Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Laboratório de Micologia Aplicada, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
J Med Microbiol. 2021 Jul;70(7). doi: 10.1099/jmm.0.001377.
The presence of biofilms in medical devices is a concerning and important clinical issue for haemodialysis patients who require constant use of prosthetic fistulae and catheters. This prolonged use increases the risk of candidaemia due to biofilm formation. PH151 and clioquinol are 8-hydroxyquinoline derivatives that have been studied by our group and showed interesting anti- activity. This study evaluated the biofilm formation capacity of species on polytetrafluoroethylene (PTFE) and polyurethane (PUR) and investigated the synergistic effects between the compounds PH151 and clioquinol and fluconazole, amphotericin B and caspofungin against biofilm cells removed from those materials. Further, the synergistic combination was evaluated in terms of preventing biofilm formation on PTFE and PUR discs. Susceptibility testing was performed for planktonic and biofilm cells using the broth microdilution method. The checkerboard method and the time-kill assay were used to evaluate the interactions between antifungal agents. Antibiofilm activity on PTFE and PUR materials was assessed to quantify the prevention of biofilm formation. , and showed ability to form biofilms on both materials. By contrast, did not demonstrate this ability. Synergistic interaction was observed when PH151 was combined with fluconazole in 77.8 % of isolates and this treatment was shown to be concentration- and time-dependent. On the other hand, indifferent interactions were predominantly observed with the other combinations. A reduction in biofilm formation on PUR material of more than 50 % was observed when using PH151 combined with fluconazole. PH151 demonstrated potential as a local treatment for use in a combination therapy approach against biofilm formation on haemodialysis devices.
生物膜在医疗器械中的存在是接受血液透析治疗的患者面临的一个重要临床问题,他们需要长期使用人造瘘管和导管。这种长时间的使用会增加因生物膜形成而导致念珠菌血症的风险。PH151 和氯己定是我们小组研究过的 8-羟基喹啉衍生物,具有有趣的抗 活性。本研究评估了 种属在聚四氟乙烯(PTFE)和聚氨酯(PUR)上形成生物膜的能力,并研究了化合物 PH151 和氯己定与氟康唑、两性霉素 B 和卡泊芬净之间的协同作用,针对从这些材料中去除的生物膜细胞。此外,还评估了协同组合在防止 PTFE 和 PUR 圆盘上形成生物膜方面的效果。使用肉汤微量稀释法对浮游细胞和生物膜细胞进行药敏试验。棋盘法和时间杀伤试验用于评估抗真菌药物之间的相互作用。通过评估对 PTFE 和 PUR 材料的抗生物膜活性来量化预防生物膜形成的效果。 和 能够在两种材料上形成生物膜。相比之下, 则没有表现出这种能力。当 PH151 与氟康唑联合使用时,观察到 77.8%的分离株存在协同相互作用,并且这种治疗方法呈浓度和时间依赖性。另一方面,主要观察到其他组合存在无关相互作用。当使用 PH151 联合氟康唑时,PUR 材料上的生物膜形成减少了 50%以上。PH151 显示出作为局部治疗的潜力,可用于针对血液透析设备上 生物膜形成的联合治疗方法。