Department of Health Technology, Technical University of Denmark, Oersteds Plads building 345c, 2800, Kongens Lyngby, Denmark.
Nat Commun. 2020 May 11;11(1):2337. doi: 10.1038/s41467-020-15889-3.
Exosomes are nanometer-sized lipid vesicles present in liquid biopsies and used as biomarkers for several diseases including cancer, Alzheimer's, and central nervous system diseases. Purification and subsequent size and surface characterization are essential to exosome-based diagnostics. Sample purification is, however, time consuming and potentially damaging, and no current method gives the size and zeta potential from a single measurement. Here, we concentrate exosomes from a dilute solution and measure their size and zeta potential in a one-step measurement with a salt gradient in a capillary channel. The salt gradient causes oppositely directed particle and fluid transport that trap particles. Within minutes, the particle concentration increases more than two orders of magnitude. A fit to the spatial distribution of a single or an ensemble of exosomes returns both their size and surface charge. Our method is applicable for other types of nanoparticles. The capillary is fabricated in a low-cost polymer device.
外泌体是存在于液体活检中的纳米级脂质囊泡,可作为包括癌症、阿尔茨海默病和中枢神经系统疾病在内的多种疾病的生物标志物。外泌体的分离和后续的大小及表面特征分析对于基于外泌体的诊断至关重要。然而,样品分离既费时又可能造成损伤,而且目前没有哪种方法可以在单次测量中提供大小和 zeta 电位。在此,我们从稀释溶液中浓缩外泌体,并在毛细管通道中的盐梯度中进行一步测量,测量其大小和 zeta 电位。盐梯度会导致粒子和流体的反向运输,从而捕获粒子。在数分钟内,粒子浓度增加两个数量级以上。对单个或多个外泌体的空间分布进行拟合,可以同时得到它们的大小和表面电荷。我们的方法适用于其他类型的纳米颗粒。该毛细管由低成本聚合物器件制造。