Department of Translational Medicine , Lund University , SE-202 13 Malmö , Sweden.
Division of Molecular Hematology and Lund Stem Cell Center , Lund University , SE-221 84 Lund , Sweden.
Anal Chem. 2018 Jul 3;90(13):8011-8019. doi: 10.1021/acs.analchem.8b00914. Epub 2018 Jun 11.
Extracellular vesicles (EVs) have emerged as a rich source of biomarkers providing diagnostic and prognostic information in diseases such as cancer. Large-scale investigations into the contents of EVs in clinical cohorts are warranted, but a major obstacle is the lack of a rapid, reproducible, efficient, and low-cost methodology to enrich EVs. Here, we demonstrate the applicability of an automated acoustic-based technique to enrich EVs, termed acoustic trapping. Using this technology, we have successfully enriched EVs from cell culture conditioned media and urine and blood plasma from healthy volunteers. The acoustically trapped samples contained EVs ranging from exosomes to microvesicles in size and contained detectable levels of intravesicular microRNAs. Importantly, this method showed high reproducibility and yielded sufficient quantities of vesicles for downstream analysis. The enrichment could be obtained from a sample volume of 300 μL or less, an equivalent to 30 min of enrichment time, depending on the sensitivity of downstream analysis. Taken together, acoustic trapping provides a rapid, automated, low-volume compatible, and robust method to enrich EVs from biofluids. Thus, it may serve as a novel tool for EV enrichment from large number of samples in a clinical setting with minimum sample preparation.
细胞外囊泡 (EVs) 已成为生物标志物的丰富来源,可提供癌症等疾病的诊断和预后信息。有必要对临床队列中 EVs 的内容进行大规模研究,但主要障碍是缺乏快速、可重复、高效且低成本的 EVs 富集方法。在这里,我们展示了一种名为声捕获的自动声基技术在富集 EVs 方面的适用性。使用这项技术,我们已经成功地从细胞培养条件培养基以及健康志愿者的尿液和血浆中富集了 EVs。声捕获的样品中含有大小从外泌体到微泡的 EVs,并含有可检测水平的囊内 microRNAs。重要的是,该方法显示出高度的重现性,并为下游分析提供了足够数量的囊泡。根据下游分析的灵敏度,可从 300 μL 或更少的样品体积中获得富集,相当于 30 分钟的富集时间。总之,声捕获提供了一种快速、自动化、低体积兼容且强大的方法,可从生物流体中富集 EVs。因此,它可能成为在临床环境中从大量样本中进行 EV 富集的新型工具,所需的样品制备量最小。