Both Biodentine and MTA caused the uptake of Ca and Si in the adjacent root canal dentine in the presence of PBS. The dentine element uptake was more prominent for Biodentine than MTA.
Compared with Biodentine and WMTA, BC sealer showed less Ca ion release and did not show Ca and Si incorporation as deeply in human root canal dentine when immersed in PBS for up to 90 days.
Defense reactions of the dentin/pulp complex involve a variety of biological systems, in which the immune system plays a pivotal role. The knowledge of the organization and function of pulpal immunocompetent cells has been sparse, but in recent years a significant body of information of immune mechanisms in general has provided a footing for substantial new knowledge of the immune mechanisms of the dental pulp. The identification of pulpal dendritic cells (DCs) has generated research activities which have led to a concept of how an antigenic challenge may evoke a pulpal inflammatory response. Although DCs are not able to identify foreign antigens specifically, they provide necessary signals to activate T-lymphocytes which in turn will orchestrate other immunocompetent cells to mount the local immune defense of the dental pulp. The purpose of this review is to accent the organization and function of pulpal DCs and other tissue and cellular components and to provide a basis for how they may interact to instigate pulpal defense mechanisms.
This paper aims to
review the biological and physicochemical
properties of mineral trioxide aggregate (MTA)
with respect to its ability to induce reparative
dentinogenesis, which involves complex cellular
and molecular events leading to hard-tissue
repair by newly differentiated odontoblast-like
cells. Compared with that of calcium
hydroxide-based materials, MTA is more efficient
at inducing reparative dentinogenesis in vivo.
The available literature suggests that the
action of MTA is attributable to the natural
wound healing process of exposed pulps, although
MTA can stimulate hard-tissue-forming cells to
induce matrix formation and mineralization in
vitro. Physicochemical analyses have revealed
that MTA not only acts as a “calcium
hydroxide-releasing” material, but also
interacts with phosphate-containing fluids to
form apatite precipitates. MTA also shows better
sealing ability and structural stability, but
less potent antimicrobial activity compared with
that of calcium hydroxide. The clinical outcome
of direct pulp capping and pulpotomy with MTA
appears quite favorable, although the number of
controled prospective studies is still limited.
Attempts are being conducted to improve the
properties of MTA by the addition of setting
accelerators and the development of new calcium
silicate-based materials.
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