CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
Beijing Metallomics Facility and CAS-HKU Joint Laboratory of Metallomics on Health and Environment, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
Anal Chem. 2020 Nov 3;92(21):14339-14345. doi: 10.1021/acs.analchem.0c01775. Epub 2020 Oct 12.
Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) is an emerging method for the analysis of metal nanoparticles (NPs) in single cells. However, two main obstacles, low analytical throughput and lack of commercial reference materials, need to be overcome. In this work, we demonstrated the principles of a new approach termed "single-cell isotope dilution analysis" (SCIDA) to remove the two obstacles. For a proof of concept, macrophage cells were chosen as a model to study the uptake of silver NPs (AgNPs) at a single-cell level. Single cells exposed to AgNPs were placed in an array by a microfluidic technique; each cell in the array was precisely dispensed with a known picoliter droplet of an enriched isotope solution with a commercial inkjet printer; accurate quantification of AgNPs in single cells was done by using isotope dilution LA-ICP-MS. The average Ag mass of 1100 single cells, 396 ± 219 fg Ag per cell, was in good accord with the average of the population of cells determined by solution ICP-MS analysis. The detection limit was 0.2 fg Ag per cell. The SCIDA approach is expected to be widely applied for the study of cell-NP interactions and biological effects of NPs at the single-cell level.
激光烧蚀-电感耦合等离子体质谱法(LA-ICP-MS)是一种新兴的分析单细胞中金属纳米颗粒(NPs)的方法。然而,需要克服两个主要障碍,即低分析通量和缺乏商业参考材料。在这项工作中,我们展示了一种新方法,称为“单细胞同位素稀释分析”(SCIDA),用于消除这两个障碍。为了验证概念,选择巨噬细胞作为模型,在单细胞水平上研究银纳米颗粒(AgNPs)的摄取。通过微流控技术将暴露于 AgNPs 的单细胞置于阵列中;使用商业喷墨打印机,通过每个细胞都被精确分配已知皮升的浓缩同位素溶液,实现了单细胞中 AgNPs 的准确定量;通过同位素稀释 LA-ICP-MS 进行。1100 个单细胞的平均 Ag 质量为 396±219 fg Ag 细胞,与通过溶液 ICP-MS 分析确定的细胞群体的平均值一致。检测限为 0.2 fg Ag 细胞。预计 SCIDA 方法将广泛应用于单细胞水平上的细胞-NP 相互作用和 NPs 的生物学效应研究。