期刊文献+

从胆酸制备的牙科树脂溶胀性能研究

Sweling and Wettability of Light-Cured Methacrylate-Based Dental Resins Prepared from Cholic Acid
下载PDF
导出
摘要 从胆酸(CA)合成了2’-甲基丙烯酰氧基乙基-3α,7α,12α-三甲基丙烯酰氧基-5β-胆酸 -24-酯(CACE4MA),并应用光聚合方法将其制成了高分子树脂。实验选用商业单体2,2’-二 [4-(2-羟基-3-甲基丙烯酰氧丙氧基)苯基]丙烷(Bis—GMA)作为对比物,三甘醇二甲基丙烯酸酯(TEGDMA)作稀释剂,樟脑醌(CQ)和甲基丙烯酸-2-(二甲氨基)乙酯(DMAEMA)的混合物作引发剂。研究光照时间为60 s的树脂在蒸馏水和0.1 mol/L HCl溶液中的溶胀行为。研究显示,在蒸馏水中CAGE4MA树脂的溶胀值是0.41%,比相同条件下商业单体Bis—GMA (2.04%)和TEGDMA(4.77%)的溶胀值低。CAGE4MA和TEGDMA共聚物的溶胀值随着树脂中TEGDMA含量的增加而增加。 2'-Methacryloyloxyethyl 3α,7α,12α-trimethacryloyloxy -5β-cholan-24-ate (CAGE4MA) has been prepared from cholic acid. Photo-polymeric resins were prepared from CAGE4MA. 2,2-bis [ 4- (2-hydroxy-3-methaerylyloxypropoxy) phenyl propane ( Bis-GMA ) was used for comparison, triethyleneglycol dimethacrylate (TEGDMA) was used as diluent. The polymerization was initiated by camphoroquinone (CQ) / N, N-dimethylaminoethyl methacrylate (DMAEMA) system. The initiated time was 60s. The swelling behaviors of resins in distilled water and 0.1 mol/L HCI solutions were studied. The swelling value of CAGE4MA resin was 0.41% in distilled water, which is much lower than those of bis-GMA resin (2.04%) and TEGDMA resin (4.77%) under the same conditions. Copolymers of CAGE4MA and TEGDMA have been prepared. With the increase of TEGDMA in mixture, the swelling value of CAGE4MA-TEGDMA resins increased.
出处 《天津科技大学学报》 CAS 2005年第4期35-39,共5页 Journal of Tianjin University of Science & Technology
关键词 胆酸 修饰 牙科材料 溶胀性能 cholic acid modification dental material swelling property
  • 相关文献

参考文献16

  • 1[1]Moszner N, Salz U. New developments of polymeric dental composites[J]. Prog. Polym. Sci., 2001,26:535-576.
  • 2[2]Hansel C, Leyhausen G, Mai U E H, Geurtsen W. Effects of various resin composite (co)monomers and extracts on two caries-associated micro-organisms in vitro [ J ]. Dent.Mater, 1998, 77:60-67.
  • 3[3]Spahl W, Budzikicwicz H, Geursten W. Extractable residual monomers from various resin materials-a qualitative study [J]. J. Dent. Res., 1994, 73:295.
  • 4[4]Kalachandra S, Turner D T. Water sorption of polymethacrylate networks: Bis-GMA. TEGDMA copolymers [ J ]. J. Biomed. Mater. Res. , 1987,21:329 -338.
  • 5[5]I. Sideridou V. , Tserki G. Study of water sorption, solubility and modulus of elasticity of light-cured dimethacrylatebased dental resins [ J ]. Biomaterials, 2003,24: 655 - 665.
  • 6[6]Takeyama M, Kashibuchis S, Nakabayashi N, Masuhara E.Studies on dental self-curing resins(17) :adhesion of PMMA with bovine enamel or dental alloys[ J]. J. Jpn. Dent. Appar. Mater., 1978, 19:179-185.
  • 7[7]Yamauchi J, Nakabayashi N, Masuhara E. Adhesive agents for hard tissue containing phosphoric acid monomers [ J ].Am. Chem. Soc. Polym. Preprints, 1979, 20:594-595.
  • 8[8]Winkler M M, Moore B K. Correlation of bond strength with surface roughness using a new roughness measurement technique[J]. Dent. Mater., 1994, 10 : 222 - 229
  • 9[9]ChungC M, Kim J G, Kim M S. Development of a new photocurable composite resin with reduced curing shrinkage[ J]. Dent Mater, 2002, 18:174 - 178.
  • 10[10]Denike J K, Moskova M, Zhu X X. Stereoselective Synthesis of 3β-Bile Acid Derivatives from the 3α-Analog [ J ].Chem. Phys. Lipids., 1995,77:261-267.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部