Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN, 46556, USA.
Electrophoresis. 2020 Nov;41(21-22):1878-1892. doi: 10.1002/elps.202000015. Epub 2020 Apr 9.
Liquid biopsy, screening cancer non-invasively and frequently by detecting and quantifying molecular markers in physiological fluids, would significantly improve cancer survival rate but it remains a distant goal. The key obstacles presented by the highly heterogeneous samples are rapid/high-yield purification and precise/selective marker capture by their antibody and oligo probes. As irregular expressions of these molecular biomarkers are the key signals, quantifying only those from the cancer cells would greatly enhance the performance of the screening tests. The recent discovery that the biomarkers are carried by nanocarriers, such as exosomes, with cell-specific membrane proteins suggests that such selection may be possible, although a new suite of fractionation and quantification technologies would need to be developed. Although under-appreciated, membrane microfluidics has made considerable contributions to resolving these issues. We review the progress made so far, based on ion-selective, track-etched, and gel membranes and advanced electrophoretic and nano-filtration designs, in this perspective and suggest future directions.
液体活检通过检测和定量生理液体中的分子标志物,无创且频繁地筛查癌症,可显著提高癌症存活率,但这仍是一个遥远的目标。高度异质样本带来的关键障碍是通过抗体和寡核苷酸探针快速/高产率地纯化和精确/选择性地捕获标志物。由于这些分子生物标志物的异常表达是关键信号,仅定量来自癌细胞的标志物将极大地提高筛选测试的性能。最近发现,生物标志物由外泌体等纳米载体携带,这些载体具有细胞特异性膜蛋白,这表明这种选择是可能的,尽管需要开发新的一系列分馏和定量技术。尽管未被充分重视,但膜微流控技术在解决这些问题方面做出了相当大的贡献。我们在这个视角下回顾了基于离子选择性、刻蚀轨迹和凝胶膜以及先进电泳和纳米过滤设计在这方面取得的进展,并提出了未来的方向。