首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Solubility of epiphany endodontic sealer prepared with resinous solvent.
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Solubility of epiphany endodontic sealer prepared with resinous solvent.

机译:用树脂溶剂制备的顿悟根管封闭剂的溶解性。

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PURPOSE: To evaluate in vitro the solubility of the Epiphany endodontic filling material Epiphany (Pentron Clinical Technologies, Wallingford, CT) prepared with its resinous solvent. METHODS: The specimens were prepared in the following experimental conditions: (1) GI, epiphany without photoactivation; (2) GII, Epiphany prepared with resinous solvent without photoactivation; (3) GIII, Epiphany followed by photoactivation; and (4) GIV, Epiphany prepared with resinous solvent followed by photoactivation. Ten specimens of each group were obtained from Teflon molds with 80% reduction in volume of the specimen's dimensions based on American National Standard Institute/American Dental Association (ANSI/ADA) Specification No. 57. The samples were weighted and immersed in distilled water for 7 days. After this period, they were removed, dried, and weighed again. Solubility was calculated by using samples weight loss (%). The immersion liquid was evaluated through atomic absorption spectrometry. RESULTS: The sealers without photoactivation were statistically similar (p > 0.05) between themselves (GI = 6.93% and GII = 6.39%) and different from the uncured sealers, which were statistically different between themselves (p < 0.05) (GIII = 3.56% and GIV = 0.47%). Only the Epiphany sealer prepared with resinous solvent followed by photoactivation presented solubility values within ANSI/ADA requirements, liberating the following amounts of ions: 114.43 microg of Ca(2+)/mL, 2.4 microg of Mg(2+)/mL, 0.33 microg of Fe(2+)/mL, 0.11 microg of Zn(2+)/mL, 1.31 microg of Ni(2+)/mL, and 7.1 microg of Na(+)/mL. CONCLUSION: The association of resinous solvent to the Epiphany sealer followed by photoactivation resulted in a filling material with low solubility and expressive liberation of calcium ions.
机译:目的:在体外评估使用树脂溶剂制备的Epiphany牙髓牙髓充填材料Epiphany(Pentron Clinical Technologies,Wallingford,CT)的溶解度。方法:在以下实验条件下制备标本:(1)胃肠道,顿悟,无光活化; (2)GII,主显节,用树脂溶剂制备,未进行光活化; (3)GIII,顿悟,随后进行光活化; (4)GIV,用树脂溶剂制备的顿悟,随后进行光活化。根据美国国家标准协会/美国牙科协会(ANSI / ADA)规范No.57,从特氟龙模具中获得的每组十个样品的体积减小了80%。将样品称重并浸入蒸馏水中,以备不时之需。 7天。在这段时间之后,将它们取出,干燥并再次称重。通过使用样品重量损失(%)计算溶解度。通过原子吸收光谱法评价浸渍液。结果:没有光活化作用的封闭剂之间的统计学差异(p> 0.05)(GI = 6.93%,GII = 6.39%),与未固化的封闭剂之间存在统计学差异(p <0.05)(GIII = 3.56%)和GIV = 0.47%)。只有用树脂溶剂制备并进行光活化的Epiphany密封剂才显示出ANSI / ADA要求的溶解度值,释放出以下离子量:114.43微克Ca(2 +)/ mL,2.4微克Mg(2 +)/ mL,0.33微克的Fe(2 +)/ mL,0.11微克的Zn(2 +)/ mL,1.31微克的Ni(2 +)/ mL和7.1微克的Na(+)/ mL。结论:树脂溶剂与Epiphany密封剂缔合,然后进行光活化,导致填充材料的溶解度低,且钙离子的表达自由。

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