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Resolving drug uptake heterogeneity in 3D organ on chip models via live single-cell microsampling and ion mobility mass spectrometry
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DOI:10.1016/j.aca.2026.346065.png)
Abstract
En 中文
• An organ-on-chip platform was adapted to allow microsampling of single cells from 3D hepatocellular carcinoma models. • The extra cellular matrix effect was reduced by incorporating single-cell sample preparation and FAIMS. • Tamoxifen was successfully measured in single cells embedded in a organ-on-chip model that was exposed to a drug gradient. • The differences in drug abundance between cells correlated with their position relative to the drug channel were studied.
Journal
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6
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3.3W
Citations:
6.1W
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