外体
微泡
化学
液体活检
限制
分离(微生物学)
纳米粒子跟踪分析
流式细胞术
污渍
小泡
细胞生物学
细胞外小泡
免疫印迹
生物物理学
纳米颗粒
泌尿系统
色谱法
细胞培养
分子生物学
RNA提取
生物
纳米技术
生物流体
作者
Taewoon Kim,Wonseok Kim,Sung-Jae Kim,Luke P. Lee,Jong Wook Hong
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-11-10
标识
DOI:10.1021/acs.nanolett.5c04885
摘要
Urine-based liquid biopsy and exosomes constitute exceptional noninvasive techniques for detecting valuable biomarkers associated with diverse diseases. However, current exosome isolation methods struggle to recover sufficient intact exosomes from a large volume of diluted urine, limiting high detection sensitivity. Here, we present a highly sensitive method for detecting exosome markers using microfluidics-based biologically intact exosome separation technology (BEST), which isolates and enriches exosomes from human urine. Numerical simulations demonstrate that hydrodynamic wall repulsion and suction-driven drag forces segregate 100 nm particles representing exosomes from 8 μm particles, indicating apoptotic bodies or larger particles with complete purity, consistent with experiments. We also show a separation purity of 72.4% for urinary exosomes at a suction flow rate of 95 μL/min. Using concentrated exosomes, PCR and Western blotting sensitivities increase by 4.7 and 4.0-fold, respectively, compared with unprocessed pooled urine. Our methodology possesses considerable potential for future molecular diagnostics, necessitating heightened sensitivity.
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