2007
DOI: 10.1007/s10529-007-9451-1
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Separation of apoptotic cells using a microfluidic device

Abstract: A highly sensitive microfluidic device has been developed to separate apoptotic cells. Apoptotic Jurkat cells were selectively labeled with magnetic beads (0.8 microm diam) using the C2A protein which recognizes phosphatidylserine. The cell mixture was flowed through a microfluidic channel and apoptotic cells were separated by a 0.3 T permanent magnet. Separations using our device showed 96% agreement with those of a commercial flow cytometer, indicating our device can be used to sort apoptotic cells in a mini… Show more

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Cited by 17 publications
(5 citation statements)
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“… 15 , 16 Meanwhile, the magnetophoresis of live cells has found widespread application, ranging from basic quantification of nanomaterials 17 to the detection and isolation of bacteria in water. 18 , 19 The manipulation of whole eukaryotic cells using magnetic nanostructures is especially powerful in microfluidic structures, where local magnetic forces can be applied efficiently, 20 , 21 and different cell types can be sorted, 22 , 23 such as apoptotic cells 24 or specific cancer cells. 25 , 26 In order to assess the uptake mechanisms used by the cells, 17 , 27 and to find out about physiological consequences 28 and potential cytotoxicity 29 during the modification of eukaryotic cells with magnetic nanomaterials, it is necessary to understand the interaction of magnetic nanostructures with the cellular biomolecules and their behavior in the cell.…”
Section: Introductionmentioning
confidence: 99%
“… 15 , 16 Meanwhile, the magnetophoresis of live cells has found widespread application, ranging from basic quantification of nanomaterials 17 to the detection and isolation of bacteria in water. 18 , 19 The manipulation of whole eukaryotic cells using magnetic nanostructures is especially powerful in microfluidic structures, where local magnetic forces can be applied efficiently, 20 , 21 and different cell types can be sorted, 22 , 23 such as apoptotic cells 24 or specific cancer cells. 25 , 26 In order to assess the uptake mechanisms used by the cells, 17 , 27 and to find out about physiological consequences 28 and potential cytotoxicity 29 during the modification of eukaryotic cells with magnetic nanomaterials, it is necessary to understand the interaction of magnetic nanostructures with the cellular biomolecules and their behavior in the cell.…”
Section: Introductionmentioning
confidence: 99%
“…Models of microfluidic magneto-affinity separation are limited in the current literature. Past theoretical models may be divided into two types: capture of magnetic particles only (Chronis et al, 2001;Fukui et al, 2004;Hoffmann and Franzreb, 2004;Warnke, 2003), and capture of cells Frazier, 2005, 2006;Kim et al, 2007;Nan Xia et al, 2006). All previous theoretical studies incorporate basic magnetic and hydrodynamic forces.…”
Section: Introductionmentioning
confidence: 99%
“…Cell separation technology using microfluidic devices has emerged as an efficient technology that allows the user to purify target cells from a variety of environmental and biological samples, which can then be isolated and collected for downstream testing. Numerous techniques have been developed to achieve this purpose, including magnetophoretic , , hydrodynamic , , and acoustic methods. Dielectrophoresis (DEP), the translational motion of charge neutral matter caused by polarization effects in nonuniform electric fields , is a recently emerging technique that can separate cells in microfluidic devices rapidly because low voltages produce significant and contactless forces on cells without any modification or labeling .…”
Section: Introductionmentioning
confidence: 99%