AIM To evaluate the long-term sealing ability of four contemporary endodontic sealers [Pulp Canal Sealer (PCS), AH-Plus, GuttaFlow and Epiphany] using a fluid filtration technique. METHODOLOGY The palatal roots of 40 human maxillary molar teeth were selected and the root canal was prepared using a crown-down technique (apical size 40, 6% taper). Roots were irrigated with 3% NaOCl, 17% EDTA solution and rinsed with distilled water. Canals were filled with either PCS, AH-Plus, GuttaFlow or Epiphany using a single-cone technique (n = 8). Twenty-four hours after filling, the roots were connected to an automatic flow-recording device (Flodec System) filled with double-distilled water under pressure (0.2 bar) to measure leakage. Flow rates were assessed at 6, 12 or 24-h and after 1-year of storage. RESULTS None of the materials fully prevented fluid flow. Fluid flow decreased after 6 h and decreased further after 12 h. After 24 h, PCS and AH-Plus allowed significantly more fluid flow than GuttaFlow and Epiphany. After 1 year, PCS allowed significantly more fluid flow than the other materials. No significant changes in leakage occurred between 24 h and 1 year. CONCLUSIONS GuttaFlow and Epiphany allowed less fluid movement along filled straight roots.
Highly filled composites, Ormocers (organically modified ceramics) and 'smart' materials have been developed to overcome the polymerization shrinkage problems of conventional composite materials. The purpose of the current study was to investigate the effect of longer-term (up to 8 weeks) ageing of these resin-based dental restorative materials and determine the effect of post-curing on cytotoxicity. Twelve discs of each material (Colombus/IDR, Definite/Degussa, Ariston pHc/Vivadent) were either light-cured (Lc) or light-cured and post-cured (Pc). For cytotoxicity testing, the discs were placed in contact with cell culture medium (DMEM) and incubated at 37 degrees C. Extracts from composite materials were collected after 24 h and weekly over a time period of 8 weeks. Cytotoxicity of the eluates to cultured fibroblasts (Balb/c3T3) were measured by the succinic dehydrogenase (SDH) activity (MTT assay) and the results expressed in percentage of negative controls (Teflon discs). The results showed that ageing significantly influenced the cytotoxicity of the materials. Except for Ariston pHc, materials were less cytotoxic after 8 weeks of ageing than they were in early intervals and post-curing was not generally useful in reducing cytotoxicity. The Ariston pHc was initially moderately toxic, but then become highly cytotoxic for 5 weeks before returning to initial levels. The current study demonstrated the importance of assessing the cytotoxicity of resin composite materials at multiple times.