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单细胞分析:利用无标记三维质谱成像技术可视化细胞对药物和代谢物的摄取

Single-Cell Analysis: Visualizing Pharmaceutical and Metabolite Uptake in Cells with Label-Free 3D Mass Spectrometry Imaging.

作者信息

Passarelli Melissa K, Newman Carla F, Marshall Peter S, West Andrew, Gilmore Ian S, Bunch Josephine, Alexander Morgan R, Dollery Colin T

机构信息

†National Centre of Excellence in Mass Spectrometry Imaging (NiCE-MSI), National Physical Laboratory (NPL), Teddington, Middlesex, TW11 0LW, United Kingdom.

‡GlaxoSmithKline, Stevenage, United Kingdom.

出版信息

Anal Chem. 2015 Jul 7;87(13):6696-702. doi: 10.1021/acs.analchem.5b00842. Epub 2015 Jun 23.

DOI:10.1021/acs.analchem.5b00842
PMID:26023862
Abstract

Detecting metabolites and parent compound within a cell type is now a priority for pharmaceutical development. In this context, three-dimensional secondary ion mass spectrometry (SIMS) imaging was used to investigate the cellular uptake of the antiarrhythmic agent amiodarone, a phospholipidosis-inducing pharmaceutical compound. The high lateral resolution and 3D imaging capabilities of SIMS combined with the multiplex capabilities of ToF mass spectrometric detection allows for the visualization of pharmaceutical compound and metabolites in single cells. The intact, unlabeled drug compound was successfully detected at therapeutic dosages in macrophages (cell line: NR8383). Chemical information from endogenous biomolecules was used to correlate drug distributions with morphological features. From this spatial analysis, amiodarone was detected throughout the cell, with the majority of the compound found in the membrane and subsurface regions and absent in the nuclear regions. Similar results were obtained when the macrophages were doped with amiodarone metabolite, desethylamiodarone. The fwhm lateral resolution measured across an intracellular interface in high lateral resolution ion images was approximately 550 nm. Overall, this approach provides the basis for studying cellular uptake of pharmaceutical compounds and their metabolites on the single cell level.

摘要

在细胞类型中检测代谢物和母体化合物是目前药物研发的重点。在此背景下,三维二次离子质谱(SIMS)成像被用于研究抗心律失常药物胺碘酮(一种可诱导磷脂沉积症的药物化合物)的细胞摄取情况。SIMS的高横向分辨率和三维成像能力与飞行时间质谱检测的多重能力相结合,使得在单细胞中可视化药物化合物及其代谢物成为可能。在巨噬细胞(细胞系:NR8383)中,以治疗剂量成功检测到完整的、未标记的药物化合物。利用内源性生物分子的化学信息将药物分布与形态特征相关联。通过这种空间分析,在整个细胞中都检测到了胺碘酮,大部分化合物存在于细胞膜和亚表面区域,而核区域则没有。当巨噬细胞掺入胺碘酮代谢物去乙基胺碘酮时,也得到了类似的结果。在高横向分辨率离子图像中跨细胞内界面测量的半高宽横向分辨率约为550纳米。总体而言,这种方法为在单细胞水平上研究药物化合物及其代谢物的细胞摄取提供了基础。

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