Bathini Srinivas, Pakkiriswami Shanmugasundaram, Ouellette Rodney J, Ghosh Anirban, Packirisamy Muthukumaran
Optical Bio-Microsystems Laboratory, Department of Mechanical Engineering, Concordia University, Montreal, Canada.
Department of Biochemistry and Molecular Biology, Dalhousie Medicine New Brunswick, Saint John, New Brunswick, Canada.
Biosens Bioelectron. 2021 Dec 15;194:113585. doi: 10.1016/j.bios.2021.113585. Epub 2021 Aug 27.
Extracellular vesicles (EVs) are the cell-derived vesicles which play a critical role in cell-to-cell communication, and disease progression. These vesicles contain a myriad of substances like RNA, DNA, proteins, and lipids from their origin cells, offering a good source of biomarkers. The existing methods for the isolation of EVs are time-consuming, lack yield and purity, and expensive. In this work, we present a magnetic particle based liquid biopsy chip for the isolation of EVs by using a synthetic peptide, Vn96. To ensure capture efficiency, a 3D mixer is integrated in the chip, along with a sedimentation unit, which allows EV-captured magnetic particles to settle in it based on gravity assisted sedimentation. The captured EVs are then isolated for their elution and validation. The EVs are characterized by the scanning electron microscopy (SEM) measurements and the ability of capture and isolation of EVs is validated by the nanoparticle tracking analysis (NTA) and atomic force microscopy (AFM). The DNA content of the EVs is further characterized by the absolute quantification of a housekeeping gene (RNase P) copies using droplet digital PCR (ddPCR). The results show that the chip can capture and isolate the EVs, without affecting their morphology. Thus, the liquid biopsy chip can be considered as a potential point of care device for diagnostics in a clinical setting.
细胞外囊泡(EVs)是细胞衍生的囊泡,在细胞间通讯和疾病进展中起关键作用。这些囊泡包含来自其起源细胞的大量物质,如RNA、DNA、蛋白质和脂质,是生物标志物的良好来源。现有的EVs分离方法耗时、产量和纯度低且昂贵。在这项工作中,我们展示了一种基于磁性颗粒的液体活检芯片,用于通过使用合成肽Vn96分离EVs。为确保捕获效率,芯片中集成了一个3D混合器以及一个沉降单元,该沉降单元允许捕获了EVs的磁性颗粒基于重力辅助沉降在其中沉降。然后将捕获的EVs分离出来进行洗脱和验证。通过扫描电子显微镜(SEM)测量对EVs进行表征,并通过纳米颗粒跟踪分析(NTA)和原子力显微镜(AFM)验证EVs的捕获和分离能力。使用液滴数字PCR(ddPCR)对管家基因(RNase P)拷贝进行绝对定量,进一步表征EVs的DNA含量。结果表明,该芯片可以捕获和分离EVs,而不影响其形态。因此,该液体活检芯片可被视为临床环境中诊断的潜在即时护理设备。