4.3 Article

Continuous CTC separation through a DEP-based contraction-expansion inertial microfluidic channel

Journal

BIOTECHNOLOGY PROGRESS
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/btpr.3341

Keywords

circulating tumor cells; contraction-expansion channel; dielectrophoresis; inertial microfluidics; label-free separation

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Efficient isolation of circulating tumor cells (CTCs) from blood is crucial for genetic analysis, cancer prediction, drug development, and treatment evaluation. Conventional methods fail to separate CTCs from white blood cells (WBCs) due to size overlap. To overcome this, a novel approach combining CE channels, DEP, and inertial microfluidics is proposed, effectively isolating CTCs from WBCs regardless of size. The method utilizes dielectric properties and size variation for label-free and continuous separation.
The efficient isolation of viable and intact circulating tumor cells (CTCs) from blood is critical for the genetic analysis of cancer cells, prediction of cancer progression, development of drugs, and evaluation of therapeutic treatments. While conventional cell separation devices utilize the size difference between CTCs and other blood cells, they fail to separate CTCs from white blood cells (WBCs) due to significant size overlap. To overcome this issue, we present a novel approach that combines curved contraction-expansion (CE) channels with dielectrophoresis (DEP) and inertial microfluidics to isolate CTCs from WBCs regardless of size overlap. This label-free and continuous separation method utilizes dielectric properties and size variation of cells for the separation of CTCs from WBCs. The results demonstrate that the proposed hybrid microfluidic channel can effectively isolate A549 CTCs from WBCs regardless of their size with a throughput of 300 mu L/min, achieving a high separation distance of 233.4 mu m at an applied voltage of 50 Vp-p. The proposed method allows for the modification of cell migration characteristics by controlling the number of CE sections of the channel, applied voltage, applied frequency, and flow rate. With its unique features of a single-stage separation, simple design, and tunability, the proposed method provides a promising alternative to the existing label-free cell separation techniques and may have a wide range of applications in biomedicine.

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