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Measuring in vitro cellular uptake of nanoparticles by transmission electron microscopy

机译:通过透射电子显微镜测量纳米颗粒的体外摄取

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Biomedical application of engineered nanoparticles (NPs) is a growing area of research and development. Uncertainty remains as to the mode of action of many NP types and TEM is a tool capable of addressing this if used in conjunction with standard cellular response assays. We will demonstrate imaging of thin sections of fixed, plastic embedded cells by analytical TEM to identify:superparamagnetic iron oxide NP translocation into cell compartments such as endosomes; amorphous silica NP penetration through a cell membrane without membrane encapsulation and zinc oxide NP degradation in cell compartments. We will then discuss how the in vitro cellular responses to a dose of NPs exposed to cell lines can be correlated to the internalized dose per cell section noting however that quantification of the latter requires random sampling procedures or correlation to higher throughout techniques to measure a population of whole cells. Similarly, analytical TEM measures of NP degradation within intracellular compartments will require a more appropriate sample preparation such as cryo-fixation.
机译:工程纳米粒子(NPS)的生物医学应用是一种日益增长的研发领域。不确定性仍然是许多NP类型和TEM的作用方式,如果与标准蜂窝响应测定结合使用,则TEM是能够解决该工具的工具。我们将通过分析TEM展示固定,塑料嵌入细胞薄部分的成像,以识别:超顺磁性氧化铁NP易位,进入细胞室,例如底皮物;无定形二氧化硅NP穿过细胞膜而没有膜包封和细胞室中的氧化锌NP降解。然后,我们将如何讨论暴露于细胞系的含量的含量的体外细胞反应是如何与每个细胞部分的内化剂量相关,然而,后者的定量需要随机采样程序或与衡量人群的技术更高的相关性或相关性整个细胞。类似地,细胞内隔室内Np降解的分析温度测量将需要更合适的样品制剂如冷冻固定。

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