Microfluidic-SERS technologies for CTC: a perspective on clinical translation

Amin Hassanzadeh-Barforoushi, Anastasiia Tukova, Audrey Nadalini, David W. Inglis, Simon Chang-Hao Tsao*, Yuling Wang*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

11 Citations (Scopus)

Abstract

Enumeration and phenotypic profiling of circulating tumor cells (CTCs) provide critical information for clinical diagnosis and treatment monitoring in cancer. To achieve this goal, an integrated system is needed to efficiently isolate CTCs from patient samples and sensitively evaluate their phenotypes. Such integration would comprise a high-throughput single-cell processing unit for the isolation and manipulation of CTCs and a sensitive and multiplexed quantitation unit to detect clinically relevant signals from these cells. Surface-enhanced Raman scattering (SERS) has been used as an analytical method for molecular profiling and in vitro cancer diagnosis. More recently, its multiplexing capability and power to create distinct molecular signatures against their targets have garnered attention. Here, we share our insights into the combined power of microfluidics and SERS in realizing CTC isolation, enumeration, and detection from a clinical translation perspective. We highlight the key operational factors in CTC microfluidic processing and SERS detection from patient samples. We further discuss microfluidic-SERS integration and its clinical utility as a paradigm shift in clinical CTC-based cancer diagnosis and prognostication. Finally, we summarize the challenges and attempt to look forward to what lies ahead of us in potentially translating the technique into real clinical applications.

Original languageEnglish
Pages (from-to)22761-22775
Number of pages15
JournalACS Applied Materials and Interfaces
Volume16
Issue number18
Early online date23 Apr 2024
DOIs
Publication statusPublished - 8 May 2024

Keywords

  • Cancer
  • cancer detection
  • circulating tumor cells
  • epithelial-to-mesenchymal transition
  • metastasis
  • microfluidics
  • surface-enhanced Raman scattering

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