DocumentCode :
1801315
Title :
Whole cell electrical impedance spectroscopy for studying ion channel activity
Author :
Han, Arum ; Moss, Eilcen ; Frazier, A. Bruno
Author_Institution :
Sch. of Electr. & Comput. Eng., Georgia Inst. of Technol., Atlanta, GA, USA
Volume :
2
fYear :
2005
fDate :
5-9 June 2005
Firstpage :
1704
Abstract :
In this work, the micro electrophysiological analysis system (μ-EPAS) is used to study the ion channel activity of single cells. The μ-EPAS has been designed, fabricated, and characterized for this application. The whole cell analysis system has the capability to perform patch clamping, electrical impedance spectroscopy (EIS), and general extracellular recording using integrated, multi-electrode configurations within a single analysis cavity. Bovine chromaffin cells were used as the target cell to demonstrate and characterize the system. Whole cell impedance measurements were taken over a frequency range of 100 Hz to 5.0 MHz. The impedance signatures of bovine chromaffin cells with: i) the K+ channels blocked; ii) the Ca2+ channels blocked; and iii) unmodified cells were measured and analyzed.
Keywords :
bioelectric phenomena; biomedical measurement; cellular biophysics; electric impedance measurement; micromechanical devices; 100 to 5E6 Hz; bovine chromaffin cells; cell analysis system; cell impedance measurements; electrophysiology; extracellular recording; ion channel activity; microelectrophysiological analysis system; multielectrode configurations; patch clamping; single analysis cavity; whole cell electrical impedance spectroscopy; Bovine; Clamps; Drugs; Electrochemical impedance spectroscopy; Electrodes; Electrophysiology; Extracellular; Impedance measurement; Performance analysis; Sensor arrays;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Solid-State Sensors, Actuators and Microsystems, 2005. Digest of Technical Papers. TRANSDUCERS '05. The 13th International Conference on
Print_ISBN :
0-7803-8994-8
Type :
conf
DOI :
10.1109/SENSOR.2005.1497419
Filename :
1497419
Link To Document :
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