Quantitation of amiodarone and N-desethylamiodarone in single HepG2 cells by single-cell printing-liquid vortex capture-mass spectrometry

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Abstract

Quantitative measure of a drug and its associated metabolite(s) with single-cell resolution is often limited by sampling throughput or other compromises that limit broad use. Here, we demonstrate the use of single-cell printing-liquid vortex capture-mass spectrometry (SCP-LVC-MS) to quantitatively measure the intracellular concentrations of amiodarone (AMIO) and its metabolite, N-desethylamiodarone (NDEA), from thousands of single cells across several AMIO incubation concentrations ranging from 0 to 10 μM. Concentrations obtained by SCP-LVC-MS were validated through comparison with average assays and traditional measurement of cells in bulk. Average of SCP-LVC-MS measurements and aggregate vial collection assay the concentrations differed by < 5%. Both AMIO and NDEA had clear log-normal distributions with similar standard deviation of concentrations in the cell population. The mean of both AMIO and NDEA intracellular concentrations were positively correlated with AMIO incubation concentration, increasing from 0.026 to 0.520 and 0.0055 to 0.048 mM for AMIO and NDEA, respectively. The standard deviation of AMIO and NDEA log-normal distribution fits were relatively similar in value across incubation concentrations, 0.15–0.19 log10 (mM), and exhibited a linear trend with respect to each other. The single cell-resolved conversion ratio of AMIO to NDEA increased with decreasing incubation concentration, 7 ± 2%, 18 ± 3%, and 20 ± 7% for 10.0, 1.0, and 0.1 μM AMIO incubation concentrations, respectively. Association with simultaneously measured lipids had several ions with statistically significant difference in intensity but no clear correlations with AMIO intracellular content was observed. Graphical abstract: [Figure not available: see fulltext.].

Original languageEnglish
Pages (from-to)6917-6927
Number of pages11
JournalAnalytical and Bioanalytical Chemistry
Volume413
Issue number28
DOIs
StatePublished - Nov 2021

Funding

This manuscript has been authored by UT-Battelle, LLC under Contract No. DE-AC05-00OR22725 with the US Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, and world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan ( http://energy.gov/downloads/doe-public-accesSplan ). The authors would like to thank Carmen Foster and Ann Wymore (Bioscience Division, Oak Ridge National Laboratory) for providing expertise on HepG2 cell culture and maintenance. The SCP-LVC-MS system was invented through the Laboratory Directed Research and Development Program and this work was funded through the Technology Innovation Program of Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the US Department of Energy.

FundersFunder number
Carmen Foster and Ann Wymore
U.S. Department of Energy
Oak Ridge National Laboratory

    Keywords

    • Bioanalytical methods
    • Cell systems
    • Drug monitoring
    • Drug screening
    • Single-cell analysis

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