DocumentCode :
187122
Title :
Glucose characterization based on electrochemical impedance spectroscopy
Author :
Olarte, Oscar ; Barbe, K. ; Van Moer, Wendy ; Van Ingelgem, Yves
Author_Institution :
Dept. ELEC, Vrije Univ. Brussel, Brussels, Belgium
fYear :
2014
fDate :
12-15 May 2014
Firstpage :
833
Lastpage :
837
Abstract :
In this paper an equivalent circuit model is employed in the characterization of the impedance measurements of saline solutions at physiological glucose concentrations. The impedance data are obtained using a three electrodes cell configuration since it allows measuring the potential accurately in the working electrode independently from the counter electrode. As excitation signal an odd random phase multisine is employed which allows identifying the best linear approximation, the noise level and the non-linear distortions present in the system. The results show a significant change in the impedance as a function of the glucose at the interphase electrode-electrolyte as well as in the bulk solution. This is an important step towards the development of glucose measurement systems based in electrochemical impedance spectroscopy (EIS).
Keywords :
biomedical measurement; chemical variables measurement; electric impedance measurement; electrochemical impedance spectroscopy; equivalent circuits; sugar; EIS; electrochemical impedance spectroscopy; electrodes cell configuration; equivalent circuit model; glucose characterization; glucose measurement system; impedance measurement; interphase electrode-electrolyte; linear approximation; nonlinear distortion; odd random phase multisine; physiological glucose concentration; saline solution; Electrodes; Equivalent circuits; Impedance; Impedance measurement; Integrated circuit modeling; Physiology; Sugar;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Instrumentation and Measurement Technology Conference (I2MTC) Proceedings, 2014 IEEE International
Conference_Location :
Montevideo
Type :
conf
DOI :
10.1109/I2MTC.2014.6860860
Filename :
6860860
Link To Document :
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