首页> 美国卫生研究院文献>Journal of Fungi >Eradication of Candida albicans Biofilm Viability: In Vitro Combination Therapy of Cationic Carbosilane Dendrons Derived from 4-Phenylbutyric Acid with AgNO3 and EDTA
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Eradication of Candida albicans Biofilm Viability: In Vitro Combination Therapy of Cationic Carbosilane Dendrons Derived from 4-Phenylbutyric Acid with AgNO3 and EDTA

机译:消除念珠菌蛋白生物膜活力:阳离子碳硅烷树枝状体外组合治疗衍生自4-苯基丁酸与AgNO3和EDTA

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摘要

Candida albicans is a human pathogen of significant clinical relevance. This pathogen is resistant to different drugs, and most clinical antifungals are not effective against the prevention and treatment of C. albicans infections. As with other microorganisms, it can produce biofilms that serve as a barrier against antifungal agents and other substances, contributing to infection in humans and environmental tolerance of this microorganism. Thus, resistances and biofilm formation make treatment difficult. In addition, the complete eradication of biofilms in implants, catheters and other medical devices, is challenging and necessary to prevent relapses of candidemia. Therefore, it is a priority to find new molecules or combinations of compounds with anti-Candida biofilm activity. Due to the difficulty of treating and removing biofilms, the aim of this study was to evaluate the in vitro ability of different generation of cationic carbosilane dendrons derived from 4-phenylbutyric acid, ArCO2Gn(SNMe3I)m, to eradicate C. albicans biofilms. Here, we assessed the antifungal activity of the second generation dendron ArCO2G2(SNMe3I)4 against C. albicans cells and established biofilms since it managed to seriously damage the membrane. In addition, the combinations of the second generation dendron with AgNO3 or EDTA eradicated the viability of biofilm cells. Alterations were observed by scanning electron microscopy and cytotoxicity was assessed on HeLa cells. Our data suggest that the dendritic compound ArCO2G2(SNMe3I)4 could represent an alternative to control the infections caused by this pathogen.
机译:白色念珠菌是显著的临床意义的人类病原体。这种病原体是不同的药物产生耐药性,而且大多数临床抗真菌药物不反对白色念珠菌感染的预防和治疗效果。如同其它微生物,它可以产生充当针对抗真菌剂和其他物质的屏障,在人类和该微生物的环境耐受性促进感染生物膜。因此,电阻和生物膜的形成使治疗难度。此外,植入物,导管等医疗器械,生物膜彻底根除是具有挑战性的和必要的预防念珠菌的复发。因此,寻找新的分子或与抗念珠菌生物膜活性的化合物的组合的优先级。由于治疗和去除生物膜的难度,本研究的目的是评估不同代从4-苯基丁酸,ArCO2Gn(SNMe3I)米得到的阳离子型的碳硅烷树状分子的体外能力,消除白色念珠菌生物膜。在这里,我们评估了第二代树枝状大分子ArCO2G2(SNMe3I)4对白色念珠菌细胞的抗真菌活性和已建立的生物膜,因为它成功地严重损坏该膜。此外,用AgNO 3或EDTA的第二代树枝状大分子的组合根除生物膜细胞的生存能力。变化是由扫描电子显微镜观察到和细胞毒性对HeLa细胞中评估。我们的数据表明,该化合物的树突ArCO2G2(SNMe3I)4可以表示一个替代来控制所造成的这种病原体的感染。

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