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Synergistic Antifungal Study of PEGylated Graphene Oxides and Copper Nanoparticles against Candida albicans

机译:聚乙二醇化氧化石墨烯和铜纳米颗粒对白色念珠菌的协同抗真菌研究

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摘要

The coupling reactions of polyethylene glycol (PEG) with two different nano-carbonaceous materials, graphene oxide (GO) and expanded graphene oxide (EGO), were achieved by amide bond formations. These reactions yielded PEGylated graphene oxides, GO-PEG and EGO-PEG. Whilst presence of the newly formed amide links (NH-CO) were confirmed by FTIR stretches observed at 1732 cm and 1712 cm , the associated Raman D- and G-bands resonated at 1311/1318 cm and 1584/1595 cm had shown the carbonaceous structures in both PEGylated products remain unchanged. Whilst SEM images revealed the nano-sheet structures in all the GO derivatives (GO/EGO and GO-PEG/EGO-PEG), TEM images clearly showed the nano-structures of both GO-PEG and EGO-PEG had undergone significant morphological changes from their starting materials after the PEGylated processes. The successful PEGylations were also indicated by the change of pH values measured in the starting GO/EGO (pH 2.6–3.3) and the PEGylated GO-PEG/EGO-PEG (pH 6.6–6.9) products. Initial antifungal activities of selective metallic nanomaterials (ZnO and Cu) and the four GO derivatives were screened against using the in vitro cut-well method. Whilst the haemocytometer count indicated GO-PEG and copper nanoparticles (CuNPs) exhibited the best antifungal effects, the corresponding SEM images showed had, respectively, undergone extensive shrinkage and porosity deformations. Synergistic antifungal effects all GO derivatives in various ratio of CuNPs combinations were determined by assessing viabilities using broth dilution assays. The best synergistic effects were observed when a 30:70 ratio of GO/GO-PEG combined with CuNPs, where MIC 185–225 μm/mL were recorded. Moreover, the decreased antifungal activities observed in EGO and EGO-PEG may be explained by their poor colloidal stability with increasing nanoparticle concentrations.
机译:聚乙二醇(PEG)与两种不同的纳米碳质材料,氧化石墨烯(GO)和膨胀的氧化石墨烯(EGO)的偶联反应是通过酰胺键形成而实现的。这些反应产生了聚乙二醇化的氧化石墨烯,GO-PEG和EGO-PEG。虽然通过在1732 cm和1712 cm处观察到FTIR拉伸证实了新形成的酰胺键(NH-CO)的存在,但在1311/1318 cm和1584/1595 cm处共振的相关拉曼D波段和G波段显示出碳质两种聚乙二醇化产物中的结构保持不变。 SEM图像显示了所有GO衍生物(GO / EGO和GO-PEG / EGO-PEG)的纳米片结构,而TEM图像清楚地表明GO-PEG和EGO-PEG的纳米结构均发生了明显的形态变化从聚乙二醇化工艺后的原料中提取。起始GO / EGO(pH 2.6-3.3)和PEG化GO-PEG / EGO-PEG(pH 6.6-6.9)产品中测得的pH值变化也表明成功的PEG化。使用体外切阱法筛选了选择性金属纳米材料(ZnO和Cu)和四种GO衍生物的初始抗真菌活性。血细胞计数器显示GO-PEG和铜纳米颗粒(CuNPs)表现出最佳的抗真菌作用,而相应的SEM图像则分别显示出较大的收缩率和孔隙率变形。协同抗真菌作用通过使用肉汤稀释试验评估活力,确定了各种比例的CuNPs组合中的所有GO衍生物。当GO / GO-PEG与CuNPs的比例为30:70时,观察到最佳的协同作用,记录的MIC 185-225μm/ mL。此外,在EGO和EGO-PEG中观察到的抗真菌活性下降可能是由于随着纳米粒子浓度的增加,它们的胶体稳定性差。

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