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Magnetic Nanoparticle-Based Microfluidic Platform for Automated Enrichment of High-Purity Extracellular Vesicles

  • Xiaoniu Guo
  • , Fei Hu
  • , Zhang Yong
  • , Shuhao Zhao
  • , Yong Wan
  • , Bingqing Wang
  • , Niancai Peng
  • Xi'an Jiaotong University
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Xi’an Key Laboratory of Biomedical Testing and High-End Equipment

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Extracellular vesicles (EVs) are available in various biological fluids and have highly heterogeneous sizes, origins, contents, and functions. Rapid enrichment of high-purity EVs remains crucial for enhancing research on EVs in tumors. In this work, we present a magnetic nanoparticle-based microfluidic platform (ExoCPR) for on-chip isolation, purification, and mild recovery of EVs from cell culture supernatant and plasma within 29 min. The ExoCPR chip integrates bubble-driven micromixers and immiscible filtration assisted by surface tension (IFAST) technology. The bubble-driven micromixer enhances the mixing between immunomagnetic beads and EVs, eliminating the need for manual pipetting or off-chip oscillatory incubation. The high-purity EVs were obtained after passing through the immiscible phase interface where hydrophilic or hydrophobic impurities nonspecifically bound to SIMI were removed. The ExoCPR chip had a capture efficiency of 75.8% and a release efficiency of 62.7% for model EVs. We also demonstrated the powerful performance of the ExoCPR in isolating EVs from biological samples (>90% purity). This chip was further employed in clinical plasma samples and showed that the number of GPC3-positive EVs isolated from hepatocellular carcinoma patients was significantly higher than that of healthy individuals. This ExoCPR chip may provide a promising tool for EV-based liquid biopsy and other fundamental research.

Original languageEnglish
Pages (from-to)7212-7219
Number of pages8
JournalAnalytical Chemistry
Volume96
Issue number18
DOIs
StatePublished - 7 May 2024

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