Nanoscale lateral displacement arrays for the separation of exosomes and colloids down to 20 nm

被引:486
作者
Wunsch, Benjamin H. [1 ]
Smith, Joshua T. [1 ]
Gifford, Stacey M. [1 ]
Wang, Chao [1 ,4 ,5 ]
Brink, Markus [1 ]
Bruce, Robert L. [1 ]
Austin, Robert H. [2 ]
Stolovitzky, Gustavo [1 ,3 ]
Astier, Yann [1 ,6 ]
机构
[1] IBM TJ Watson Res Ctr, Yorktown Hts, NY 10598 USA
[2] Princeton Univ, Dept Phys, Princeton, NJ 08540 USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[4] Arizona State Univ, Sch Elect Comp & Energy Engn, Tempe, AZ 82587 USA
[5] Arizona State Univ, Biodesign Ctr Mol Design & Biomimet, Tempe, AZ 82587 USA
[6] Roche Mol Syst, Pleasanton, CA 94588 USA
关键词
PARTICLE SEPARATION; EFFICIENCY; SPHERE; CELLS;
D O I
10.1038/nnano.2016.134
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Deterministic lateral displacement (DLD) pillar arrays are an efficient technology to sort, separate and enrich micrometre-scale particles, which include parasites', bacterial, blood cells(3) and circulating tumour cells in blood(4). However, this technology has not been translated to the true nanoscale, where it could function on biocolloids, such as exosomes. Exosomes, a key target of 'liquid biopsies', are secreted by cells and contain nucleic acid and protein information about their originating tissues(5). One challenge in the study of exosome biology is to sort exosomes by size and surface markers(6,7). We use manufacturable silicon processes to produce nanoscale DLD (nano-DLD) arrays of uniform gap sizes ranging from 25 to 235 nm. We show that at low Peclet (Pe) numbers, at which diffusion and deterministic displacement compete, nano-DLD arrays separate particles between 20 to 110 nm based on size with sharp resolution. Further, we demonstrate the size-based displacement of exosomes, and so open up the potential for on-chip sorting and quantification of these important biocolloids.
引用
收藏
页码:936 / 940
页数:5
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