An FDA-Validated, Self-Cleaning Liquid Chromatography-Mass Spectrometry System for Determining Small-Molecule Drugs and Metabolites in Organoid/Organ-on-Chip Medium.
Stian KoglerGustav Mathingsdal PedersenFelipe Martínez-RamírezAleksandra AizenshtadtMathias BusekStefan J K KraussSteven Ray WilsonHanne Røberg-LarsenPublished in: Analytical chemistry (2024)
As organoids and organ-on-chip (OoC) systems move toward preclinical and clinical applications, there is an increased need for method validation. Using a liquid chromatography-mass spectrometry (LC-MS)-based approach, we developed a method for measuring small-molecule drugs and metabolites in the cell medium directly sampled from liver organoids/OoC systems. The LC-MS setup was coupled to an automatic filtration and filter flush system with online solid-phase extraction (SPE), allowing for robust and automated sample cleanup/analysis. For the matrix, rich in, e.g., protein, salts, and amino acids, no preinjection sample preparation steps (protein precipitation, SPE, etc.) were necessary. The approach was demonstrated with tolbutamide and its liver metabolite, 4-hydroxytolbutamide (4HT). The method was validated for analysis of cell media of human stem cell-derived liver organoids cultured in static conditions and on a microfluidic platform according to Food and Drug Administration (FDA) guidelines with regards to selectivity, matrix effects, accuracy, precision, etc. The system allows for hundreds of injections without replacing chromatography hardware. In summary, drug/metabolite analysis of organoids/OoCs can be performed robustly with minimal sample preparation.
Keyphrases
- liquid chromatography
- solid phase extraction
- mass spectrometry
- molecularly imprinted
- small molecule
- tandem mass spectrometry
- high throughput
- high performance liquid chromatography
- high resolution mass spectrometry
- liquid chromatography tandem mass spectrometry
- ultra high performance liquid chromatography
- single cell
- induced pluripotent stem cells
- simultaneous determination
- gas chromatography
- ms ms
- protein protein
- gas chromatography mass spectrometry
- cell therapy
- endothelial cells
- amino acid
- drug administration
- circulating tumor cells
- high resolution
- machine learning
- capillary electrophoresis
- deep learning
- healthcare
- social media
- drug induced
- clinical practice
- binding protein
- risk assessment
- emergency department
- ionic liquid