Liquid biopsy technologies based on membrane microfluidics: High-yield purification and selective quantification of biomarkers in nanocarriers

被引:15
作者
Wang, Ceming [1 ]
Senapati, Satyajyoti [1 ]
Chang, Hsueh-Chia [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
基金
美国国家科学基金会;
关键词
cancer; extracellular vesicles; high-throughput; liquid biopsy; nanopore; EXTRACELLULAR VESICLES; PANCREATIC-CANCER; FILTRATION; EXOSOMES; FORCES; SHEAR; CHIP;
D O I
10.1002/elps.202000015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1878 / 1892
页数:15
相关论文
共 62 条
  • [1] On-Chip Immunoelectrophoresis of Extracellular Vesicles Released from Human Breast Cancer Cells
    Akagi, Takanori
    Kato, Kei
    Kobayashi, Masashi
    Kosaka, Nobuyoshi
    Ochiya, Takahiro
    Ichiki, Takanori
    [J]. PLOS ONE, 2015, 10 (04):
  • [2] Shear and AC Field Enhanced Carbon Nanotube Impedance Assay for Rapid, Sensitive, and Mismatch-Discriminating DNA Hybridization
    Basuray, Sagnik
    Senapati, Satyajyoti
    Aijian, Andrew
    Mahon, Andrew R.
    Chang, Hsueh-Chia
    [J]. ACS NANO, 2009, 3 (07) : 1823 - 1830
  • [3] Continuous micellar electrokinetic focusing of neutral species driven by ion concentration polarization
    Berzina, Beatrise
    Anand, Robbyn K.
    [J]. LAB ON A CHIP, 2019, 19 (13) : 2233 - 2240
  • [4] Mass transport across porous wall of a microtube: A facile way to diagnosis of diseased state
    Bhattacharjee, Saikat
    De, Sirshendu
    [J]. INTERNATIONAL JOURNAL OF HEAT AND MASS TRANSFER, 2018, 118 : 116 - 128
  • [5] Bonneau E, 2019, EJIFCC, V30, P114
  • [6] Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing
    Buschmann, Dominik
    Kirchner, Benedikt
    Hermann, Stefanie
    Maerte, Melanie
    Wurmser, Christine
    Brandes, Florian
    Kotschote, Stefan
    Bonin, Michael
    Steinlein, Ortrud K.
    Pfaffl, Michael W.
    Schelling, Gustav
    Reithmair, Marlene
    [J]. JOURNAL OF EXTRACELLULAR VESICLES, 2018, 7 (01)
  • [7] CAMUS MC, 1983, J LIPID RES, V24, P1210
  • [8] Chang H.-C., 2009, ELECTROKINETICALLY D
  • [9] Nanoscale Electrokinetics and Microvortices: How Microhydrodynamics Affects Nanofluidic Ion Flux
    Chang, Hsueh-Chia
    Yossifon, Gilad
    Demekhin, Evgeny A.
    [J]. ANNUAL REVIEW OF FLUID MECHANICS, VOL 44, 2012, 44 : 401 - 426
  • [10] A rapid field-use assay for mismatch number and location of hybridized DNAs
    Cheng, I-Fang
    Senapati, Satyajyoti
    Cheng, Xinguang
    Basuray, Sagnik
    Chang, Hsien-Chang
    Chang, Hsueh-Chia
    [J]. LAB ON A CHIP, 2010, 10 (07) : 828 - 831