Microfluidic-Assisted CTC Isolation and In Situ Monitoring Using Smart Magnetic Microgels

Small. 2023 Apr;19(16):e2205320. doi: 10.1002/smll.202205320. Epub 2023 Jan 31.

Abstract

Capturing rare disease-associated biomarkers from body fluids can offer an early-stage diagnosis of different cancers. Circulating tumor cells (CTCs) are one of the major cancer biomarkers that provide insightful information about the cancer metastasis prognosis and disease progression. The most common clinical solutions for quantifying CTCs rely on the immunomagnetic separation of cells in whole blood. Microfluidic systems that perform magnetic particle separation have reported promising outcomes in this context, however, most of them suffer from limited efficiency due to the low magnetic force generated which is insufficient to trap cells in a defined position within microchannels. In this work, a novel method for making soft micromagnet patterns with optimized geometry and magnetic material is introduced. This technology is integrated into a bilayer microfluidic chip to localize an external magnetic field, consequently enhancing the capture efficiency (CE) of cancer cells labeled with the magnetic nano/hybrid microgels that are developed in the previous work. A combined numerical-experimental strategy is implemented to design the microfluidic device and optimize the capturing efficiency and to maximize the throughput. The proposed design enables high CE and purity of target cells and real-time time on-chip monitoring of their behavior. The strategy introduced in this paper offers a simple and low-cost yet robust opportunity for early-stage diagnosis and monitoring of cancer-associated biomarkers.

Keywords: bilayer microfluidic chips; cell isolation; micromagnets; nano/hybrid microgels; thermoresponsive.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Separation / methods
  • Humans
  • Immunomagnetic Separation / methods
  • Magnetic Phenomena
  • Microfluidic Analytical Techniques* / methods
  • Microfluidics
  • Microgels*
  • Neoplastic Cells, Circulating* / pathology

Substances

  • Microgels