Label-free detection of multidrug resistance in K562 cells through isolated 3D-electrode dielectrophoresis

被引:20
作者
Demircan, Yagmur [1 ,2 ]
Koyuncuoglu, Aziz [2 ,3 ]
Erdem, Murat [4 ]
Ozgur, Ebru [2 ]
Gunduz, Ufuk [4 ]
Kulah, Haluk [1 ,2 ]
机构
[1] METU, Dept Elect & Elect Engn, Ankara, Turkey
[2] METU MEMS Res & Applicat Ctr, Ankara, Turkey
[3] METU, Dept Mech Engn, Ankara, Turkey
[4] METU, Dept Biol, Ankara, Turkey
关键词
3D-electrode; Isolated electrode dielectrophoresis; Leukemia; Multidrug resistance; Parylene; Trapping; CONTACTLESS DIELECTROPHORESIS; DIELECTRIC-PROPERTIES; EARLY-DIAGNOSIS; LEUKEMIC-CELLS; P-GLYCOPROTEIN; CANCER-CELLS; ELECTROROTATION; MANIPULATION; SENSITIVITY; IMATINIB;
D O I
10.1002/elps.201400391
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dielectrophoresis (DEP), a technique used to separate particles based on different sizes and/or dielectric properties under nonuniform electric field, is a promising method to be applied in label-free, rapid, and effective cell manipulation and separation. In this study, a microelectromechanical systems-based, isolated 3D-electrode DEP device has been designed and implemented for the label-free detection of multidrug resistance in K562 leukemia cells, based on the differences in their cytoplasmic conductivities. Cells were hydrodynamically focused to the 3D-electrode arrays, placed on the side walls of the microchannel, through V-shaped parylene-C obstacles. 3D-electrodes extruded along the z-direction provide uniformly distributed DEP force through channel depth. Cell suspension containing resistant and sensitive cancer cells with 1:100 ratio was continuously flown through the channel at a rate of 10 L/min. Detection was realized at 48.64 MHz, the cross-over frequency of sensitive K562 cells, at which sensitive cells flow with the fluid, while the resistant ones are trapped by positive DEP force. Device can be operated at considerably low voltages (<9 V-pp). This is achieved by means of a very thin (0.5 m) parylene coating on electrodes, providing the advantages offered by the isolation of electrodes from the sample, while the working voltage can still be kept low. Results prove that the presented DEP device can provide an efficient platform for the detection of multidrug resistance in leukemia, in a label-free manner.
引用
收藏
页码:1149 / 1157
页数:9
相关论文
共 35 条
[1]   Biomarkers and biosensors for the early diagnosis of lung cancer [J].
Altintas, Zeynep ;
Tothill, Ibtisam .
SENSORS AND ACTUATORS B-CHEMICAL, 2013, 188 :988-998
[2]  
[Anonymous], 2010, MULTIDRUG RESISTANCE
[3]   Ionic currents in multidrug resistant K562 human leukemic cells [J].
Assef, YA ;
Cavarra, SM ;
Damiano, AE ;
Ibarra, C ;
Kotsias, BA .
LEUKEMIA RESEARCH, 2005, 29 (09) :1039-1047
[4]   Mechanisms of cellular resistance to imatinib in human chronic myeloid leukemia cells [J].
Baran, Yusuf ;
Ural, Ali Ugur ;
Gunduz, Ufuk .
HEMATOLOGY, 2007, 12 (06) :497-503
[5]   High sensitivity three-dimensional insulator-based dielectrophoresis [J].
Braff, William A. ;
Pignier, Alexandre ;
Buie, Cullen R. .
LAB ON A CHIP, 2012, 12 (07) :1327-1331
[6]   Extraction of dielectric properties of multiple populations from dielectrophoretic collection spectrum data [J].
Broche, LM ;
Labeed, FH ;
Hughes, MP .
PHYSICS IN MEDICINE AND BIOLOGY, 2005, 50 (10) :2267-2274
[7]   An integrated nanoliter DNA analysis device [J].
Burns, MA ;
Johnson, BN ;
Brahmasandra, SN ;
Handique, K ;
Webster, JR ;
Krishnan, M ;
Sammarco, TS ;
Man, PM ;
Jones, D ;
Heldsinger, D ;
Mastrangelo, CH ;
Burke, DT .
SCIENCE, 1998, 282 (5388) :484-487
[8]  
Campana D, 2012, Leuk Suppl, V1, pS3, DOI 10.1038/leusup.2012.5
[9]   Continuous particle separation based on electrical properties using alternating current dielectrophoresis [J].
Cetin, Barbaros ;
Li, Dongqing .
ELECTROPHORESIS, 2009, 30 (18) :3124-3133
[10]   Biophysical characterization of MDR breast cancer cell lines reveals the cytoplasm is critical in determining drug sensitivity [J].
Coley, Helen M. ;
Labeed, Fatima H. ;
Thomas, Hilary ;
Hughes, Michael P. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2007, 1770 (04) :601-608