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单细胞纳米颗粒浓度的定量及其在细胞群体中的分布。

Quantification of single-cell nanoparticle concentrations and the distribution of these concentrations in cell population.

机构信息

Department of Biomedical Engineering, Stony Brook University, , Stony Brook, NY 11794-5281, USA.

出版信息

J R Soc Interface. 2014 Feb 19;11(94):20131152. doi: 10.1098/rsif.2013.1152. Print 2014 May 6.

Abstract

Quantification of nanoparticle uptake into cells is necessary for numerous applications in cellular imaging and therapy. Herein, synchrotron X-ray fluorescence (SXRF) microscopy, a promising tool to quantify elements in plant and animal cells, was employed to quantify and characterize the distribution of titanium dioxide (TiO2) nanosphere uptake in a population of single cells. These results were compared with average nanoparticle concentrations per cell obtained by widely used inductively coupled plasma mass spectrometry (ICP-MS). The results show that nanoparticle concentrations per cell quantified by SXRF were of one to two orders of magnitude greater compared with ICP-MS. The SXRF results also indicate a Gaussian distribution of the nanoparticle concentration per cell. The results suggest that issues relevant to the field of single-cell analysis, the limitation of methods to determine physical parameters from large population averages leading to potentially misleading information and the lack of any information about the cellular heterogeneity are equally relevant for quantification of nanoparticles in cell populations.

摘要

纳米颗粒进入细胞的定量对于细胞成像和治疗的许多应用是必要的。本文采用同步辐射 X 射线荧光(SXRF)显微镜,这是一种有望定量植物和动物细胞中元素的工具,来定量和表征在单细胞群体中二氧化钛(TiO2)纳米球摄取的分布。这些结果与通过广泛使用的电感耦合等离子体质谱法(ICP-MS)获得的每个细胞的平均纳米颗粒浓度进行了比较。结果表明,通过 SXRF 定量的每个细胞的纳米颗粒浓度比 ICP-MS 高一个到两个数量级。SXRF 结果还表明,每个细胞的纳米颗粒浓度呈高斯分布。结果表明,与单细胞分析领域相关的问题、从大的群体平均值确定物理参数的方法的局限性导致潜在的误导信息,以及缺乏关于细胞异质性的任何信息,对于细胞群体中纳米颗粒的定量同样重要。

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