Fast and Label-Free Isolation of Circulating Tumor Cells from Blood: From a Research Microfluidic Platform to an Automated Fluidic Instrument, VTX-1 Liquid Biopsy System

SLAS Technol. 2018 Feb;23(1):16-29. doi: 10.1177/2472630317738698.

Abstract

Tumor tissue biopsies are invasive, costly, and collect a limited cell population not completely reflective of patient cancer cell diversity. Circulating tumor cells (CTCs) can be isolated from a simple blood draw and may be representative of the diverse biology from multiple tumor sites. The VTX-1 Liquid Biopsy System was designed to automate the isolation of clinically relevant CTC populations, making the CTCs available for easy analysis. We present here the transition from a cutting-edge microfluidic innovation in the lab to a commercial, automated system for isolating CTCs directly from whole blood. As the technology evolved into a commercial system, flexible polydimethylsiloxane microfluidic chips were replaced by rigid poly(methyl methacrylate) chips for a 2.2-fold increase in cell recovery. Automating the fluidic processing with the VTX-1 further improved cancer cell recovery by nearly 1.4-fold, with a 2.8-fold decrease in contaminating white blood cells and overall improved reproducibility. Two isolation protocols were optimized that favor either the cancer cell recovery (up to 71.6% recovery) or sample purity (≤100 white blood cells/mL). The VTX-1's performance was further tested with three different spiked breast or lung cancer cell lines, with 69.0% to 79.5% cell recovery. Finally, several cancer research applications are presented using the commercial VTX-1 system.

Keywords: VTX-1 Liquid Biopsy System; circulating tumor cells (CTCs); liquid biopsy; poly(methyl methacrylate) (PMMA) microfluidic chips; polydimethylsiloxane (PDMS) deformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Automation, Laboratory / instrumentation
  • Automation, Laboratory / methods*
  • Blood Cells*
  • Cell Separation / instrumentation
  • Cell Separation / methods*
  • Humans
  • Liquid Biopsy / instrumentation
  • Liquid Biopsy / methods*
  • Microfluidics / instrumentation
  • Microfluidics / methods*
  • Neoplastic Cells, Circulating*
  • Reproducibility of Results