Zago Patrícia Maria Wiziack, Dos Santos Castelo Branco Simeone Júlio, de Albuquerque Bogéa Fecury Letícia, Carvalho Letícia Torres, Rocha Cláudia Quintino, Madeira Petrus Levid Barros, de Sousa Eduardo Martins, de Siqueira Fabiana Suelen Figuerêdo, Paschoal Marco Aurélio Benini, Diniz Rafael Soares, Gonçalves Letícia Machado
Department of Medicine, São Leopoldo Mandic Faculty, Araras, Brazil.
Department of Dentistry, Post-Graduate Program in Dentistry, CEUMA University, São Luís, Brazil.
Front Microbiol. 2019 Aug 13;10:1724. doi: 10.3389/fmicb.2019.01724. eCollection 2019.
Considering the challenge to control -associated denture stomatitis, the search for antifungal substances derived from natural sources has become a trend in the literature. In this study the following effects of extract (CAE) were investigated: action against biofilms of , its cytotoxic potential, and changes caused in acrylic resin. The CAE was characterized by High Performance Liquid Chromatography (HPLC). The susceptibility of to CAE was investigated by Minimum Inhibitory Concentration and Minimum Fungicidal Concentration (MIC and MFC) tests. Acrylic resin disks were fabricated, and biofilms were developed on these for 48 h. Afterward the disks were immersed for 10 min in: PBS (Negative Control); 1% Sodium Hypochlorite (1% SH, Positive Control) or CAE at MIC or 5xMIC. The biofilms were investigated relative to counts and metabolic activity. The cytotoxic potential in keratinocytes and fibroblasts was verified by MTT test. Change in color and roughness of the acrylic resin was analyzed after 28 days of immersion in CAE. The data were analyzed by the ANOVA considering a 5% level of significance. The main compounds detected by HPLC were kaempferol and quercetin. Both MIC and MFC obtained the value of 0.25 mg/mL. The MIC was sufficient to significantly reduce the counts and activity of the biofilm cells ( < 0.0001), while 5xMIC resulted in almost complete eradication, similar to 1% SH. Keratinocytes and fibroblasts exposed to the MIC and 5xMIC presented cell viability similar to that of the Control Group ( > 0.05). No important changes in acrylic resin color and roughness were detected, even after 28 days. It could be concluded that the immersion of acrylic resin in extract in its minimum inhibitory concentration was effective for the reduction of biofilms without any evidence of cytotoxic effects or changes in roughness and color of this substrate.
考虑到控制义齿性口炎的挑战,从天然来源寻找抗真菌物质已成为文献中的一种趋势。在本研究中,对提取物(CAE)的以下作用进行了研究:对白色念珠菌生物膜的作用、其细胞毒性潜力以及对丙烯酸树脂造成的变化。通过高效液相色谱法(HPLC)对CAE进行了表征。通过最低抑菌浓度和最低杀菌浓度(MIC和MFC)试验研究了白色念珠菌对CAE的敏感性。制作了丙烯酸树脂圆盘,并在其上培养白色念珠菌生物膜48小时。之后,将圆盘在以下溶液中浸泡10分钟:PBS(阴性对照);1%次氯酸钠(1% SH,阳性对照)或MIC或5xMIC浓度的CAE。对生物膜的数量和代谢活性进行了研究。通过MTT试验验证了对角质形成细胞和成纤维细胞的细胞毒性潜力。在CAE中浸泡28天后,分析了丙烯酸树脂的颜色和粗糙度变化。采用方差分析对数据进行分析,显著性水平为5%。通过HPLC检测到的主要化合物为山奈酚和槲皮素。MIC和MFC均达到0.25 mg/mL的值。MIC足以显著减少生物膜细胞的数量和活性(P < 0.0001),而5xMIC导致几乎完全根除,类似于1% SH。暴露于MIC和5xMIC的角质形成细胞和成纤维细胞的细胞活力与对照组相似(P > 0.05)。即使在28天后,也未检测到丙烯酸树脂颜色和粗糙度的重要变化。可以得出结论,将丙烯酸树脂浸泡在其最低抑菌浓度的提取物中对减少白色念珠菌生物膜有效,且没有任何细胞毒性作用或该基质粗糙度和颜色变化的证据。