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Isolation of Extracellular Vesicles from Biological Fluids via the Aggregation–Precipitation Approach for Downstream miRNAs Detection

机译:通过对下游MiRNA检测的聚集沉淀方法分离生物流体的细胞外囊囊泡

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摘要

Extracellular vesicles (EVs) have high potential as sources of biomarkers for non-invasive diagnostics. Thus, a simple and productive method of EV isolation is demanded for certain scientific and medical applications of EVs. Here we aim to develop a simple and effective method of EV isolation from different biofluids, suitable for both scientific, and clinical analyses of miRNAs transported by EVs. The proposed aggregation–precipitation method is based on the aggregation of EVs using dextran blue and the subsequent precipitation of EVs using 1.5% polyethylene glycol solutions. The developed method allows the effective isolation of EVs from plasma and urine. As shown using TEM, dynamic light scattering, and miRNA analyses, this method is not inferior to ultracentrifugation-based EV isolation in terms of its efficacy, lack of inhibitors for polymerase reactions and applicable for both healthy donors and cancer patients. This method is fast, simple, does not need complicated equipment, can be adapted for different biofluids, and has a low cost. The aggregation–precipitation method of EV isolation accessible and suitable for both research and clinical laboratories. This method has the potential to increase the diagnostic and prognostic utilization of EVs and miRNA-based diagnostics of urogenital pathologies.
机译:细胞外囊泡(EVS)具有高潜力作为非侵入性诊断的生物标志物来源。因此,对于EVS的某些科学和医学应用,需要一种简单且生产的EV隔离方法。在这里,我们的目标是从不同的生物流体开发一种简单有效的EV隔离方法,适用于EVS运输的MiRNA的科学和临床分析。所提出的聚集沉淀方法基于使用葡聚糖蓝的EVS的聚集以及使用1.5%聚乙二醇溶液的EVS的随后沉淀。开发的方法允许从血浆和尿液中有效地分离EV。如图所示,使用TEM,动态光散射和miRNA分析,该方法在其功效方面不差不等,缺乏聚合酶反应的抑制剂和适用于健康供体和癌症患者的抑制剂。这种方法快速,简单,不需要复杂的设备,可以适用于不同的生物流体,并且具有低成本。 EV隔离的聚集沉淀方法可接近,适用于研究和临床实验室。该方法有可能提高促进病理学的EVS和MiRNA的诊断和预后利用。

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