Microsystem Technologies

, Volume 20, Issue 10, pp 1815–1825

Arrays of high-aspect ratio microchannels for high-throughput isolation of circulating tumor cells (CTCs)

Authors

    • Department of Biomedical EngineeringUniversity of North Carolina
    • BioFluidica, Inc.
  • Joshua M. Jackson
    • Department of ChemistryUniversity of North Carolina
  • Hong Wang
    • Department of Biomedical EngineeringUniversity of North Carolina
  • Małgorzata A. Witek
    • Department of Biomedical EngineeringUniversity of North Carolina
  • Joyce Kamande
    • Department of ChemistryLouisiana State University
  • Matthew I. Milowsky
    • Lineberger Comprehensive Cancer CenterUNC School of Medicine
  • Young E. Whang
    • Lineberger Comprehensive Cancer CenterUNC School of Medicine
    • Department of Biomedical EngineeringUniversity of North Carolina
    • Department of ChemistryUniversity of North Carolina
    • Lineberger Comprehensive Cancer CenterUNC School of Medicine
    • BioFluidica, Inc.
Technical Paper

DOI: 10.1007/s00542-013-1941-6

Cite this article as:
Hupert, M.L., Jackson, J.M., Wang, H. et al. Microsyst Technol (2014) 20: 1815. doi:10.1007/s00542-013-1941-6

Abstract

Microsystem-based technologies are providing new opportunities in the area of in vitro diagnostics due to their ability to provide process automation enabling point-of-care operation. As an example, microsystems used for the isolation and analysis of circulating tumor cells (CTCs) from complex, heterogeneous samples in an automated fashion with improved recoveries and selectivity are providing new opportunities for this important biomarker. Unfortunately, many of the existing microfluidic systems lack the throughput capabilities and/or are too expensive to manufacture to warrant their widespread use in clinical testing scenarios. Here, we describe a disposable, all-polymer, microfluidic system for the high-throughput (HT) isolation of CTCs directly from whole blood inputs. The device employs an array of high aspect ratio (HAR), parallel, sinusoidal microchannels (25 × 150 μm; W × D; AR = 6.0) with walls covalently decorated with anti-EpCAM antibodies to provide affinity-based isolation of CTCs. Channel width, which is similar to an average CTC diameter (10–20 μm), plays a critical role in maximizing the probability of cell/wall interactions and allows for achieving high CTC recovery. The extended channel depth allows for increased throughput at the optimized flow velocity (2 mm/s in a microchannel); maximizes cell recovery, and prevents clogging of the microfluidic channels during blood processing. Fluidic addressing of the microchannel array with a minimal device footprint is provided by large cross-sectional area feed and exit channels poised orthogonal to the network of the sinusoidal capillary channels (so-called Z-geometry). Computational modeling was used to confirm uniform addressing of the channels in the isolation bed. Devices with various numbers of parallel microchannels ranging from 50 to 320 have been successfully constructed. Cyclic olefin copolymer (COC) was chosen as the substrate material due to its superior properties during UV-activation of the HAR microchannels surfaces prior to antibody attachment. Operation of the HT-CTC device has been validated by isolation of CTCs directly from blood secured from patients with metastatic prostate cancer. High CTC sample purities (low number of contaminating white blood cells) allowed for direct lysis and molecular profiling of isolated CTCs.

Copyright information

© Springer-Verlag Berlin Heidelberg 2013