Intracellular Drug Uptake A Comparison of Single Cell Measurements Using ToF-SIMS Imaging and Quantification from Cell Populations with LC/MS/MS

被引:30
作者
Newman, Carla F. [1 ,3 ]
Havelund, Rasmus [2 ]
Passarelli, Melissa K. [2 ]
Marshall, Peter S. [1 ]
Francis, Ian [1 ]
West, Andy [1 ]
Alexander, Morgan R. [3 ]
Gilmore, Ian S. [2 ]
Dollery, Colin T. [1 ]
机构
[1] GlaxoSmithKline, Stevenage SG1 2NY, Herts, England
[2] Natl Ctr Excellence Mass Spectrometry Imaging NiC, NPL, Teddington TW11 0LW, Middx, England
[3] Univ Nottingham, Sch Pharm, Div Adv Mat & Healthcare Technol, Univ Pk, Nottingham NG7 2RD, England
关键词
ION MASS-SPECTROMETRY; LYSOSOMAL SEQUESTRATION; ALVEOLAR MACROPHAGES; RESPIRATORY DRUGS; DISCOVERY; ACCUMULATION; PERMEABILITY; AMIODARONE; CHALLENGES; EFFICIENCY;
D O I
10.1021/acs.analchem.7b01436
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
ToF-SIMS is a label-free imaging method that has been shown to enable imaging of amiodarone in single rat macrophage (NR8383) cells. In this study, we show that the method extends to three other cell lines relevant to drug discovery: human embryonic kidney (HEK293), cervical cancer (HeLa), and liver cancer (HepG2). There is significant interest in the variation of drug uptake at the single cell level, and we use ToF-SIMS to show that there is great diversity between individual cells and when comparing each of the cell types. These single cell measurements are compared to quantitative measurements of cell-associated amiodarone for the population using LC/MS/MS and cell counting with flow cytometry. NR8383 and HepG2 cells uptake the greatest amount of amiodarone with an average of 2.38 and 2.60 pg per cell, respectively, and HeLa and Hek 293 have a significantly lower amount of amiodarone at 0.43 and 0.36 pg per cell, respectively. The amount of cell-associated drug for the ensemble population measurement (LC/MS/MS) is compared with the ToF-SIMS single cell data: a similar amount of drug was detected per cell for the NR8383, and HepG2 cells at a greater level than that for the HEK293 cells. However, the two techniques did not agree for the HeLa cells, and we postulate potential reasons for this.
引用
收藏
页码:11944 / 11953
页数:10
相关论文
共 49 条
  • [1] The role of negatively charged lipids in lysosomal phospholipase A2 function
    Abe, Akira
    Shayman, James A.
    [J]. JOURNAL OF LIPID RESEARCH, 2009, 50 (10) : 2027 - 2035
  • [2] Acton QA, 2013, ISSUES BIOMEDICAL EN
  • [3] Single-cell biology
    不详
    [J]. NATURE, 2017, 547 (7661) : 19 - 19
  • [4] [Anonymous], 2014, ASSAY GUIDANCE MANUA
  • [5] ACCUMULATION OF AMIODARONE AND DESETHYLAMIODARONE BY RAT ALVEOLAR MACROPHAGES IN CELL-CULTURE
    ANTONINI, JM
    REASOR, MJ
    [J]. BIOCHEMICAL PHARMACOLOGY, 1991, 42 : S151 - S156
  • [6] The properties of known drugs .1. Molecular frameworks
    Bemis, GW
    Murcko, MA
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (15) : 2887 - 2893
  • [7] Argon Cluster Ion Source Evaluation on Lipid Standards and Rat Brain Tissue Samples
    Bich, Claudia
    Havelund, Rasmus
    Moellers, Rudolf
    Touboul, David
    Kollmer, Felix
    Niehuis, Ewald
    Gilmore, Ian S.
    Brunelle, Alain
    [J]. ANALYTICAL CHEMISTRY, 2013, 85 (16) : 7745 - 7752
  • [8] Biological tissue imaging with time-of-flight secondary ion mass spectrometry and cluster ion sources
    Brunelle, A
    Touboul, D
    Laprévote, O
    [J]. JOURNAL OF MASS SPECTROMETRY, 2005, 40 (08): : 985 - 999
  • [9] STED microscopy for nanoscale imaging in living brain slices
    Chereau, Ronan
    Tonnesen, Jan
    Naegerl, U. Valentin
    [J]. METHODS, 2015, 88 : 57 - 66
  • [10] Intracellular Drug Concentrations
    Dollery, C. T.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2013, 93 (03) : 263 - 266