首页> 外文期刊>Journal of investigative and clinical dentistry. >Post-antifungal effect and adhesion to buccal epithelial cells of oral Candida dubliniensis isolates subsequent to limited exposure to amphotericin B, ketoconazole and fluconazole
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Post-antifungal effect and adhesion to buccal epithelial cells of oral Candida dubliniensis isolates subsequent to limited exposure to amphotericin B, ketoconazole and fluconazole

机译:后抗真菌效应和对口腔念珠菌上皮细胞的粘附性,在接触两性霉素B,酮烷唑和氟康唑的情况下随后的分离物

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Aim: The post-antifungal effect (PAFE) of Candida and its adherence to oral mucosal surfaces are important determinants of candidal pathogenicity. Candida dubliniensis is allied with recurrent oral candidosis. Oral candidosis can be treated with amphotericin B, ketoconazole and fluconazole. There is no information on the PAFE and its impact on adhesion to oral buccal epithelial cells (BEC) of oral C. dubliniensis isolates. Therefore, the main objective was to reconnoiter the PAFE and adhesion to BEC of 20 C. dubliniensis isolates following brief exposure to aforementioned antimycotics. Methods: After determining the minimum inhibitory concentration (MIC), C. dubliniensis isolates were exposed to sub-lethal concentrations of these drugs for 1 h. Following subsequent drug removal, the PAFE and adhesion to BEC, was determined by a turbidometric method, and an adhesion assay, respectively. Results: Minimum inhibitory concentration (μg/mL) to amphotericin B, ketoconazole and fluconazole, ranged from 0.002 to 0.125, 0.002 to 0.012 and 0.016 to 0.38, respectively. Amphotericin B and ketoconazole induced mean PAFE (hours) were 2.21 and 0.6, respectively. Fluconazole failed to produce a detectable PAFE. Compared to controls, amphotericin B, ketoconazole and fluconazole suppressed the ability to adhere to BEC with a mean percentage reduction of 74.31%, 49.80% (P < 0.0001) and 29.36% (P < 0.05), respectively. Conclusions: Brief exposure to sub-lethal concentrations of aforementioned drugs would exert an antifungal effect by modifying the growth and adhesion of C. dubliniensis isolates.
机译:目的:念珠菌的后抗真菌效应(PAFE)及其对口腔粘膜表面的粘附是候选致病性的重要决定因素。 Candida Dubliniensis与经常性口头患者均联盟。可以用两性霉素B,酮康唑和氟康唑治疗口头患者。没有关于PAFE的信息及其对口腔C. Dubliniensis分离株的口腔颊肌上皮细胞(BEC)的粘附性。因此,主要目的是在短暂暴露于上述抗炎症之后将施用缩略率和粘附到20℃。Dubliniensis分离物。方法:在确定最小抑制浓度(MIC)中,将D.3.30Bliniensis分离物暴露于这些药物的亚致死浓度1小时。在随后的药物去除后,通过浊度方法和粘附测定法测定敷料和对BEC的粘附性。结果:对两性霉素B,酮酮蛋白和氟康唑的最小抑制浓度(μg/ ml),范围为0.002至0.125,0.002至0.012和0.016至0.38。两性霉素B和酮烷酶诱导平均敷蛋白酶(小时)分别为2.21和0.6。氟康唑未能产生可检测的封面。与对照相比,两性霉素B,酮酰脲和氟康唑抑制了粘附到BEC的能力,平均百分比分别减少74.31%,49.80%(P <0.0001)和29.36%(P <0.05)。结论:通过改变C. Dubliniensis分离株C. Dubliniensis分离株的生长和粘附来短暂暴露于上述药物的亚致死浓度。

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