TY - JOUR
T1 - Micro- And Nanopillar Chips for Continuous Separation of Extracellular Vesicles
AU - Hattori, Yuya
AU - Shimada, Taisuke
AU - Yasui, Takao
AU - Kaji, Noritada
AU - Baba, Yoshinobu
N1 - Funding Information:
This work was partially supported by JST/PRESTO (Grant Nos. JPMJPR16F4, JPMJPR151B), Grant-in-Aid for Scientific Research on Innovative Areas (18H04545), Nanotechnology Platform Program (Molecule and Material Synthesis) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), a JSPS Grant-in-Aid for Scientific Research (A) [16H02091], the ImPACT Program of the Council for Science, Technology and Innovation (Cabinet Office, Government of Japan), and a research grant from the Nitto Foundation.
Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/5/21
Y1 - 2019/5/21
N2 - Micro- and nanopillar chips are widely used to separate and enrich biomolecules, such as DNA, RNA, protein, and cells, as an analytical technique and to provide a confined nanospace for polymer science analyses. Herein, we demonstrated a continuous accurate and precise separation technique for extracellular vesicles (EVs), nanometer-sized vesicles (typically 50-200 nm) currently recognized as novel biomarkers present in biofluids, based on the principle of electroosmotic flow-driven deterministic lateral displacement in micro- and nanopillar array chips. Notably, the easy-to-operate flow control afforded by electroosmotic flow allowed nanoparticles 50-500 nm in size, including EVs, to be precisely separated and enriched in a continuous manner. By observation of the flow behavior of nanoparticles, we found that electroosmotic flow velocity in the nanopillar arrays did not solely depend on counterion mobility on the surface of nanopillar chips, but rather showed a parabolic flow profile. This hydrodynamic pressure-free and easy-to-use separation and enrichment technique, which requires only electrode insertion into the reservoirs and electric field application, may thus serve as a promising technique for future precise and accurate EV analysis, reflecting both size and composition for research and potential clinical diagnostic applications.
AB - Micro- and nanopillar chips are widely used to separate and enrich biomolecules, such as DNA, RNA, protein, and cells, as an analytical technique and to provide a confined nanospace for polymer science analyses. Herein, we demonstrated a continuous accurate and precise separation technique for extracellular vesicles (EVs), nanometer-sized vesicles (typically 50-200 nm) currently recognized as novel biomarkers present in biofluids, based on the principle of electroosmotic flow-driven deterministic lateral displacement in micro- and nanopillar array chips. Notably, the easy-to-operate flow control afforded by electroosmotic flow allowed nanoparticles 50-500 nm in size, including EVs, to be precisely separated and enriched in a continuous manner. By observation of the flow behavior of nanoparticles, we found that electroosmotic flow velocity in the nanopillar arrays did not solely depend on counterion mobility on the surface of nanopillar chips, but rather showed a parabolic flow profile. This hydrodynamic pressure-free and easy-to-use separation and enrichment technique, which requires only electrode insertion into the reservoirs and electric field application, may thus serve as a promising technique for future precise and accurate EV analysis, reflecting both size and composition for research and potential clinical diagnostic applications.
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U2 - 10.1021/acs.analchem.8b05538
DO - 10.1021/acs.analchem.8b05538
M3 - Article
C2 - 31035752
AN - SCOPUS:85066920333
SN - 0003-2700
VL - 91
SP - 6514
EP - 6521
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 10
ER -