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Structural analysis of soft multicomponent nanoparticle clusters

机译:软多组分纳米颗粒簇的结构分析

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Quantitative techniques are essential to analyze the structure of soft multicomponent nanobioclusters. Here, we combine electrospray differential mobility analysis (ES-DMA), which rapidly measures the size of the entire cluster, with transmission electron microscopy (TEM), which detects the hard components, to determine the presence and composition of the softer components. Coupling analysis of TEM and ES-DMA derived data requires the creation and use of analytical models to determine the size and number of constituents in nanoparticle complexes from the difference between the two measurements. Previous ES-DMA analyses have been limited to clusters of identical spherical particles. Here, we dramatically extend the ES-DMA analysis framework to accommodate more challenging geometries, including protein corona-coated nanorods, clusters composed of heterogeneously sized nanospheres, and nanobioclusters composed of both nanospheres and nanorods. The latter is critical to determining the number of quantum dots attached to lambda () phage, a key element of a rapid method to detect bacterial pathogens in environmental and clinical samples.
机译:定量技术对于分析软多组分纳米生物簇的结构至关重要。在这里,我们将电喷雾差分迁移率分析(ES-DMA)和透射电子显微镜(TEM)结合起来,这些分析可快速测量整个簇的大小,透射电子显微镜(TEM)可检测硬组分,从而确定较软组分的存在和组成。 TEM和ES-DMA衍生数据的耦合分析需要创建和使用分析模型,以便根据两次测量之间的差异来确定纳米粒子复合物中成分的大小和数量。以前的ES-DMA分析仅限于相同球形颗粒的簇。在这里,我们极大地扩展了ES-DMA分析框架,以适应更具挑战性的几何结构,包括蛋白电晕涂层纳米棒,由大小不一的纳米球组成的簇以及由纳米球和纳米棒组成的纳米生物簇。后者对于确定附着在λ()噬菌体上的量子点的数量至关重要,λ是噬菌体快速检测环境和临床样品中细菌病原体方法的关键要素。

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