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Synthesis and characterization of ladder structured ormocer resin of siloxane backbone and methacrylate side chain

机译:硅氧烷主链和甲基丙烯酸酯侧链梯形结构树脂的合成与表征

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Available resin-based hard tissue restorations are highly influenced by the problems associated with post-polymerization shrinkage and toxicity of uncured monomers. To address this scenario, we have synthesized an ormocer resin (LSM) of inorganic siloxane backbone using the monomer 3-(trimethoxy silyl)propyl methac-rylate (3-TMSPM) by modified sol gel method. The synthesized polycondensed LSM resin is fashioned with three-dimensional network of ladder structured Si-O-Si backbone which grow continuously to form higher molecular weight (Mn-18956 KDa) prepolymer. Four membered siloxane rings along with intact methacrylates constituted the monomeric unit of the prepolymer LSM. High thermal stability indicated the presence of intense siloxane network whereas low glass transition temperature and melting peak demonstrated the flexibility and partial crystallinity of the LSM resin. Low linear polymerization shrinkage (LPS) of cured LSM resin (0.422 +/- 0.04) witnessed the presence of inorganic siloxane backbone and performed better than cured bisphenol glycidyl methacrylate (BisGMA)composite (0.916 +/- 0.09). Non-cytotoxicity and cytocompatibility of the cured LSM resin proved the eligibility of the resin for hard tissue restorative applications.
机译:现有的基于树脂的硬组织修复体受到与聚合后收缩和未固化单体毒性相关的问题的高度影响。为了解决这种情况,我们通过改良的溶胶凝胶法,使用单体3-(三甲氧基甲硅烷基)丙基甲基丙烯酸酯(3-TMSPM)合成了无机硅氧烷主链的ormocer树脂(LSM)。合成的缩聚LSM树脂采用梯形结构的Si-O-Si骨架三维网络,不断生长形成更高分子量(Mn-18956 KDa)的预聚物。四元硅氧烷环与完整的甲基丙烯酸酯一起构成了预聚物LSM的单体单元。高热稳定性表明存在强烈的硅氧烷网络,而低玻璃化转变温度和熔融峰表明LSM树脂具有柔韧性和部分结晶性。固化LSM树脂的低线性聚合收缩率(LPS)(0.422 +/- 0.04%)见证了无机硅氧烷主链的存在,并且性能优于固化的双酚缩水甘油甲基丙烯酸酯(BisGMA)复合材料(0.916 +/- 0.09%)。固化的LSM树脂的无细胞毒性和细胞相容性证明了该树脂适用于硬组织修复应用。

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