Parallel Label-Free Isolation of Cancer Cells Using Arrays of Acoustic Microstreaming Traps

被引:42
作者
Lu, Xiaolong [1 ,2 ]
Martin, Aida [1 ]
Soto, Fernando [1 ]
Angsantikul, Pavimol [1 ]
Li, Jinxing [1 ]
Chen, Chuanrui [1 ]
Liang, Yuyan [1 ]
Hu, Junhui [2 ]
Zhang, Liangfang [1 ]
Wang, Joseph [1 ]
机构
[1] Univ Calif San Diego, Dept Nanoengn, La Jolla, CA 92093 USA
[2] Nanjing Univ Aeronaut & Astronaut, State Key Lab Mech & Control Mech Struct, Nanjing 210016, Jiangsu, Peoples R China
来源
ADVANCED MATERIALS TECHNOLOGIES | 2019年 / 4卷 / 02期
基金
中国国家自然科学基金;
关键词
acoustic microstreaming; cancer cells; label-free; parallel isolation; trapping methodology; CIRCULATING TUMOR-CELLS; CONTINUOUS PARTICLE SEPARATION; EFFICIENT CAPTURE; MANIPULATION; CLUSTERS; RELEASE;
D O I
10.1002/admt.201800374
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A new parallel label-free isolation platform for isolating cancer cells (>10 mu m) from biological samples using an array of acoustic microstreaming traps is demonstrated. The new microstreaming trapping platform offers high isolation efficiency and treatment in spiked diluted (1:2) blood samples without labeling, extra processing steps or sheath flows (common to other label-free cell-separation methods), hence, simplifying the microfluidic set-up and operation. The versatility of this label-free method is illustrated by the size-dependent isolation of synthetic colloids and by three different models of breast cancer cells, showing a remarkably high isolation efficiency (95 +/- 5%), being approximate to 100% for MCF-7. Extensive experimental data and theoretical simulations confirm that the local acoustic microstreaming produced by the micropillar trap can discriminate and isolate microparticles based solely on their size. Moreover, the parallel isolation generated by the trap array arrangement is capable of effectively improving the capturing efficiency. The tunable and reversible properties of the acoustic microstreaming allow for cell capturing and optical detection within the trapping area, followed by cell release, enrichment, and collection for further studies. This label-free trapping strategy can open numerous new opportunities for rapid and sensitive detection and capture of cancer cells in biological samples for meaningful clinical applications.
引用
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页数:9
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