首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Analytical characterization of gold nanoparticle primary particles, aggregates, agglomerates, and agglomerated aggregates
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Analytical characterization of gold nanoparticle primary particles, aggregates, agglomerates, and agglomerated aggregates

机译:金纳米粒子一次颗粒,聚集体,团聚体和团聚聚集体的分析表征

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Gold nanoparticles have been studied for many biomedical applications. However, alterations in the gold nanoparticles' environment frequently lead to the formation of aggregates and agglomerates, which have not been well characterized. These new structures could significantly change the biological impact of the nanoparticles, so the appropriate characterization of these structures prior to biological administration is vital for the correct interpretation of toxicology results. By varying the solvent or heating under pressure, four reproducible gold nanoparticles structures were created: 10 nm primary particles, aggregates of the primary particles that contain non-reversible bonds between the individual nanoparticles, agglomerates of primary particles that contain reversible interactions between the individual nanoparticles, and agglomerated aggregates that have reversible bonds linking individual aggregates. Ultraviolet-visible (UV-Vis) spectroscopy, thermal gravitational analysis, and neutron activation analysis were each found to accurately measure the concentration of the primary particles. The primary particles measured 10 nm by dynamic light scattering (DLS) and had a spherical morphology by transmission electron microscopy (TEM) while the aggregates measured 110 nm by DLS and had a distorted morphology by TEM. The agglomerate and aggregated agglomerate samples both measured >1,000 nm by DLS, but the individual particles had significantly different morphologies by TEM. Multiple other analytical techniques, including ultracentrifugation, gel electrophoresis, and X-ray diffraction, also showed unique traits for each structure. The structural differences did not change in the presence of cell culture media or rat serum. In addition, the primary particles, aggregates, and agglomerates each had a unique UV-Vis spectrum, allowing for an inexpensive, rapid method to differentiate between the structures.(outside the USA).
机译:金纳米颗粒已被研究用于许多生物医学应用。然而,金纳米颗粒环境的改变经常导致聚集体和附聚物的形成,这尚未得到很好的表征。这些新结构可能会显着改变纳米颗粒的生物学影响,因此在生物给药之前对这些结构进行适当的表征对于正确解释毒理学结果至关重要。通过改变溶剂或在压力下加热,创建了四个可重现的金纳米粒子结构:10 nm初级粒子,包含各个纳米粒子之间不可逆键的初级粒子的聚集体,包含各个纳米粒子之间可逆相互作用的初级粒子的聚集体,以及具有可逆键连接各个聚集体的聚集聚集体。紫外可见(UV-Vis)光谱,热引力分析和中子活化分析均被发现可以准确地测量初级粒子的浓度。初级粒子通过动态光散射(DLS)测量为10 nm,通过透射电子显微镜(TEM)测量为球形,而聚集体通过DLS测量为110 nm,并且通过TEM畸变。通过DLS测得的团聚体和聚集团聚体样品均> 1,000 nm,但单个颗粒的TEM形貌差异显着。多种其他分析技术,包括超速离心,凝胶电泳和X射线衍射,也显示出每种结构的独特特征。在细胞培养基或大鼠血清存在下,结构差异没有改变。此外,初级粒子,聚集体和附聚物各自具有独特的UV-Vis光谱,从而提供了一种廉价,快速的方法来区分结构(美国以外)。

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