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pubmed-article:19361853pubmed:dateCreated2009-7-6lld:pubmed
pubmed-article:19361853pubmed:abstractTextComonomers used in dental restorative materials, e.g. triethylenglycoledimethacrylate (TEGDMA), hydroxyethylmethacrylate (HEMA) and methylmethacylic acid (MMA) are methacrylic acid esters. Because of the chemical structure of these esters in earlier studies two different in vitro pathways were suggested. The present study was performed in order to analyze which of these chemical pathways is preferred in vitro: (a) saponification of TEGDMA, HEMA, and MMA leading to free methacrylic acid (MA) as an ionic intermediate or (b) enzymatically epoxidation of mother compounds leading to lipophilic intermediates.lld:pubmed
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pubmed-article:19361853pubmed:year2009lld:pubmed
pubmed-article:19361853pubmed:articleTitleIn vitro stability of methylmethacrylic acid, TEGDMA and HEMA exposed to esterases.lld:pubmed
pubmed-article:19361853pubmed:affiliationWalther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University of Munich, 80336 Munich, Germany. mario.seiss@gmx.delld:pubmed
pubmed-article:19361853pubmed:publicationTypeJournal Articlelld:pubmed