The authors would like to thank Herman Liggesmeyer and Marvin Bende for their expert advice in electrotechnics and informatics.

1. Assembly of a basic volt-amperemeter for TEER measurement
<ol>
	<li>Prepare a standard USB charger as the 5 V D.C. power supply, a USB extension cord, a microcontroller that will be used as a programmable square wave generator, two standard multimeters that are able to measure alternating current and voltage as root mean square (True-RMS), four cables with banana plugs, a telephone extension cord with a RJ14 female connector including six pins with the inner four wired (6P4C), two short cables, a luster terminal, a ...

<ol>
	<li>Matter, K., Balda, M. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Functional+analysis+of+tight+junctions.">Functional analysis of tight junctions.</a> Methods. 30, 228-234 (2003).</li><li>Srinivasan, B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=TEER+measurement+techniques+for+in+vitro+barrier+model+systems.">TEER measurement techniques for in vitro barrier model systems.</a> Journal of Laboratory Automation. 20, 107-126 (2015).</li><li>Daniels, B. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Immortalized+human+cerebral+microvascular+endothelial+cells+maintain+the+properties+of+primary+cells+in+an+in+vitro+model+of+immune+migration+across+the+blood+brain+barrier.">Immortalized human cerebral microvascular endothelial cells maintain the properties of primary cells in an in vitro model of immune migration across the blood brain barrier.</a> Journal of Neuroscience Methods. 212, 173-179 (2013).</li><li>Weksler, B. B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Blood-brain+barrier-specific+properties+of+a+human+adult+brain+endothelial+cell+line.">Blood-brain barrier-specific properties of a human adult brain endothelial cell line.</a> Federation of American Societies for Experimental Biology Journal. 19, 1872-1874 (2005).</li><li>Lippmann, E. S., Al-Ahmad, A., Azarin, S. M., Palecek, S. P., Shusta, E. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+retinoic+acid-enhanced,+multicellular+human+blood-brain+barrier+model+derived+from+stem+cell+sources.">A retinoic acid-enhanced, multicellular human blood-brain barrier model derived from stem cell sources.</a> Scientific Reports. 4, 4160 (2014).</li><li>Stins, M. F., Badger, J., Sik Kim, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bacterial+invasion+and+transcytosis+in+transfected+human+brain+microvascular+endothelial+cells.">Bacterial invasion and transcytosis in transfected human brain microvascular endothelial cells.</a> Microbial Pathogenesis. 30, 19-28 (2001).</li><li>Muruganandam, A., Herx, L. M., Monette, R., Durkin, J. P., Stanimirovic, D. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+of+immortalized+human+cerebromicrovascular+endothelial+cell+line+as+an+in+vitro+model+of+the+human+blood-brain+barrier.">Development of immortalized human cerebromicrovascular endothelial cell line as an in vitro model of the human blood-brain barrier.</a> Federation of American Societies for Experimental Biology Journal. 11, 1187-1197 (1997).</li><li>Ishiwata, I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Establishment+and+characterization+of+a+human+malignant+choroids+plexus+papilloma+cell+line+(HIBCPP).">Establishment and characterization of a human malignant choroids plexus papilloma cell line (HIBCPP).</a> Human Cell. 18, 67-72 (2005).</li><li>Dinner, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+Choroid+Plexus+Epithelial+Cell-based+Model+of+the+Human+Blood-Cerebrospinal+Fluid+Barrier+to+Study+Bacterial+Infection+from+the+Basolateral+Side.">A Choroid Plexus Epithelial Cell-based Model of the Human Blood-Cerebrospinal Fluid Barrier to Study Bacterial Infection from the Basolateral Side.</a> Journal of Visualized Experiments. , (2016).</li><li>Schwerk, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polar+invasion+and+translocation+of+Neisseria+meningitidis+and+Streptococcus+suis+in+a+novel+human+model+of+the+blood-cerebrospinal+fluid+barrier.">Polar invasion and translocation of Neisseria meningitidis and Streptococcus suis in a novel human model of the blood-cerebrospinal fluid barrier.</a> PLoS One. 7, e30069 (2012).</li><li>Tenenbaum, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polar+bacterial+invasion+and+translocation+of+Streptococcus+suis+across+the+blood-cerebrospinal+fluid+barrier+in+vitro.">Polar bacterial invasion and translocation of Streptococcus suis across the blood-cerebrospinal fluid barrier in vitro.</a> Cellular Microbiology. 11, 323-336 (2009).</li><li>Gath, U., Hakvoort, A., Wegener, J., Decker, S., Galla, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Porcine+choroid+plexus+cells+in+culture:+expression+of+polarized+phenotype,+maintenance+of+barrier+properties+and+apical+secretion+of+CSF-components.">Porcine choroid plexus cells in culture: expression of polarized phenotype, maintenance of barrier properties and apical secretion of CSF-components.</a> European Journal of Cell Biology. 74, 68-78 (1997).</li><li>Haselbach, M., Wegener, J., Decker, S., Engelbertz, C., Galla, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Porcine+Choroid+plexus+epithelial+cells+in+culture:+regulation+of+barrier+properties+and+transport+processes.">Porcine Choroid plexus epithelial cells in culture: regulation of barrier properties and transport processes.</a> Microscopy Research and Technique. 52, 137-152 (2001).</li><li>Strazielle, N., Ghersi-Egea, J. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physiology+of+blood-brain+interfaces+in+relation+to+brain+disposition+of+small+compounds+and+macromolecules.">Physiology of blood-brain interfaces in relation to brain disposition of small compounds and macromolecules.</a> Molecular Pharmaceutics. 10, 1473-1491 (2013).</li><li>Hilgendorf, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Caco-2+versus+Caco-2/HT29-MTX+co-cultured+cell+lines:+permeabilities+via+diffusion,+inside-+and+outside-directed+carrier-mediated+transport.">Caco-2 versus Caco-2/HT29-MTX co-cultured cell lines: permeabilities via diffusion, inside- and outside-directed carrier-mediated transport.</a> Journal of Pharmaceutical Sciences. 89, 63-75 (2000).</li><li>Mathia, N. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Permeability+characteristics+of+calu-3+human+bronchial+epithelial+cells:+in+vitro-in+vivo+correlation+to+predict+lung+absorption+in+rats.">Permeability characteristics of calu-3 human bronchial epithelial cells: in vitro-in vivo correlation to predict lung absorption in rats.</a> Journal of Drug Targeting. 10, 31-40 (2002).</li><li>Fuchs, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differentiation+of+human+alveolar+epithelial+cells+in+primary+culture:+morphological+characterization+and+synthesis+of+caveolin-1+and+surfactant+protein-C.">Differentiation of human alveolar epithelial cells in primary culture: morphological characterization and synthesis of caveolin-1 and surfactant protein-C.</a> Cell and Tissue Research. 311, 31-45 (2003).</li><li>Furie, M. B., Cramer, E. B., Naprstek, B. L., Silverstein, S. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cultured+endothelial+cell+monolayers+that+restrict+the+transendothelial+passage+of+macromolecules+and+electrical+current.">Cultured endothelial cell monolayers that restrict the transendothelial passage of macromolecules and electrical current.</a> The Journal of Cell Biology. 98, 1033-1041 (1984).</li><li>Hidalgo, I. J., Raub, T. J., Borchardt, R. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Characterization+of+the+human+colon+carcinoma+cell+line+(Caco-2)+as+a+model+system+for+intestinal+epithelial+permeability.">Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability.</a> Gastroenterology. 96, 736-749 (1989).</li><li>Yeste, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Geometric+correction+factor+for+transepithelial+electrical+resistance+measurements+in+Transwell+and+microfluidic+cell+cultures.">Geometric correction factor for transepithelial electrical resistance measurements in Transwell and microfluidic cell cultures.</a> Journal of Physics D Applied Physics. 49 (37), 3754 (2016).</li><li>Northrup, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=VI:+The+Measurement+of+Low+Resistance.">VI: The Measurement of Low Resistance.</a> Methods of Measuring Electrical Resistance. , 100-131 (1912).</li><li>Li, H., Sheppard, D. N., Hug, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transepithelial+electrical+measurements+with+the+Ussing+chamber.">Transepithelial electrical measurements with the Ussing chamber.</a> Journal of Cystic Fibrosis. 3 (Suppl 2), 123-126 (2004).</li><li>Griep, L. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=BBB+on+chip:+microfluidic+platform+to+mechanically+and+biochemically+modulate+blood-brain+barrier+function.">BBB on chip: microfluidic platform to mechanically and biochemically modulate blood-brain barrier function.</a> Biomedical Microdevices. 15, 145-150 (2013).</li><li>Esch, M. B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+chip+porous+polymer+membranes+for+integration+of+gastrointestinal+tract+epithelium+with+microfluidic+'body-on-a-chip'+devices.">On chip porous polymer membranes for integration of gastrointestinal tract epithelium with microfluidic 'body-on-a-chip' devices.</a> Biomedical Microdevices. 14, 895-906 (2012).</li><li>. Arduino Web Editor Available from: <a target="_blank" href="https://www.arduino.cc/en/Main/Software">https://www.arduino.cc/en/Main/Software</a> (2019)</li><li>Benson, K., Cramer, S., Galla, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Impedance-based+cell+monitoring:+barrier+properties+and+beyond.">Impedance-based cell monitoring: barrier properties and beyond.</a> Fluids and Barriers of the CNS. 10, 5 (2013).</li><li>Hufnagl, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Time Resolved Transepithelial Impedance Spectroscopy Of Caco 2 Monolayers Relying on Lithographically Patterned Basolateral Electrode Cell Arrays. , (2010).</li><li>Guimer&#224;, A., Gabriel, G., Parramon, D., Calder&#243;n, E., Villa, R., D&#246;ssel, O., Schlegel, W. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Portable+4+Wire+Bioimpedance+Meter+with+Bluetooth+Link.">Portable 4 Wire Bioimpedance Meter with Bluetooth Link.</a> World Congress on Medical Physics and Biomedical Engineering. International Federation of Medical and Biological Engineering Proceedings. 25/7, (2009).</li></ol>

Before a self-made voltammeter can be used in a daily routine, it is essential to check the device for proper function. In our case, a half-time of oscillation of 40 ms (12.5 Hz) was programmed, but the effective oscillation time turned out to be 60 ms (16.7 Hz). This inaccuracy of the microcontroller&#39;s time emitter had no detectable impact on TEER measurements. It might be best to determine the actual frequency using the frequency setting of one of the multimeters. If any deviation is found, the source code can be a...

Epithelial and endothelial cells function as cellular boundaries, separating the apical and basolateral sides of the body. If they are connected through tight junctions, passive substance diffusion through the paracellular spaces is restricted1, resulting in the formation of a selectively permeable barrier. Several artificial barrier systems have been developed2 using microvascular endothelial cells (HBMEC, blood-brain barrier3,4,5,6,7), choroid plexus epithelial cells (HIBCPP/PCPEC, blood-cerebrospinal fluid barrier8,9,10,11,12,13,14), colorectal adenocarcinoma cells (Caco-2, gastrointestinal models15), or airway/alveolar cell lines (pulmonary models16,17). These systems typically consist of cells grown in a monolayer on permeable membranes (i.e., filter insert systems) to allow access to the apical and basolateral sides. It is important that the integrity of the model system matches the in vivo conditions. Hence, several techniques have been developed to analyze barrier function by measuring paracellular diffusion of tracer compounds across the cell layer. These substances include radiolabeled sucrose, dye-labeled albumin, FITC-labeled inulin, or dye-labeled dextrans2. However, chemical dyes can make cells unusable for further experiments. To monitor barrier systems noninvasively, measurement of transepithelial/transendothelial electrical resistance (TEER) across a cellular monolayer can be used2,18,19. Because bipolar electrode systems are influenced by the electrode polarization impedance at the electrode-electrolyte interface, tetrapolar measurements are generally used to overcome this limitation20. The underlaying technique is a four-terminal sensing (4T) that was first described in 1861 by William Thomson (Lord Kelvin)21. In brief, the current is injected by a pair of current-carrying electrodes while a second pair of voltage-sensing electrodes is used to measure the voltage drop20. Nowadays, so-called chopstick electrodes consist of a pair of double electrodes, each containing a silver/silver-chloride pellet for measuring voltage and a silver electrode for passing current2. The electrical impedance is measured between the apical and the basolateral compartment with the cell layer in between (Figure 1). A square wave signal at a frequency of typically 12.5 Hz is applied at the outer electrodes and the resulting alternating current (AC) measured. Additionally, the potential drop across the cell layer is measured by the second (inner) electrode pair. Electrical impedance is then calculated according to Ohm&#39;s law. TEER values are normalized by multiplying impedance and cell layer surface area and are typically expressed as &#937; &#8729; cm2.
There are systems in which cells and electrodes are arranged in a more sophisticated way, but are also based on the 4T measuring principle and can be used with the same measurement devices. EndOhm systems, for example, in which the filter is inserted, contain a chamber and cap with a pair of concentric electrodes with the same structure as the chopstick electrode. The shape of the electrodes allows for a more uniform current density flow across the membrane, thereby reducing variation between readings. Even more complex (but also more accurate) is an Ussing chamber, where a cell layer separates two chambers filled with Ringer&#39;s solution22. The chamber itself can be gassed with oxygen, CO2, or N2, and stirred or supplemented with experimental substances. As ion transport across the cell layer occurs, a potential difference can be measured by two voltage-sensing electrodes near the tissue. This voltage is cancelled out by two current-carrying electrodes placed next to the cell layer. The measured current will then give the net ion transport and the transepithelial resistance, which reflects barrier integrity, can be determined22. TEER measurement can also be applied on body-on-a-chip systems that represent barrier-tissue models23,24. These systems mimic in vivo conditions of the cells and often consist of several types of cells, stacked on top of each other in layers.
The following protocol explains how to set up a cost-effective and reliable voltammeter with programmable output frequency that produces no statistically significant differences in TEER compared to commercially available measurement systems.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>120 kOhm resistor</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Banana plug cables</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Cables</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Chopstick electrode</td>
			<td>Merck Millicell</td>
			<td>MERSSTX01</td>
			<td></td>
		</tr>
		<tr>
			<td>Chopstick electrode (alternative)</td>
			<td>WPI World Precision Instruments</td>
			<td>STX2</td>
			<td></td>
		</tr>
		<tr>
			<td>Crimping tool</td>
			<td></td>
			<td></td>
			<td>General tool</td>
		</tr>
		<tr>
			<td>Digispark / ATtiny85</td>
			<td>AZ-Delivery Vertriebs GmbH</td>
			<td>Digispark Rev.3 Kickstarter</td>
			<td></td>
		</tr>
		<tr>
			<td>DMEM:F12</td>
			<td>Gibco (Thermo Fisher)</td>
			<td>31330038</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal calf serum (FCS)/Fetal Bovine Serum (FBS)</td>
			<td>Life Technologies</td>
			<td>10270106</td>
			<td></td>
		</tr>
		<tr>
			<td>Filter inserts 3&#181;m translucent</td>
			<td>Greiner Bioone</td>
			<td>662631</td>
			<td></td>
		</tr>
		<tr>
			<td>HIBCPP</td>
			<td></td>
			<td></td>
			<td>Hiroshi Ishikawa / Horst Schroten</td>
		</tr>
		<tr>
			<td>Insulation stripper</td>
			<td></td>
			<td></td>
			<td>General tool</td>
		</tr>
		<tr>
			<td>Luster terminal</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Oscilloscope</td>
			<td>HAMEG</td>
			<td>Digital Storage Scope HM 208</td>
			<td></td>
		</tr>
		<tr>
			<td>Plotter</td>
			<td>PHILIPS</td>
			<td>PM 8143 X-Y recorder</td>
			<td></td>
		</tr>
		<tr>
			<td>Software Arduino</td>
			<td>https://www.arduino.cc</td>
			<td>Arduino 1.8.9</td>
			<td></td>
		</tr>
		<tr>
			<td>Soldering iron</td>
			<td></td>
			<td></td>
			<td>General tool</td>
		</tr>
		<tr>
			<td>Soldering lugs</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Telephone cable with RJ14 (6P4C) connector</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Test resistor</td>
			<td>Merck Millicell</td>
			<td>MERSSTX04</td>
			<td></td>
		</tr>
		<tr>
			<td>True-RMS multimeters</td>
			<td>VOLTCRAFT</td>
			<td>VC185</td>
			<td></td>
		</tr>
		<tr>
			<td>USB charger</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>USB extension cord</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
		<tr>
			<td>Voltohmmeter for TEER measurement</td>
			<td>WPI World Precision Instruments</td>
			<td>EVOM</td>
			<td></td>
		</tr>
		<tr>
			<td>Voltohmmeter for TEER measurement (alternative)</td>
			<td>Merck Millicell</td>
			<td>ERS</td>
			<td></td>
		</tr>
		<tr>
			<td>Wire end ferrules</td>
			<td></td>
			<td></td>
			<td>General (generic) equipment</td>
		</tr>
	</tbody>
</table>

a simple approach to perform teer measurements using a self-made volt-amperemeter with programmable output frequency

Transepithelial/endothelial electrical resistance (TEER) has been used since the 1980s to determine confluency and permeability of in vitro barrier model systems. In most cases, chopstick electrodes are used to determine the electric impedance between the upper and lower compartment of a cell culture filter insert system containing cellular monolayers. The filter membrane allows the cells to adhere, polarize, and interact by building tight junctions. This technique has been described with a variety of different cell lines (e.g., cells of the blood-brain barrier, blood-cerebrospinal fluid barrier, or gastrointestinal and pulmonary tract). TEER measurement devices can be readily obtained from different laboratory equipment suppliers. However, there are more cost-effective and customizable solutions imaginable if an appropriate voltammeter is self-assembled. The overall aim of this publication is to set up a reliable device with programmable output frequency that can be used with commercially available chopstick electrodes for TEER measurement.

To compare the operation of a self-assembled voltammeter with its commercially available counterpart, a voltage oscillogram of both devices was recorded.
As shown in Figure 2A, the reference instrument generated a square wave signal with an amplitude of 80 mV and an oscillation time of 80 ms, which corresponds to a frequency of 12.5 Hz, when operating on-load with a 1 k&#937; test resistor.
...

Watch this Scientific Journal Video about A Simple Approach to Perform TEER Measurements Using a Self-Made Volt-Amperemeter with Programmable Output Frequency at JoVE.com

A Simple Approach to Perform TEER Measurements Using a Self-Made Volt-Amperemeter with Programmable Output Frequency

Here, we demonstrate how to set up an inexpensive volt-amperemeter with programmable output frequency that can be used with commercially available chopstick electrodes for transepithelial/endothelial electrical resistance measurements.

Transepithelial/endothelial electrical resistance (TEER) has been used since the 1980s to determine confluency and permeability of in vitro barrier model ...

Measurement of the transepithelial electrical impedance has been used since the 1980s to determine confluency and barrier function of epithelial monolayers in cell culture. The underlying technique is a four-terminal sensing which uses different pairs of current-carrying and voltage-sensing electrodes to make more accurate measurements. There are several commercially available devices to measure transepithelial impedance, but despite the ease of use and the high reliability, there are also some disadvantages as the non-translatable output frequency and their expensiveness.Thus, we represent how to build a cost-effective and programmable volt-ammeter. At first, we want to show how TEER measurement with commercially available devices works. To do so, we had cultured a cell layer of choroid plexus epithelial papilloma cells on Transwell filters with a pore size of three micrometer.This setting has been described by Schroten et al. as in vitro model of the blood-cerebrospinal fluid barrier. Now, a chopstick electrode is connected to an epithelial volt-ammeter.The device is switched on and set to measure resistance. The electrode is sterilized in 80%ethanol and subsequently equilibrated in an appropriate medium. The impedance to be measured will serve as reference value in order to evaluate the reliability of the volt-ammeter that will be assembled afterwards.In this example, we record an impedance of 680 ohms. Let's start with the assembly of a low-budget volt-ammeter with programmable output frequency. First of all, you will need a standard USB charger, and an USB extension cord as five-volt direct current power supply.An 8-bit microcontroller on a USB development board will then be used to generate a square wave current. Four cables with banana plugs are connected to two standard multimeters to measure voltage and current. Please ensure that the multimeters are capable of measuring current in a range of some microamperes with TrueRMS.A female RJ14 connector can be found on standard telephone cables. Just make sure, that the connector has six pins of which at least the inner four are wired. Finally, you will need some standard equipment, as our cables, a luster terminal, a 120 kiloohm resistor, and some tools as insulation strippers, a crimping tool, wire end ferrules, and soldering iron.The device is assembled exactly as illustrated in the layout diagram. At first, the USB extension is connected to the microcontroller. During normal operation, it is powered by a five-volt DC USB charger, that can readily be connected to a personal computer for programming.Two cables are stripped and crimped with wire end ferrules on one side. The other side is soldered either directly to pin zero and two of the microcontroller or to soldering lugs, which in turn are clipped on the respective pins. Next, the power-delivering cables are connected to a luster terminal.The first multimeter will be used to measure current and is connected in series with 120 kiloohm resistor and a current-passing chopstick electrodes. This arrangement ensures that the output current is limited, so the measurement will have no impact on cell viability. The four conductors of the telephone extension cord are dismantled and crimped to ferrules as shown before.Once the cable is prepared, you will have to test continuity of conductors and pins. In our example, pin three to six are connected to the white, brown, green and yellow conductor. Now pin five and six, that is green and yellow, are connected to the luster terminal to apply voltage to the outer electrode pair.Finally, you will have to connect the second multimeter, which will be used to measure the transepithelial voltage drop, to pins three and four, that is, in our example, to the white and brown conductor. We decided to mount installation in a cheap plastic chassis. Before the first use, the microcontroller has to be programmed.The source code is written in C+and can be uploaded by a USB. In brief, pin zero into a center output mode. When switched on, the function loop will start to alternate as pins between ground and plus five volts with a variable delay.In our example, we used a theoretical half-oscillation time of 40 milliseconds. Let's see how the measurement results compare to the reference values we had obtained before. The chopstick electrode is repositioned to the recently assembled volt-ammeter.The device is being powered on in three steps. That is, plugging in a USB charger, switching the left multimeter to AC voltage measurement, and switching the second multimeter to microampere. Pay attention, that alternating current has to be selected explicitly.In this example, the potential drop across the Transwell filter system is measured as approximately 25 millivolts, while we record a current of 37.1 microamperes. According to Ohm's Law, electric impedance can be easily calculated at 674 ohms, which is very close to the reference value of 680. We've shown that measurement values are reliable over a range from zero to 1.8 kiloohms.Thus, the described volt-ammeter can be used both for initial experiments and for further studies. However, if your results shall be published, you might always want to support your data, by measuring molecule flux across the respective cell layer.

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20.8K 조회수.  University of Tübingen. Measurement of the transepithelial electrical impedance has been used since the 1980s to determine confluency and barrier function of epithelial monolayers in cell culture. The underlying technique is a four-terminal sensing which uses different pairs of current-carrying and voltage-sensing electrodes to make more accurate measurements. There are several commercially available devices to measure transepithelial impedance, but despite the ease of use and the high reliability, there are also so...