts | weeks demonstrated more toxicity than fresh/1-week-old cement. MTA Fillapex did not show toxicity at | ||
TC: Indirect | concentration ≥ 1:32. AH plus was not toxic after setting | ||
Mukhtar- | TA: MTT assay | BioAggregate and iRoot SP | Both the materials had acceptable biocompatibility and |
Fayyad (2011)38 | CL: Human fibroblast MRC-5 cells | their cytotoxic effects were concentration-dependent | |
TC: Indirect | |||
Zhou et al. (2013)36 | TA: Flow cytometry and electron microscopy | Biodentine, White ProRoot MTA, and glass ionomer cement | No significant difference in cell viability was noted between Biodentine and MTA, and they had a less |
CL: Human gingival fibroblasts | cytotoxic effect than glass ionomer cement | ||
TC: Indirect |