Method: The nanogels were synthesized through solution copolymerization of either isodecyl methacrylate (IDMA) or isobornyl methacrylate (IBMA) with bisphenol-A-ethoxylate diacrylate (BisEA). They were added at 5, 10, or 25 wt% to a 70/30 mass ratio of ethoxylated bisphenol-A-dimethacrylate and triethylene glycol dimethacrylate (control). The nanogel Tg was characterized (dynamic mechanical analysis) along with evaluation of resin reaction kinetics/conversion (near-infrared spectroscopy), mechanical properties (three-point bending on a universal testing device) and polymerization stress (tensometer).
Result: The nanogel compositions provided Tg values of -46°C and -24°C for IDMA/BisEA and IBMA/BisEA, respectively. The table below shows conversion, stress, and mechanical properties for each material. Compared to the control, degree of conversion increased by as much as 20%. Modulus values increased by as much as 38% with 5wt% nanogel additives, but at the 25wt% level, mechanical properties dropped by up to 40%.
Material |
Conversion (%) |
Stress (MPa) |
Modulus (GPa) |
Flex. Strength (MPa) |
Control |
72.0±2.2 |
2.3±0.1 |
1.3±0.1 |
61.7±2.9 |
IDMA/BisEA 5% |
79.9±0.6 |
2.6±0.2 |
1.4±0.0 |
57.8±2.9 |
IDMA/ BisEA 10% |
81.2±0.8 |
2.5±0.1 |
1.3±0.1 |
55.7±3.0 |
IDMA/ BisEA 25% |
85.3±0.4 |
1.8±0.1 |
0.8±0.0 |
37.0±1.4 |
IBMA/ BisEA 5% |
77.0±0.7 |
2.7±0.0 |
1.8±0.1 |
73.4±3.1 |
IBMA/ BisEA 10% |
78.9±1.1 |
2.5±0.0 |
1.7±0.0 |
70.3±2.2 |
IBMA/ BisEA 25% |
82.6±1.6 |
1.9±0.1 |
1.6±0.0 |
62.2±0.5 |
Conclusion: Our results suggest that low Tg nanogels can be used at relatively low concentrations to improve local conversion and mechanical properties of dental resins, without substantially affecting stress development.
Keywords: Biomaterials, Polymerization and Polymers