The paper reviews the environmental factors affecting ageing processes, and the degradation of resins, filler, and the filler-matrix interface. It discusses the current methods of testing materials in vitro. A review of literature was conducted with the main sources being PubMed. ScienceDirect, Mendeley, and Google Scholar were used as other resources. Studies were selected based on relevance, with a preference given to recent research. The ageing process is an inherent element of the use of resin composites in the oral environment, which is very complex and changes dynamically. The hydrolysis of dental resins is accelerated by some substances (enzymes, acids). Bonds formed between coupling agent and inorganic filler are prone to hydrolysis. Methods for prediction of long-term behaviour are not included in composite standards. Given the very complex chemical composition of the oral environment, ageing tests based on water can only provide a limited view of the clinical performance of biomaterial. Systems that can reproduce dynamic changes in stress (thermal cycling, fatigue tests) are better able to mimic clinical conditions and could be extremely valuable in predicting dental composite clinical performance. It is essential to identify procedure to determine the ageing process of dental materials.

There are many methods widely applied in the engineering of biomaterials to improve the mechanical properties of the dental composites. The aim of this study was to assess the effect of modification of dental composites with liquid rubber on their mechanical properties, degree of conversion, viscosity, and cytotoxicity. Both flow and packable composite consisted of a mixture of Bis-GMA, TEGDMA, UDMA, and EBADMA resins reinforced with 60 and 78 wt.% ceramic filler, respectively. It was demonstrated that liquid rubber addition significantly increased the fracture toughness by 9% for flow type and 8% for condensable composite. The influence of liquid rubber on flexural strength was not statistically significant. The addition of the toughening agent significantly reduced Young’s modulus by 7% and 9%, respectively, while increasing deformation at breakage. Scanning electron microscopy (SEM) observations allowed to determine the mechanisms of toughening the composites reinforced with ceramic particles. These mechanisms included bridging the crack edges, blocking the crack tip by particles and dissipation of fracture energy by deflection of the cracks on larger particles. The degree of conversion increased after modification, mainly due to a decrease in the matrix resin viscosity. It was also shown that all dental materials were nontoxic according to ISO 10993-5, indicating that modified materials have great potential for commercialization and clinical applications.

This paper describes morphological differences and associated functional properties of dental composites based on dimethacrylate resins reinforced by nanoparticulate silica filler modified according to different silanization procedures. Surface morphology of the materials was evaluated by means of AFM, while nanohardness and elasticity modulus of the surface layer - by nanoindentation and abrasion - gravimetrically. The effects of silane treatment of nanoparticulate silica surface on possible filler loading, mechanical properties and abrasion resistance of the composites were discussed. The influence of the amount and kind of silane coupling agent on the example of 3 -methacryloxypropyltrimethoxysilane and vinyltrimethoxysilane were presented. The modification of nanoparticulate silica with 3 -methacryloxypropyltrimethoxysilane enabled the introduction of 15% more filler than modification with vinyltrimethoxysilane. The abrasion resistance depended strongly on the composite morphology and the micromechanical parameters of the surface layer. The composite modified with vinyltrimethoxysilane, containing the highest percentage of filler particles smaller than 1 μm in diameter, exhibited the lowest abrasion (0.3 vol.%). Abrasive wear seemed to be a linear function of nanoindentation hardness with the correlation coefficient of R2 = 0.96. The highest hardness of the surface layer of commercial composite (130 MPa) resulted in the highest abrasive wear (7.7 vol.%). The type and the quantity of silane coupling agent used for silica modification strongly influence the morphology and mechanical and tribological properties of the dental composites. The application of more than the calculated, optimal amount of silane to nanosilica modification enables higher filler loading, but the composites exhibit inferior mechanical characteristics. Nanoindentation hardness of surface layer showed to be the most useful parameter in estimation of material susceptibility to abrasion.

Aim of the study was to evaluate mechanical properties of light-curing composite materials modified with the addition of calcium fluoride. The study used one experimental light-curing composite material (ECM) and one commercially available flowable light-curing composite material (FA) that were modified with 0.5–5.0 wt% anhydrous calcium fluoride. Morphology of the samples and uniformity of CaF2 distribution were analyzed using Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). Mechanical properties were tested after 24-hour storage of specimens in dry or wet conditions. Stored dry ECM enriched with 0.5–1.0 wt% CaF2 showed higher tensile strength values, while water storage of all modified ECM specimens decreased their tensile strength. The highest Vickers hardness tested after dry storage was observed for 2.5 wt% CaF2 content in ECM. The addition of 2.0–5.0 wt% CaF2 to FA caused significant decrease in tensile strength after dry storage and overall tensile strength decrease of modified FA specimens after water storage. The content of 2.0 wt% CaF2 in FA resulted in the highest Vickers hardness tested after wet storage. Commercially available composite material (FA), unmodified with fluoride addition, demonstrated overall significantly higher mechanical properties.