首页> 外文期刊>Assay and drug development technologies >Antifungal Activity of Capric Acid, Nystatin, and Fluconazole and Their In Vitro Interactions Against Candida Isolates from Neonatal Oral Thrush
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Antifungal Activity of Capric Acid, Nystatin, and Fluconazole and Their In Vitro Interactions Against Candida Isolates from Neonatal Oral Thrush

机译:癸酸,黑斯坦和氟康唑的抗真菌活性及其对新生儿口腔鹅口疮的念珠菌分离株的体外相互作用

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Due to the increasing resistance of various Candida species to azole drugs, particularly fluconazole, it would be of significant importance to look for alternative therapies. The aim of this study was to investigate the antifungal activity of capric acid and its in vitro interactions with nystatin and fluconazole against Candida isolates. A total of 40 Candida isolates (C. albicans, 36; C. kefyr, 2; C. tropicalis, 1; C. glabrata, 1) collected from the oral cavity of neonates with oropharyngeal candidiasis and a reference strain of C. albicans (ATCC 10231) were used in this study. Antifungal activity of capric acid and two comparator antifungal drugs, namely fluconazole and nystatin, was tested according to CLSI M27-A3/M60 method. The in vitro interaction between capric acid with fluconazole and nystatin was determined following a checkerboard method and results were interpreted using fractional inhibitory concentration index. Nystatin had the lowest minimum inhibitory concentrations (range, 0.125-8 mu g/mL; geometric mean [GM], 0.6229 mu g/mL) followed by fluconazole (range, 0.5-16 mu g/mL; GM, 1.9011 mu g/mL) and capric acid (range, 128-2,048 mu g/mL; GM, 835.9756 mu g/mL). When tested in combination, capric acid with fluconazole demonstrated synergistic, indifferent, and antagonistic interactions in 3 (7.317%), 24 (58.536%), and 14 (34.146%) cases, respectively. For combination of capric acid with nystatin, synergistic, indifferent, and antagonistic interactions were observed in 1 (2.439%), 19 (46.341%), and 21 (51.219%) cases, respectively. All cases of synergistic interactions were against resistant or susceptible dose-dependent isolates. Fluconazole, nystatin, and capric acid seem to be more effective when they are used alone compared with their combination. However, their combination might be effective on resistant isolates.
机译:由于各种念珠菌物种对唑类药物,特别是氟康唑的抗性越来越大,因此可以重视寻找替代疗法。本研究的目的是研究癸酸的抗真菌活性及其与丹顿和氟康唑对念珠菌分离株的体外相互作用。共有40个念珠菌(C. albicans,36; C.Kefyr,2; C.Tropicalis,1; C.Glabrata,1)从NeoNnate的口腔腔内收集的口咽念珠菌病和C. albicans的参考菌株(在本研究中使用了ATCC 10231。根据CLSI M27-A3 / M60方法测试癸酸和两种比较剂抗真菌药物,即氟康唑和黑斯坦蛋白的抗真菌活性。在棋盘方法后测定癸酸与氟康唑和乳腺素之间的体外相互作用,并使用分数抑制浓度指数解释结果。 Nystatin具有最低最小抑制浓度(范围,0.125-8μg/ ml;几何平均值[gm],0.6229μg/ ml),然后是氟康唑(范围,0.5-16μg/ ml; gm,1.9011 mu g / ml)和癸酸(范围,128-2,048 mu g / ml; gm,835.9756 mu g / ml)。当组合测试时,具有氟康唑的癸酸分别显示出协同,无动点和3(7.317%),24(58.536%)和14例(34.146%)病例的拮抗相互作用。为了分别在1(2.439%),19(46.341%)和21例(51.219%)和21例中观察到癸酸的癸酸的组合,协同,难以置动的和拮抗相互作用。所有协同相互作用的病例都是针对抗性或易感剂的剂量依赖性分离物。氟康唑,黑斯坦和癸酸似乎在单独使用它们与它们的组合相比时更有效。然而,它们的组合可能有效地在抗性隔离物中。

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