The effect of placement of ultra-high molecular weight polyethylene (UHMWPE) fibres on the flexural properties and fracture resistance of a direct dental composite was investigated. The UHMWPE fibres are increasingly being used for the reinforcement of laboratory fabricated resin composite crown and bridgework. The aim of this study was to assess the effect of a commonly used laboratory fabrication variable on the in vitro strength of beam shaped specimen simulating a three-unit fixed bridge. Four groups (10 specimens per group) of Herculite XRV were prepared for flexural modulus and strength testing after reinforcement with UHMWPE fibres. Two groups of control specimens were prepared without any fibre reinforcement. Half the specimen groups were stored in distilled water and the other groups were stored dry, both at 37 degrees C for 2 weeks before testing. The results of this study showed that placement of fibre at or slightly away from the tensile side improved the flexural properties of the composite in comparison with the unreinforced control specimen groups whilst the mode of failure differed according to fibre position. Scanning electron microscope (SEM) investigation revealed that placement of the fibre slightly away from the tensile side favoured crack development and propagation within the resin bridging the interfibre spaces in addition to debonding parallel to the direction of fibre placement. Laboratory fabrication variables may effect the strength of fibre reinforced bridgework significantly.

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New BioRoot RCS was not toxic whilst Hybrid Root SEAL demonstrated more toxicity and DNA double-strand breaks when compared with other resin- and silicate-based root canal sealers.

Given the accumulated evidence on the effects of water-in-deep eutectic solvents (DESs) on the solvent nanostructure and the yield of lipase reactions, here we have used molecular dynamics (MD) simulations to delineate the structure and dynamics of thermoalkalophilic lipases in choline chloride/urea-based DES (reline) with varying hydration levels. Results indicated that pure reline almost froze the lipase backbone, while hydrated reline that showed a less ordered nanostructure than the pure form introduced some fluctuations to lipase structures, particularly to the lid domain. Although none of the solvents led to unfolding, solvation by 8 M urea or water when accompanied with elevated temperature caused the most significant loss of secondary structure. Experimental results indicated that lipase incubation in slightly hydrated reline [5% (v/v)] led to the highest level of residual activity, implying interfacial activation. Overall, we report that slightly hydrated reline activates thermoalkalophilic lipases, consistent with the particular MD observation showing enhanced mobility of the lid domain. These insights provided by this study contribute to designing efficient lipase applications in DES-based reaction media, giving cues for customizing water-in-DESs for optimal enzyme stability and activity.