Dental Research Today is a free monthly online journal that collates and summarizes the latest research about Dental, including details on implants, health, hygiene, cosmetic, dentistry. | ||||||||
|
Effects of molecular structure of the resins on the volumetric shrinkage and the mechanical strength of dental restorative composites.Kim LU, Kim JW, Kim CK School of Chemical Engineering and Materials Science, Chung-Ang University, 221 Huksuk-dong. Dongjak-gu, Seoul 156-756, Korea. To prepare a dental composite that has a low amount of curing shrinkage and excellent mechanical strength, various 2,2-bis[4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane (Bis-GMA) derivatives were synthesized via molecular structure design, and afterward, properties of their mixtures were explored. Bis-GMA derivatives, which were obtained by substituting methyl groups for hydrogen on the phenyl ring in the Bis-GMA, exhibited lower curing shrinkage than Bis-GMA, whereas their viscosities were higher than that of Bis-GMA. Other Bis-GMA derivatives, which contained a glycidyl methacrylate as a molecular end group exhibited reduced curing shrinkage and viscosity. Methoxy substitution for hydroxyl groups on the Bis-GMA derivatives was performed for the further reduction of the viscosity and curing shrinkage. Various resin mixtures, which had the same viscosity as the commercial one, were prepared, and their curing shrinkage was examined. A resin mixture containing 2,2-bis[3,5-dimethyl, 4-(2-methoxy-3-methacryloyloxy propoxy) phenyl] propane] (TMBis-M-GMA) as a base resin and 4-tert-butylphenoxy-2-methyoxypropyl methacrylate (t-BP-M-GMA) as a diluent exhibited the lowest curing shrinkage among them. The composite prepared from this resin mixture also exhibited the lowest curing shrinkage along with enhanced mechanical properties. Published 11 September 2006 in Biomacromolecules, 7(9): 2680-7.
© 2004-2008 Dental Research Today. All Rights Reserved. |
| ||||||