Lectin-mediated microfluidic capture and release of leukemic lymphocytes from whole blood

被引:12
|
作者
Vickers, Dwayne A. L. [1 ]
Hincapie, Marina [2 ,3 ]
Hancock, William S. [2 ,3 ]
Murthy, Shashi K. [1 ]
机构
[1] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
[2] Northeastern Univ, Barnett Inst, Boston, MA 02115 USA
[3] Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USA
关键词
Microfluidics; Lectins; Cell capture; Cell adhesion; Blood; Leukemia; CELLS; BINDING; FLOW;
D O I
10.1007/s10544-011-9527-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Lectins are a group of proteins that bind specifically and reversibly to mono- and oligosaccharide carbohydrate structures that are present on the surfaces of mammalian cells. The use of lectins as capture agents in microfluidic channels was examined with a focus on cells associated with T and B lymphocytic leukemia. In addition to examining the adhesion of Jurkat T and Raji B lymphocytes to a broad panel of lectins, this work also examined the capture of these cells from whole blood. Captured T and B lymphocytes were eluted from the microfluidic devices with a solution of the lectin's inhibiting sugar. The capture and release steps were accomplished in under 1 h. The significance of this work lies within the realm of low-cost capture of abundant target cells with non-stimulatory elution capability.
引用
收藏
页码:565 / 571
页数:7
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