Sabaté Del Río Jonathan, Son Yeonzu, Park Juhee, Sunkara Vijaya, Cho Yoon-Kyoung
Center for Algorithmic and Robotized Synthesis, Institute for Basic Science (IBS), Ulsan 44919, Republic of Korea.
Department of Biomedical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Langmuir. 2024 Dec 10;40(49):25772-25784. doi: 10.1021/acs.langmuir.4c02098. Epub 2024 Nov 28.
Extracellular vesicles (EVs) are small lipid vesicles shed by cells, carrying proteins, nucleic acids, and other molecular fingerprints. EVs have emerged as crucial mediators of cell-to-cell communication and hold great promise as biomarkers for liquid biopsies, enabling disease screening, diagnosis, prognosis, and monitoring. However, conventional EV separation methods are hampered by the presence of lipoproteins (LPs) in plasma samples, which have comparable characteristics and significantly outnumber EVs. These LPs contaminants complicate downstream analysis, compromising the accuracy of EV-based liquid biopsies. In this study, we present a lab-on-a-chip device that utilizes dielectrophoretic (DEP) separation principles to achieve efficient separation of EVs from LPs. Our method starts with a lab-on-a-disc filtration of human blood plasma gathering similar-sized EVs and LPs, followed by on-disc buffer exchange and subsequent injection into a microfluidic chip containing slanted interdigitated microelectrodes. The DEP force is negative for all EV sizes and positive for all LP sizes at 10 Hz and thus EVs are pushed away and collected at the collection outlet, whereas LPs are flowed down to the waste outlet. This two-step EVs isolation method, size-based filtration followed by DEP-based purification, offers a promising solution for enhancing the quality and accuracy of EV-based liquid biopsies.
细胞外囊泡(EVs)是细胞释放的小脂质囊泡,携带蛋白质、核酸和其他分子印记。EVs已成为细胞间通讯的关键介质,并有望成为液体活检的生物标志物,用于疾病筛查、诊断、预后和监测。然而,传统的EV分离方法受到血浆样本中脂蛋白(LPs)的影响,脂蛋白具有类似的特性且数量远多于EVs。这些LPs污染物使下游分析复杂化,影响了基于EV的液体活检的准确性。在本研究中,我们展示了一种芯片实验室设备,该设备利用介电泳(DEP)分离原理实现从LPs中高效分离EVs。我们的方法首先对人血浆进行盘上过滤,收集大小相似的EVs和LPs,然后进行盘上缓冲液交换,随后注入含有倾斜叉指微电极的微流控芯片。在10 Hz时,DEP力对所有大小的EVs为负,对所有大小的LPs为正,因此EVs被推开并在收集出口收集,而LPs则流向下游废物出口。这种两步EVs分离方法,即基于大小的过滤 followed by基于DEP的纯化,为提高基于EV的液体活检的质量和准确性提供了一个有前景的解决方案。