Cascaded elasto-inertial separation of malignant tumor cells from untreated malignant pleural and peritoneal effusions.
Chen NiDan WuYao ChenSilin WangNan XiangPublished in: Lab on a chip (2024)
Separation of malignant tumor cells (MTCs) from large background cells in untreated malignant pleural and peritoneal effusions (MPPEs) is critical for improving the sensitivity and efficiency of cytological diagnosis. Herein, we proposed a cascaded elasto-inertial cell separation (CEICS) device integrating an interfacial elasto-inertial microfluidic channel with a symmetric contraction expansion array (CEA) channel for pretreatment-free, high-recovery-ratio, and high-purity separation of MTCs from clinical MPPEs. First, the effects of flow-rate ratio, cell concentration, and cell size on separation performances in two single-stage channels were investigated. Then, the performances of the integrated CEICS device were characterized using blood cells spiked with three different tumor cells (MCF-7, MDA-MB-231, and A549 cells) at a high total throughput of 240 μL min -1 . An average recovery ratio of ∼95% and an average purity of ∼61% for the three tumor cells were achieved. Finally, we successfully applied the CEICS device for the pretreatment-free separation of MTCs from clinical MPPEs of different cancers. Our CEICS device may provide a preparation tool for improving the sensitivity and efficiency of cytological examination.
Keyphrases
- induced apoptosis
- cell cycle arrest
- liquid chromatography
- single cell
- stem cells
- endoplasmic reticulum stress
- high throughput
- mass spectrometry
- oxidative stress
- signaling pathway
- circulating tumor cells
- mesenchymal stem cells
- molecular dynamics simulations
- pi k akt
- bone marrow
- tandem mass spectrometry
- atomic force microscopy
- electron transfer