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制霉菌素与组织调理剂联合使用对其极限拉伸强度的影响。

Effect of the association of nystatin with a tissue conditioner on its ultimate tensile strength.

作者信息

Urban Vanessa Migliorini, de Souza Raphael Freitas, Arrais Cesar Augusto Galvao, Borsato Karina Tostes, Vaz Luís Geraldo

机构信息

Department of Dental Materials and Prosthodontics, Araraquara Dental School, São Paulo State University, Araraquara, São Paulo, Brazil.

出版信息

J Prosthodont. 2006 Sep-Oct;15(5):295-9. doi: 10.1111/j.1532-849X.2006.00130.x.

Abstract

PURPOSE

This study evaluated the ultimate tensile strength of a tissue conditioner without nystatin incorporation (GI-control group) and the same tissue conditioner modified by the addition of nystatin in two concentrations: GII-500,000 International Units (U) and GIII-1,000,000 U, in which each milligram of the medicament corresponded to 6079 U.

MATERIALS AND METHODS

Dumbbell-shaped specimens (N= 7) with a central cross-sectional area of 33 x 6 x 3 mm were produced for the three experimental groups. After polymerization following manufacturer's instructions, specimens were immersed in distilled water at 37 degrees C for either 24 hours or 7 days and then tested in tension in the MTS 810 at 40 mm/minute. Data were analyzed by two-way ANOVA followed by Tukey's test, at 95% level of confidence.

RESULTS

The means (force-grams (gf) +/- standard deviation) of the ultimate tensile strength were: GI-634.29 +/- 122.80; GII-561.92 +/- 133.56; and GIII-547.30 +/- 73.47 for 24-hour storage, and GI-536.68 +/- 54.71; GII-467.50 +/- 143.51; and GIII-500.62 +/- 159.76 for 7-day storage. There were no statistically significant differences among the three experimental groups (p > 0.05). The ultimate tensile strength means of all experimental groups after 7 days were significantly lower than those observed after 24 hours (p= 0.04).

CONCLUSIONS

The results of this study suggest that the addition of nystatin into the tissue conditioner investigated in concentrations below 1,000,000 U did not affect its ultimate tensile strength.

摘要

目的

本研究评估了未添加制霉菌素的组织调理剂(GI对照组)以及添加了两种浓度制霉菌素的相同组织调理剂的极限拉伸强度,这两种浓度分别为:GII - 500,000国际单位(U)和GIII - 1,000,000 U,其中每毫克药物相当于6079 U。

材料与方法

为三个实验组制作了中心横截面积为33×6×3 mm的哑铃形试样(N = 7)。按照制造商的说明进行聚合后,将试样在37℃的蒸馏水中浸泡24小时或7天,然后在MTS 810上以40毫米/分钟的速度进行拉伸测试。数据采用双向方差分析,随后进行Tukey检验,置信水平为95%。

结果

对于24小时储存,极限拉伸强度的平均值(力 - 克(gf)±标准差)分别为:GI - 634.29±122.80;GII - 561.92±133.56;GIII - 547.30±73.47;对于7天储存,分别为:GI - 536.68±54.71;GII - 467.50±143.51;GIII - 500.62±159.76。三个实验组之间无统计学显著差异(p>0.05)。所有实验组7天后的极限拉伸强度平均值显著低于24小时后的观察值(p = 0.04)。

结论

本研究结果表明,在低于1,000,000 U的浓度下向所研究的组织调理剂中添加制霉菌素不会影响其极限拉伸强度。

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