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. Author manuscript; available in PMC: 2012 Apr 1.
Published in final edited form as: Chem Eng Sci. 2011 Apr 1;66(7):1508–1522. doi: 10.1016/j.ces.2010.09.012

Table 2. Electrokinetic cell fractionation/isolation.

Application Cell Type Modeled Cell Type Used Carrier Media Off-line Processing Experimental Parameters Efficiency Enrichment Purity DEP Technique Reference
L. monocytogenes L. innocua DI water, 2 μS/cm; 105 cells/mL Cell counting 1 Vpp, 50 kHz 90% IDA Li and Bashir (2002)
Pathogen detection L. monocytogenes L. monocytogenes DI water, 1-15 μS/cm; 102-103 cells/mL Cell counting 0.2 μL/min, 800 μm/s; 20 Vpp, 1 MHz 87-92% IDA + IC Yang et al. (2006)
B. anthracis B. subtilis DI water, 5×10−4S/m; 3.8×106 cells/mL Measure absorbance 100 μL/min; 40 Vpp, 100 kHz IDA Gadish and Voldman (2006)
B. anthracis B. subtilis DI water, 7.6 mS/m; 9.9×107 spores/mL, 2.1×107 diesel particles/mL Hemacytometer 0.5-4 mL/hr, 94 μm/s; 10 Vpp, 1 MHz na na ≤ 60% IDA Fatoyinbo et al. (2007)
B. anthracis B. anthracis DI water, 2-3 μS/cm; 107-109 spores/mL Cell counting 0.2 μL/min, 40 cm/min; 20 Vpp, 100 kHz 90% na na IDA Liu et al. (2007b)
Plasmodium falciparum Malaria-infected erythrocytes Sucrose buffer, 22-55 mS/m; 107 cells/mL Cell counting 5Vpp, 200 kHz 90% 50-200× na Castellated Gascoyne et al. (2002)
na B. cereus, E. coli, L. monocytogenes Mannitol + PBS, 180 μS/cm; 4 μL blood + 1 μL of 106 B. cereus or 7×105 E. coli or 106 L. monocytogenes PCR amplification 10 Vpp, 10 kHz ≤97% na na Castellated Huang et al. (2003)
na E. coli DI water, 10-20 μS/cm; 105 cells/mL Cell counting 100 Pa; 2000 V/cm 90+% 3000× na iDEP Lapizco-Encinas et al. (2005)
na E. coli PBS, 0.5 mS/m; 9.3×103 cells/mL Cell counting 100 μL/min; 128 V/mm, 300 kHz 66% na na iDEP Cho et al. (2009)

Cancer cell isolation Lung cancer A549-luc-C8 DMEM buffer, 72 μS/cm Flow cytometry 3 μL/min; 15 Vpp, 16 MHz 81-84% na na Castellated Tai et al. (2007)
Breast cancer MDA231 Sucrose buffer; 107 malignant, 3×107 normal cells/mL Cell counting 5 Vpp, 200 kHz na na 95% Castellated Becker et al. (1995)
Breast cancer MDA-435 Sucrose buffer, 56 mS/m; 5×106 cells/mL, 2:3 ratio of MDA-435:RBCs Cell counting 0.5 mL/min, 780 μm/s; 1.4 Vpp, 5 kHz na na 98% FFF Yang et al. (1999)
Breast cancer MDA-435, -468, -231 cells Sucrose buffer, 30 mS/m; 105-106 cells/mL, 1:1000 ratio of tumor cell to PBMNs Cell counting 1.5 mL/min; 2.8 Vpp, 60 kHz ≤92% na na FFF Gascoyne et al. (2009)
Breast cancer MDA-435, CD34+ stem cells Sucrose buffer, 10 mS/m; 106 cells/mL, 3:2 ratio of CD34+ to MDA-435 Flow cytometry 2 mL/min; 4 Vpp, 40 kHz na na 96-99% FFF Huang et al. (1999)
Breast cancer MDA-MB-231 PBS, 100-200 mS/m; 106 cells/mL Flow cytometry 200-400 μL/hr; 20 Vpp, 500 kHz na 4.4× 96% Angled electrodes Kim et al. (2007)
Leukemia THP-1 Sucrose buffer, 110-115 μS/cm; 106 cells/mL Cell counting 0.02 mL/hr, 222 μm/s; 20-50 Vrms, 200-500 kHz 90+% na na Contactless DEP Shafiee et al. (2010)

Blood fractionation or enrichment Leukocytes Leukocytes Sucrose buffer, 10 mS/m; 2×106 cells/mL, 1:1 ratio Flow cytometry 2 mL/min; 4Vpp, 20-50 kHz na na 87-98% FFF Yang et al. (2000)
Leukocytes Leukocytes GIT medium, 13 mS/cm; 5×106 cells/mL Cell counting 1.5 μL/min; 20 Vpp, 1 MHz 80% na na FFF + IC Hashimoto et al. (2009)
Leukocytes MDA-435, CD34+ stem cells Sucrose buffer, 10 mS/m; Separation: 1.2×106 cells/mL, Leukocyte enrichment: 5×106 cells/mL Flow cytometry Separation: 2 mL/min, Leukocyte enrichment: 0.5 mL/min; 4 Vpp, 40 kHz 55-75% na 92-99% FFF Wang et al. (2000)
Malaria Erythrocytes infected with B. bovis PBS, 60 mS/m Cell counting 500 μm/s; 4.7-9 Vrms, 90 kHz-4 MHz na na FFF Braschler et al. (2008)
Malaria Erythrocytes infected with P. falciparum Sucrose buffer, 0.055 S/m; 2000 cells with 5% parasitized cells Cell counting 3 Vpp, 2 MHz na 1000× 90% twDEP Gascoyne et al. (2002)
Platelets Concentrated platelets + whole blood Sucrose buffer, 50 mS/m; 107 cells/mL Flow cytometry 150 μL/hr; 6.6 mm/s; 100 Vpp, 1 MHz na 5.3× 95% Angled electrodes Pommer et al. (2008)