Diffusion and concurrent solubility of self-adhering and new resin–matrix composites during water sorption/desorption cycles

Objectives estigate the kinetic process of water diffusion and mass change in new resin–matrix composites during water sorption/desorption cycles. s ew resin–matrix composites were investigated [Filtek® Silorane (FS), GC Gradia Direct Anterior (GDA), GC Gradia Direct Posterior (GDP), GC Kalore (GCK), Vertise® Flow (VF)]. Five disk-shaped specimens, per material (15.0 ± 0.1) mm diameter by (2.0 ± 0.1) mm, were prepared according to ISO 4049. Each disk was immersed separately in de-ionized water for 150 d and then reconditioned for 75 d; all at (37 ± 1) °C. Mass was measured at different time intervals. Perspex disks were used as control. Data analysis was done by repeated measures ANOVA, one-way ANOVA and Tukeyʹs post hoc test (p < 0.05). s ter sorption (μg/mm3) after 150 d immersion ranged from 13.51 μg/mm3 (±0.40) for FS to 71.96 μg/mm3 (±0.90) for VF. The solubility ranged up to 16.95 μg/mm3 (±0.79) for VF. A significant mass reduction occurred in VF after the peak value [73.63 μg/mm3 (±0.31)] of water sorption was reached at 42 d. VF had the highest diffusion-coefficient for sorption: 5.23 × 10−9 cm2/s (±0.38) and desorption: 11.72 × 10−9 cm2/s (±0.16). Percentage sorption differences were significant for all materials (p < 0.001), except between GCK and GDP. The early correlation between mass change and square root of time was linear. icance esin–matrix composite varied in sorption/desorption cycles which may affect clinical service. A concurrent solubility process occurred during sorption of the self-adhering composite VF. The silorane composite FS exhibited minimal sorption.