Hybrid negative enrichment of circulating tumor cells from whole blood in a 3D-printed monolithic device

被引:36
|
作者
Chu, Chia-Heng [1 ]
Liu, Ruxiu [1 ]
Ozkaya-Ahmadov, Tevhide [1 ]
Boya, Mert [1 ]
Swain, Brandi E. [1 ]
Owens, Jacob M. [2 ]
Burentugs, Enerelt [3 ]
Bilen, Mehmet Asim [4 ,5 ]
McDonald, John F. [6 ,7 ]
Sarioglu, A. Fatih [1 ,5 ,7 ,8 ]
机构
[1] Georgia Inst Technol, Sch Elect & Comp Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[4] Emory Univ, Sch Med, Dept Hematol & Med Oncol, Atlanta, GA USA
[5] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[6] Georgia Inst Technol, Sch Biol Sci, Atlanta, GA 30332 USA
[7] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[8] Georgia Inst Technol, Inst Elect & Nanotechnol, Atlanta, GA 30332 USA
关键词
BREAST-CANCER PATIENTS; LABEL-FREE; IMMUNOMAGNETIC ENRICHMENT; EFFICIENT CAPTURE; DENSITY; MICROFLUIDICS; METASTASIS; COLLECTION; SIZE; FLOW;
D O I
10.1039/c9lc00575g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Isolation and analysis of circulating tumor cells (CTCs) from blood samples present exciting opportunities for basic cancer research and personalized treatment of the disease. While microchip-based negative CTC enrichment offers both sensitive microfluidic cell screening and unbiased selection, conventional microchips are inherently limited by their capacity to deplete a large number of normal blood cells. In this paper, we use 3D printing to create a monolithic device that combines immunoaffinity-based microfluidic cell capture and a commercial membrane filter for negative enrichment of CTCs directly from whole blood. In our device, stacked layers of chemically-functionalized microfluidic channels capture millions of white blood cells (WBCs) in parallel without getting saturated and the leuko-depleted blood is post-filtered with a 3 mu m-pore size membrane filter to eliminate anucleated blood cells. This hybrid negative enrichment approach facilitated direct extraction of viable CTCs off the chip on a membrane filter for downstream analysis. Immunofluorescence imaging of enriched cells showed similar to 90% tumor cell recovery rate from simulated samples spiked with prostate, breast or ovarian cancer cells. We also demonstrated the feasibility of our approach for processing clinical samples by isolating prostate cancer CTCs directly from a 10 mL whole blood sample.
引用
收藏
页码:3427 / 3437
页数:11
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