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Preparation of a Bis-GMA-Free Dental Resin System with Synthesized Fluorinated Dimethacrylate Monomers

机译:含氟化二甲基丙烯酸酯单体的无Bis-GMA牙科树脂体系的制备

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With the aim of reducing human exposure to Bisphenol A (BPA) derivatives in dentistry, a fluorinated dimethacrylate monomer was synthesized to replace 2,2-bis[4-(2-hydroxy-3-methacryloy-loxypropyl)-phenyl]propane (Bis-GMA) as the base monomer of dental resin. After mixing with reactive diluent triethyleneglycol dimethacrylate (TEGDMA), fluorinated dimethacrylate (FDMA)/TEGDMA was prepared and compared with Bis-GMA/TEGDMA in physicochemical properties, such as double bond conversion (DC), volumetric shrinkage (VS), water sorption (WS) and solubility (WSL), flexural strength (FS) and modulus (FM). The results showed that, when compared with Bis-GMA based resin, FDMA-based resin had several advantages, such as higher DC, lower VS, lower WS, and higher FS after water immersion. All of these revealed that FDMA had potential to be used as a substitute for Bis-GMA. Of course, many more studies, such as biocompatibility testing, should be undertaken to prove whether FDMA could be applied in clinic.
机译:为了减少牙科医生对双酚A(BPA)衍生物的接触,合成了一种氟化二甲基丙烯酸酯单体来代替2,2-双[4-(2-羟基-3-甲基丙烯酰基-氧丙基)-苯基]丙烷-GMA)作为牙科树脂的基础单体。与反应性稀释剂三乙二醇二甲基丙烯酸酯(TEGDMA)混合后,制得氟化二甲基丙烯酸酯(FDMA)/ TEGDMA并与Bis-GMA / TEGDMA进行理化性质比较,如双键转化(DC),体积收缩率(VS),吸水率( WS)和溶解度(WSL),抗弯强度(FS)和模量(FM)。结果表明,与Bis-GMA基树脂相比,FDMA基树脂具有多个优点,例如浸入水中后具有较高的DC,较低的VS,较低的WS和较高的FS。所有这些表明,FDMA有潜力被用作Bis-GMA的替代品。当然,应该进行更多的研究,例如生物相容性测试,以证明FDMA是否可以应用于临床。

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