Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads.
Seung Joon LeeTae Seok SimHyun Young ShinJungmin LeeMin Young KimJoseph SunooJeong-Gun LeeKyungmoo YeaYoung Zoon KimDanny van NoortSoo Kyung ParkWoon-Hae KimKyun Woo ParkMinseok S KimPublished in: PloS one (2019)
Microchips are widely used to separate circulating tumor cells (CTCs) from whole blood by virtues of sophisticated manipulation for microparticles. Here, we present a chip with an 8 μm high and 27.9 mm wide slit to capture cancer cells bound to 3 μm beads. Apart from a higher purity and recovery rate, the slit design allows for simplified fabrication, easy cell imaging, less clogging, lower chamber pressure and, therefore, higher throughput. The beads were conjugated with anti-epithelial cell adhesion molecules (anti-EpCAM) to selectively bind to breast cancer cells (MCF-7) used to spike the whole blood. The diameter of the cell-bead construct was in average 23.1 μm, making them separable from other cells in the blood. As a result, the cancer cells were separated from 5 mL of whole blood with a purity of 52.0% and a recovery rate of 91.1%, and also we confirmed that the device can be applicable to clinical samples of human breast cancer patients. The simple design with microslit, by eliminating any high-aspect ratio features, is expected to reduce possible defects on the chip and, therefore, more suitable for mass production without false separation outputs.
Keyphrases
- circulating tumor cells
- breast cancer cells
- cell adhesion
- circulating tumor
- single cell
- cell therapy
- induced apoptosis
- endothelial cells
- high resolution
- stem cells
- cell cycle arrest
- photodynamic therapy
- oxidative stress
- signaling pathway
- bone marrow
- endoplasmic reticulum stress
- induced pluripotent stem cells
- fluorescence imaging