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Rapid Isolation and Detection of Exosomes and Associated Biomarkers from Plasma

机译:从等离子体的快速分离和检测外泌体和相关生物标志物

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Exosomes found in the circulation are a primary source of important cancer-related RNA and protein biomarkers that are expected to lead to early detection, liquid biopsy, and point-of-care diagnostic applications. Unfortunately, due to their small size (50-150 nm) and low density, exosomes are extremely difficult to isolate from plasma. Current isolation methods are time-consuming multistep procedures that are unlikely to translate into diagnostic applications. To address this issue, we demonstrate the ability of an alternating current electrokinetic (ACE) microarray chip device to rapidly isolate and recover glioblastoma exosomes from undiluted human plasma samples. The ACE device requires a small plasma sample (30-50 mu L) and is able to concentrate the exosomes into high-field regions around the ACE microelectrodes within 15 min. A simple buffer wash removes bulk plasma materials, leaving the exosomes concentrated on the microelectrodes. The entire isolation process and on-chip fluorescence analysis is completed in less than 30 min which enables subsequent on-chip immunofluorescence detection of exosomal proteins, and provides viable mRNA for RT-PCR analysis. These results demonstrate the ability of the ACE device to streamline the process for isolation and recovery of exosomes, significantly reducing the number of processing steps and time required.
机译:在循环中发现的外泌体是重要的癌症相关RNA和蛋白质生物标志物的主要来源,预计会导致早期检测,液检和护理点诊断应用。遗憾的是,由于它们的小尺寸(50-150nm)和低密度,外泌体极难与等离子体隔离。当前隔离方法是耗时的多步骤,不太可能转化为诊断应用程序。为了解决这个问题,我们证明了交流电动(ACE)微阵列芯片装置快速分离和回收来自未稀释的人血浆样品的胶质母细胞瘤外泌体的能力。 ACE器件需要小的等离子体样品(30-50μm1),并且能够在15分钟内将外来物体聚集到ACE微电极周围的高场区域中。简单的缓冲洗涤清除体积等离子体材料,使浓缩在微电极上的外泌体。整个隔离过程和片上荧光分析在不到30分钟内完成,这使得随后的外源蛋白的片上免疫荧光检测,并为RT-PCR分析提供了可行的mRNA。这些结果证明了ACE器件简化了异构体分离和恢复过程的能力,显着降低了所需的处理步骤和时间的数量。

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