4.8 Review

Microfluidic-Based Exosome Analysis for Liquid Biopsy

期刊

SMALL METHODS
卷 5, 期 3, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202001131

关键词

exosomes detection; exosomes isolation; liquid biopsy; microfluidic chips

资金

  1. National Natural Science Foundation of China [21735004, 21874089, 21927806, 22004084]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT13036]
  3. Innovative Research Team of High-level Local Universities in Shanghai
  4. National Key R&D Program of China [2019YFA0905800]

向作者/读者索取更多资源

Liquid biopsy based on exosomes provides valuable information for biomarker analysis, but faces challenges in exosome isolation and molecular detection. The advancement of microfluidics technology has significantly improved the selectivity and sensitivity of exosome capture and molecular detection.
Liquid biopsy offers non-invasive and real-time molecular profiling of individual patients, and is thus considered a revolutionary technology in precision medicine. Exosomes have been acknowledged as significant biomarkers in liquid biopsy, as they play a central role in cell-cell communication and are closely related to the pathogenesis of most human malignancies. Nevertheless, in biofluids exosomes always co-exist with other particles, and the cargo components of exosomes are highly heterogeneous. Thus, the isolation and molecular characterization of exosomes are still technically challenging. Microfluidics technology effectively addresses this challenge by virtue of its inherent advantages, such as precise manipulation of fluids, low consumption of samples and reagents, and a high level of integration. Recent advances in microfluidics allow in situ exosome capture and molecular detection with unprecedented selectivity and sensitivity. In this review, the state-of-the-art developments in microfluidics-based exosome research, including exosome isolation approaches and molecular detection strategies, with highlights of the characterization of exosomal biomarkers in cancer liquid biopsy is summarized. The major challenges are also discussed and some perspectives for the future directions of exosome-based liquid biopsy in microfluidic systems are presented.

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