Literature DB >> 15705427

Properties of eight methacrylated beta-cyclodextrin composite formulations.

Latiff A Hussain1, Sabine H Dickens, Rafael L Bowen.   

Abstract

OBJECTIVES: Methacrylated beta-cyclodextrins (MCDs) are novel candidate dental monomers if all or some of the hydroxyl groups of beta-cyclodextrin are substituted with methacrylate groups. The main objective of this study was to evaluate mechanical properties of a number of composite formulations having MCDs as novel dental comonomers. The properties determined were flexural strength (FS), volumetric shrinkage (VS), and degree of conversion (DC).
METHODS: A mass fraction of 50% of MCD monomers was mixed with a mass fraction of 50% each of a series of dimethacrylate or monomethacrylate diluent comonomers to produce consistent formulations of a workable viscosity. For comparison a resin mixture of a mass fraction of 50% Bis-GMA and a mass fraction of 50% triethyleneglycol dimethacrylate (a typical dental resin mixture) was also studied. The mixtures were activated with camphorquinone and ethyl 4-dimethylamino benzoate. One part by mass of each activated resin formulation was mixed with three parts by mass of glass filler. Samples for the FS tests were prepared in (2 x 2 x 25) mm3 molds by light-curing the composites for 2 min on each side. The cured samples were immersed in 37 degrees C water for 24 h, and FS was measured with an Instron machine at a crosshead speed of 0.5 mm/min. VS was measured by a computer-controlled mercury dilatometer. DC was measured by near-infrared spectroscopy.
RESULTS: The properties of the MCD-based composites depended on the kind of diluent used. With these MCD monomers, diluents of triethyleneglycol dimethacrylate, 1,10-decamethylenediol dimethacrylate, or benzyl methacrylate yielded the best composite properties. SIGNIFICANCE: Although not yet fully optimized, MCD-based composite formulations containing triethyleneglycol dimethacrylate, 1,10-decamethylenediol dimethacrylate, or benzyl methacrylate yielded flexural strength and volumetric shrinkage values were comparable to those of the Bis-GMA/triethyleneglycol dimethacrylate controls. These findings lend support for further development and evaluations of polymerizable cyclodextrin derivatives for use in dental materials.

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Year:  2005        PMID: 15705427     DOI: 10.1016/j.dental.2004.03.007

Source DB:  PubMed          Journal:  Dent Mater        ISSN: 0109-5641            Impact factor:   5.304


  3 in total

Review 1.  Recent advances and developments in composite dental restorative materials.

Authors:  N B Cramer; J W Stansbury; C N Bowman
Journal:  J Dent Res       Date:  2010-10-05       Impact factor: 6.116

2.  New cyclodextrin hydrogels cross-linked with diglycidylethers with a high drug loading and controlled release ability.

Authors:  Carmen Rodriguez-Tenreiro; Carmen Alvarez-Lorenzo; Ana Rodriguez-Perez; Angel Concheiro; Juan J Torres-Labandeira
Journal:  Pharm Res       Date:  2006-12-07       Impact factor: 4.200

3.  Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations.

Authors:  Rafael L Bowen; Clifton M Carey; Kathleen M Flynn; Charles M Guttman
Journal:  J Res Natl Inst Stand Technol       Date:  2009-02-01
  3 in total

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