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Endodontic Materials in Clinical Practice


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[137, 138], giving it a shorter setting time of 10–15 minutes [139, 140]. As ProRoot MTA and MTA Angelus are based on Portland cement and thus manufactured from naturally occurring raw materials, it is conceivable that they contain traces of heavy metals such as arsenic, lead, and chromium [138, 141, 142]. In an attempt to prevent this contamination, other manufacturers use pure laboratory‐grade materials. The HCSCs Bioaggregate (Innovative Bioceramix Inc., Vancouver, Canada) and Biodentine (Septodont, Saint Maur des Fosses, France) have been manufactured using this approach. Bioaggregate is composed predominantly of tricalcium silicate, with additions of calcium phosphate, silicon dioxide, and tantalum oxide used as a radiopacifier. Biodentine powder predominantly consists of tricalcium silicate as the core material, along with dicalcium silicate, calcium carbonate (filler), iron oxide (shade), and zirconium oxide (radiopacifier) [143]. It differs from other HCSCs in that its liquid phase has active components, namely calcium chloride (accelerator) and a hydrosoluble polymer (water‐reducing agent) [144]. The manufacturer approximates its setting time at between 9 and 12 minutes [145]. It has been suggested that it is longer in reality, however.

      A workable mix of HCSC requires the addition of more water than is necessary for hydration. This results in a system of pores which reduces over time as the water is used up in hydration [146]. Generally, the total pore space is equivalent to the initial water‐to‐powder ratio; therefore, increasing the water‐to‐powder ratio increases the pore space [146, 147]. Ionic exchange between the cement surface and the fluid surrounding it leads to the liberation of a number of different leachable ions from the surface in an aqueous environment.

      In order for a material to be regarded as clinically successful as a pulp‐capping agent, it should demonstrate a number of important characteristics, as outlined earlier. Since their introduction, HCSCs have undergone extensive in vitro and in vivo analysis [148]. Their antimicrobial and antifungal effects show conflicting results, with an antibacterial effect found on some facultative bacteria, but no effect on any strict anaerobes; however, the same study showed that zinc oxide‐eugenol‐based materials tested in parallel led to inhibition of growth amongst both types of bacteria [149]. An assessment using single‐strain and polymicrobial broths of bacteria and fungi showed that MTA inhibited fungal and microbial growth in both [150]. Interestingly, grey MTA was shown to inhibit similar amounts of growth of Streptococcus sanguis to white MTA at lower concentrations, suggesting that it may have greater antibacterial activity [151]. Attempts have been made to enhance the antibacterial properties of HCSCs by combining them with chlorhexidine instead of water, at concentrations of 0.12% [152] and 2% [153] – both proved successful, but other authors have expressed doubts about their utility in terms of biocompatibility [154] and deterioration of physical characteristics [153]. Although in vitro microleakage studies are frequently viewed with scepticism [155–157], they are the main means of determining the ability of a material to create a barrier against bacterial penetration in a given clinical scenario. Numerous different in vitro techniques have been used to compare the sealing ability of HCSCs to other materials used in the same clinical situation, with HCSCs showing superior to amalgam, super EBA (ethoxy benzoic acid), and intermediate restorative material (IRM) with techniques including dye leakage [158, 159], fluid filtration [160, 161], and bacterial penetration studies [149, 162, 163].

Schematic illustration of (a) Diagrammatic representation of dentine, including inorganic and organic components, at a nanometre scale. (b) Immersion of dentine in tissue fluid or extracellular exudate that has interacted locally with calcium silicate cement and has a unique ionic composition. (c) Ionic exchange between dentine and soluble components of calcium silicate cements, resulting in disruption of hydroxyapatite crystals, leading to solubilization and release of bioactive molecules from dECM, including noncollagenous proteins, glycosaminoglycans, and growth factors.

      Several in vitro studies have been carried out comparing TheraCal to other VPT agents. It has been demonstrated to be cytotoxic with pulp cells [186, 187], and it shows more significant inflammation and less bioactive potential than Biodentine [187]. The authors of the latter study even suggested it should not be considered a candidate for direct interfacing with the pulp.

      TheraCal does not perform as well as conventional water‐based HCSCs when interfacing with the pulp itself [188]. In a study