Programa de Pós-Graduação em Microbiologia Agrícola e do Ambiente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Laboratório de Micologia Aplicada, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Braz J Microbiol. 2020 Sep;51(3):1037-1049. doi: 10.1007/s42770-020-00242-z. Epub 2020 Feb 19.
Infections associated with medical devices are often related to colonization by Candida spp. biofilm; in this way, numerous strategies have been developed and studied, mainly in order to prevent this type of fungal growth.
Considering the above, the main objective of the present study is to make a rational choice of the best antifungal therapy for the in vitro treatment of the biofilm on venous catheters, proposing an innovative formulation of a film-forming system to coat the surface in order to prevent the formation of biofilms.
Anidulafungin, fluconazole, voriconazole, ketoconazole, amphotericin B, and the association of anidulafungin and amphotericin B were tested against biofilms of C. albicans, C. tropicalis, and C. parapsilosis strains in microtiter plates and in a polyurethane catheter. Besides, anidulafungin, amphotericin B, and the combination of both were incorporated in a film-forming system and were evaluated against biofilm.
The superior activity of anidulafungin was demonstrated in relation to the other antifungal agents. Although amphotericin B showed good activity, high concentrations were required. The combination showed a synergistic action, in solution and in the formulation, showing excellent results, with activity above 90%.
Due to the superiority of anidulafungin and the synergistic activity of the combination, these alternatives were the most promising options for use in a formulation proposal as a new strategy to combat the Candida spp. biofilm. These formulations demonstrated high in vitro performance in the prevention of biofilms, indicating that they are candidates with great potential for in vivo tests.
与医疗器械相关的感染通常与念珠菌属生物膜的定植有关;为此,已经开发和研究了许多策略,主要是为了预防这种真菌生长。
鉴于上述情况,本研究的主要目的是为体外治疗静脉导管生物膜选择最佳抗真菌治疗方法,提出一种创新的成膜系统配方,以涂覆表面,从而防止生物膜的形成。
在微量滴定板和聚氨酯导管中,对白色念珠菌、热带念珠菌和近平滑念珠菌的生物膜进行了安尼拉fungin、氟康唑、伏立康唑、酮康唑、两性霉素 B 以及安尼拉fungin 和两性霉素 B 联合治疗的测试。此外,将安尼拉fungin、两性霉素 B 和两者的组合纳入成膜系统,并对生物膜进行了评估。
与其他抗真菌药物相比,安尼拉fungin 的活性更高。尽管两性霉素 B 表现出良好的活性,但需要高浓度。联合用药显示出协同作用,无论是在溶液中还是在配方中,都取得了极好的效果,活性超过 90%。
由于安尼拉fungin 的优越性和联合用药的协同作用,这些替代方案是作为对抗念珠菌属生物膜的新策略在配方建议中最有前途的选择。这些配方在预防生物膜方面表现出了很高的体外性能,表明它们是具有很大体内测试潜力的候选药物。