posted on 2025-02-27, 20:36authored byXudong Zhao, Xiang Liu, Tucan Chen, Han Xie, Shunji Li, Ying Zhang, Hongwei Zhang, Yulin Cao, Wei Du, Xiaojun Feng, Xin Liu, Yiwei Li, Peng Chen, Qiubai Li, Bi-Feng Liu
Exosomes present in the circulatory system demonstrate
considerable
promise for the diagnosis and treatment of diseases. Nevertheless,
the complex nature of blood samples and the prevalence of highly abundant
proteins pose a significant obstacle to prompt and effective isolation
and functional evaluation of exosomes from blood. Here, we present
a fully integrated lab-on-a-disc equipped with two nanofilters, also
termed iExoDisc, which facilitates automated isolation of exosomes
from 400 μL blood samples within 45 min. By integrating the
plasma separation module, highly abundant protein removal module,
and nanopore membrane-based total isolation module, the resulting
exosomes exhibited significantly increased purity (∼3–6-fold)
compared to conventional ultracentrifugation and polymer precipitation.
Additionally, we then successfully performed nontargeted and targeted
glycan profiling on exosomes derived from clinical triple-negative
breast cancer (TNBC) patients using MALDI-TOF-MS and lectin microarray
containing 56 kinds of lectins. The findings from both methodologies
indicated that galactosylation and sialylation exhibit potential as
diagnostic indicators for TNBC. Finally, by utilizing the exosome-specific
glycosylated protein CD63 as a proof-of-concept, we successfully realized
the integration of point-of-care on-chip exosome separation and in
situ detection with 2 h. Thus, the iExoDisc provides a potential approach
to early cancer detection, liquid biopsy, and point-of-care diagnosis.