微泡
外体
免疫分析
检出限
癌症
化学
纳米技术
材料科学
癌症生物标志物
癌细胞
微流控
纳米粒子跟踪分析
色谱法
医学
小RNA
生物化学
抗体
免疫学
内科学
基因
作者
Chunchen Liu,Xiaonan Xu,Bo Li,Bo Situ,Weilun Pan,Yu Hu,Taixue An,Shuhuai Yao,Lei Zheng
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-06-11
卷期号:18 (7): 4226-4232
被引量:330
标识
DOI:10.1021/acs.nanolett.8b01184
摘要
Exosomes shed by tumor cells have been recognized as promising biomarkers for cancer diagnostics due to their unique composition and functions. Quantification of low concentrations of specific exosomes present in very small volumes of clinical samples may be used for noninvasive cancer diagnosis and prognosis. We developed an immunosorbent assay for digital qualification of target exosomes using droplet microfluidics. The exosomes were immobilized on magnetic microbeads through sandwich ELISA complexes tagged with an enzymatic reporter that produces a fluorescent signal. The constructed beads were further isolated and encapsulated into a sufficient number of droplets to ensure only a single bead was encapsulated in a droplet. Our droplet-based single-exosome-counting enzyme-linked immunoassay (droplet digital ExoELISA) approach enables absolute counting of cancer-specific exosomes to achieve unprecedented accuracy. We were able to achieve a limit of detection (LOD) down to 10 enzyme-labeled exosome complexes per microliter (∼10–17 M). We demonstrated the application of the droplet digital ExoELISA platform in quantitative detection of exosomes in plasma samples directly from breast cancer patients. We believe our approach may have the potential for early diagnosis of cancer and accelerate the discovery of cancer exosomal biomarkers for clinical diagnosis.
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