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Quantitative Analysis of Gold Nanoparticles in Single Cells by Laser Ablation Inductively Coupled Plasma-Mass Spectrometry

机译:激光烧蚀电感耦合等离子体质谱法定量分析单细胞中的金纳米颗粒

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Single cell analysis has become an important field of research in recent years reflecting the heterogeneity of cellular responses in biological systems. Here, we demonstrate a new method, based on laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS), which can quantify in situ gold nanoparticles (Au NPs) in single cells. Dried residues of picoliter droplets ejected by a commercial inkjet printer were used to simulate matrix-matched calibration standards. The gold mass in single cells exposed to 100 nM NIST Au NPs (Reference material 8012, 30 nm) for 4 h showed a log-normal distribution, ranging from 1.7 to 72 fg Au per cell, which approximately corresponds to 9 to 370 Au NPs per cell. The average result from 70 single cells (15 ± 13 fg Au per cell) was in good agreement with the result from an aqua regia digest solution of 1.2 × 10~6 cells (18 ± 1 fg Au per cell). The limit of quantification was 1.7 fg Au. This paper demonstrates the great potential of LA-ICPMS for single cell analysis and the beneficial study of biological responses to metal drugs or NPs at the single cell level.
机译:近年来,单细胞分析已成为反映生物系统中细胞应答异质性的重要研究领域。在这里,我们演示了一种基于激光烧蚀电感耦合等离子体质谱(LA-ICPMS)的新方法,该方法可以定量单个细胞中的金纳米颗粒(Au NPs)。由商用喷墨打印机喷射的皮升液滴的干燥残留物用于模拟基质匹配的校准标准品。暴露于100 nM NIST Au NPs(参考材料8012,30 nm)4小时的单个电池中的金质量显示出对数正态分布,范围为每个电池1.7至72 fg Au,大约相当于9至370 Au NPs每个单元格。 70个单细胞(每细胞15±13 fg金)的平均结果与1.2×10〜6细胞的王水消化液(每细胞18±1 fg Au)的结果非常吻合。定量限为1.7 fg金。本文展示了LA-ICPMS在单细胞分析中的巨大潜力以及在单细胞水平上对金属药物或NPs的生物学反应的有益研究。

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