Biological and physicochemical properties of carbon-graphite fibre-reinforced polymers intended for implant suprastructures

Segerström S, Sandborgh‐Englund G, Ruyter EI. Biological and physicochemical properties of carbon‐graphite fibre‐reinforced polymers intended for implant suprastructures. Eur J Oral Sci 2011; 119: 246–252. © 2011 Eur J Oral Sci The aim of this study was to determine water sorption, water solubility, dimensional change caused by water storage, residual monomers, and possible cytotoxic effects of heat‐polymerized carbon‐graphite fibre‐reinforced composites with different fibre loadings based on methyl methacrylate/poly(methyl methacrylate) (MMA/PMMA) and the copolymer poly (vinyl chloride‐co‐vinyl acetate). Two different resin systems were used. Resin A contained ethylene glycol dimethacrylate (EGDMA) and 1,4‐butanediol dimethacrylate (1,4‐BDMA); the cross‐linker in Resin B was diethylene glycol dimethacrylate (DEGDMA). The resin mixtures were reinforced with 24, 36 and 47 wt% surface‐treated carbon‐graphite fibres. In addition, polymer B was reinforced with 58 wt% fibres. Water sorption was equal to or below 3.34 ± 1.18 wt%, except for the 58 wt% fibre loading of polymer B (5.27 ± 1.22 wt%). Water solubility was below 0.36 ± 0.015 wt%, except for polymer B with 47 and 58 wt% fibres. For all composites, the volumetric increase was below 0.01 ± 0.005 vol%. Residual MMA monomer was equal to or below 0.68 ± 0.05 wt% for the fibre composites. The filter diffusion test and the (3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide) (MTT) assay demonstrated no cytotoxicity for the carbon‐graphite fibre‐reinforced composites, and residual cross‐linking agents and vinyl chloride were not detectable by high‐performance liquid chromatography (HPLC) analysis.