Department of Prosthodontics, Bauru School of Dentistry, University of São Paulo, Bauru, Brazil.
Department of Dentistry, State University of Ponta Grossa, Ponta Grossa, Brazil.
J Prosthodont. 2018 Feb;27(2):177-181. doi: 10.1111/jopr.12660. Epub 2017 Nov 14.
To investigate the ultimate tensile strength of temporary soft denture liners modified by minimum inhibitory concentrations (MICs) of antifungal agents for Candida albicans biofilm (SC5314) determined in previous microbiological research.
Dumbbell-shaped specimens (n = 7) with a central cross-sectional area of 6 × 3 × 33 mm were produced by Softone and Trusoft, without (control) or with incorporation of drugs in powder form at MICs for C. albicans biofilm (per g of material powder): nystatin (0.032 g), chlorhexidine diacetate (0.064 g), ketoconazole (0.128 g), miconazole (0.256 g), and itraconazole (0.256 g). After plasticization, specimens were immersed in distilled water at 37°C for 24 hours, 7 or 14 days, and then tested in tension in a universal testing machine at 40 mm/min. Data of tensile strength (MPa) and elongation percentage (%) were submitted to 3-way ANOVA and Tukey's test (α = 0.05).
At the end of 14 days, the tensile strength for both materials was significantly lower in the groups modified by miconazole and itraconazole compared to the other groups (p < 0.0001), which showed no significant difference between them (p > 0.05). After 7 and 14 days in water, miconazole and itraconazole added into both materials resulted in significantly lower elongation percentages compared to the other antifungal agents and control (p < 0.0001), which were similar to each other (p > 0.05).
The addition of the nystatin, chlorhexidine, and ketoconazole at MICs for C. albicans biofilm resulted in no harmful effects on the tensile strength and elongation percentage of the temporary soft denture liner materials up to 14 days.
研究先前微生物研究中确定的抗真菌药物对白念珠菌生物膜(SC5314)最低抑菌浓度(MIC)改性的临时软衬材料的极限拉伸强度。
用 Softone 和 Trusoft 制作哑铃形试件(n = 7),中央横截面积为 6×3×33mm,无(对照)或粉末形式加入药物,药物浓度为白念珠菌生物膜的 MIC(每克材料粉末):制霉菌素(0.032g)、醋酸氯己定(0.064g)、酮康唑(0.128g)、咪康唑(0.256g)和伊曲康唑(0.256g)。塑化后,试件在 37°C 蒸馏水中浸泡 24 小时、7 天或 14 天,然后在万能试验机上以 40mm/min 的速度进行拉伸测试。拉伸强度(MPa)和伸长率(%)的数据进行 3 因素方差分析和 Tukey 检验(α=0.05)。
在第 14 天,与其他组相比,两种材料中添加咪康唑和伊曲康唑的组的拉伸强度明显较低(p<0.0001),且它们之间无显著差异(p>0.05)。在水中浸泡 7 天和 14 天后,与其他抗真菌药物和对照组相比,添加到两种材料中的咪康唑和伊曲康唑导致伸长率明显降低(p<0.0001),但彼此相似(p>0.05)。
在白念珠菌生物膜的 MIC 下添加制霉菌素、氯己定和酮康唑对临时软衬材料的拉伸强度和伸长率没有不良影响,在 14 天内没有不良影响。