Effect of Media Conductivity on High Frequency Dielectrophoretic Response

Author(s):  
Hanieh Hadady ◽  
Johnson J. Wong ◽  
Sage R. Hiibel ◽  
Emil J. Geiger

A method was developed for analyzing the high frequency dielectrophoresis (>20 MHz) response of microalgal cells with different lipid content on the basis of media conductivities. At these frequencies, the DEP response is expected to depend primarily on the dielectric properties of the cytoplasm. The medium used to perform DEP experiments has an important influence on their outcome since all properties are measured in relation to the medium, therefore its properties must be tightly controlled. This method is label free and only uses electric fields, and thus it is suitable for many other applications in the medical field. Chlamydomonas reinhardtii cells were cultured in regular medium and then the same cells were cultured under nitrogen-free conditions to accumulate neutral (non-polar) lipids. To measure the upper crossover frequency, two thin, needle shaped electrodes (100 nm thick) were patterned onto a glass slide using standard micro-technology processes and the motion of the cells was observed as an AC signal was swept from 20–80 MHz at ∼30Vpp (Volt peak to peak). Cells were injected to the microelectrode array in different medium conductivities that were adjusted by sodium chloride. The upper crossover frequencies of N-free cells in different media conductivities were measured. It was found that when the solution conductivity was between 4 ± 2 μs/cm and 106 ± 1 μS/cm and the operating frequency was between 20 and 80 MHz, the upper crossover frequency of the microalgae increased as the medium conductivity increased. The lipid content was verified via fluorescence microscopy and MATLAB image processing.

2007 ◽  
Vol 12 (5) ◽  
pp. 311-317 ◽  
Author(s):  
Vindhya Kunduru ◽  
Shalini Prasad

We demonstrate a technique to detect protein biomarkers contained in vulnerable coronary plaque using a platform-based microelectrode array (MEA). The detection scheme is based on the property of high specificity binding between antibody and antigen similar to most immunoassay techniques. Rapid clinical diagnosis can be achieved by detecting the amount of protein in blood by analyzing the protein's electrical signature. Polystyrene beads which act as transportation agents for the immobile proteins (antigen) are electrically aligned by application of homogenous electric fields. The principle of electrophoresis is used to produce calculated electrokinetic movement among the anti-C-reactive protein (CRP), or in other words antibody funtionalized polystyrene beads. The electrophoretic movement of antibody-functionalized polystyrene beads results in the formation of “Microbridges” between the two electrodes of interest which aid in the amplification of the antigen—antibody binding event. Sensitive electrical equipment is used for capturing the amplified signal from the “Microbridge” which essentially behaves as a conducting path between the two electrodes. The technique circumvents the disadvantages of conventional protein detection methods by being rapid, noninvasive, label-free, repeatable, and inexpensive. The same principle of detection can be applied for any receptor—ligand-based system because the technique is based only on the volume of the analyte of interest. Detection of the inflammatory coronary disease biomarker CRP is achieved at concentration levels spanning over the lower microgram/milliliter to higher order nanogram/milliliter ranges.


1974 ◽  
Vol 9 (16) ◽  
pp. 650-652 ◽  
Author(s):  
U. Carretta ◽  
E. Sindoni ◽  
U. Tartari

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