Dental Materials
Volume 25, Issue 4 , Pages 481-485, April 2009

Excretion of dental resin monomers and metabolic intermediates via urine in guinea pigs

  • Mario Seiss

      Affiliations

    • Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University of Munich, 80336 Munich, Germany
    • Department of Operative Dentistry and Periodontology, Ludwig-Maximilians-University, 80336 Munich, Germany
    • Corresponding Author InformationCorresponding author at: Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University of Munich, Goethestr. 31, D-80336 Munich, Germany. Tel.: +49 89 2180 73806.
  • ,
  • Wolfgang Marquardt

      Affiliations

    • Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University of Munich, 80336 Munich, Germany
  • ,
  • Reinhard Hickel

      Affiliations

    • Department of Operative Dentistry and Periodontology, Ludwig-Maximilians-University, 80336 Munich, Germany
  • ,
  • Franz-Xaver Reichl

      Affiliations

    • Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University of Munich, 80336 Munich, Germany
    • Department of Operative Dentistry and Periodontology, Ludwig-Maximilians-University, 80336 Munich, Germany

Received 12 June 2007; received in revised form 22 July 2008; accepted 13 August 2008.

Abstract 

Objective

Monomers like BisGMA (Bisphenol-A-glycidyldimethacrylate) and comonomers like TEGDMA (triethyleneglycoldimethacrylate) are used in dental restorative materials in order to build up the three-dimensional network of filling materials. Since earlier investigations revealed uptake and subsequent metabolism of unpolymerized remainders of (co)monomers, the present experiment investigates the metabolic urine pattern of guinea pigs (n=4) after application of TEGDMA or BisGMA (each dose=0.02mmol/kg body weight=100%), respectively.

Methods

For the investigations BisGMA was pre-dissolved in DMSO and subsequently diluted with 0.9% NaCl solution (final DMSO concentration 1%) and TEGDMA was dissolved in 0.9% NaCl solution. The solutions were administered with a gastric tube into the animals. Control animals received either 0.9% NaCl or 0.9% NaCl solution with 1% DMSO solution.

Results

After 24h in collected urine the following metabolites were identified. After administration of TEGDMA (mean relative concentration of administered substances)±s.d. [%]; n=4): unchanged TEGDMA: 12±1.5%, MA: 2.4±0.8%, and triethyleneglycol: 35±2.2%. After administration of BisGMA (mean±s.d. [%]; n=4): unchanged BisGMA: 11.4±2.7%, MA: 2.2±0.6%, and bisphenol-A-bis(2,3-dihydroxypropyl)ether: 60.1±5.2%).

Conclusion

No further metabolites like the previously identified intermediate 2,3-epoxymethacrylic acid and derived reaction products were identified in the urine, indicating that these metabolites must have reacted further.

Keywords: TEGDMA, BisGMA, Metabolites, Urine

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PII: S0109-5641(08)00250-9

doi:10.1016/j.dental.2008.08.013

Dental Materials
Volume 25, Issue 4 , Pages 481-485, April 2009