- freely available
Micromachines 2014, 5(1), 1-12; doi:10.3390/mi5010001
Published: 7 January 2014
Abstract: In general, cell culture-based assays, investigations of cell number, viability, and metabolic activities during culture periods, are commonly performed to study the cellular responses under various culture conditions explored. Quantification of cell numbers can provide the information of cell proliferation. Cell viability study can understand the percentage of cell death under a specific tested substance. Monitoring of the metabolic activities is an important index for the study of cell physiology. Based on the development of microfluidic technology, microfluidic systems incorporated with impedance measurement technique, have been reported as a new analytical approach for cell culture-based assays. The aim of this article is to review recent developments on the impedance detection of cellular responses in micro/nano environment. These techniques provide an effective and efficient technique for cell culture-based assays.
Cell culture, which cultures cells as a monolayer on a surface of a cell culture vessel (e.g., Petri dish or multi-well microplate) is widely used in life science research for the investigation of cellular behavior. It has the advantage of simplicity in terms of operations and observations. In general cell culture-based assays, monitoring of cell number, viability, and metabolic activity are commonly performed to provide information of cellular responses under a specific culture condition studied. Conventionally, counting cells microscopically, quantifying indicative cellular components (e.g., DNA), live/dead fluorescent dye staining, and analysis of indicative metabolites synthesized by the cultured cells are adopted. These analytical methods have become standard protocols for the cell culture-based assays. However, these approaches are normally labor-intensive and time-consuming, limiting the throughput of the cell culture-based assay works like drug screening or toxin testing. In addition, analysis of the indicative cellular components and fluorescent dye staining normally need to sacrifice the cultured cells and thus hamper the observation of the subsequent cellular responses. Therefore, alternative analytical methods are crucial in need for achieving both effective and efficient detections.
In the past decade, microfluidic system, also called “lab-on-chip (LOC)”, “bio-chip”, or “micro-total-analysis-system (μTAS)”, has attracted attention because of its capability of combining engineering and life science [1,2,3]. Therefore, it is often interpreted as a miniaturized and automatic version of a conventional laboratory. Due to their miniaturization and automation, there are a number of advantages of using microfluidic systems, such as less sample/reagent consumption, reduced risk of contamination, less cost per analysis, lower power consumption, enhanced sensitivity and specificity, and higher reliability. Microfluidic systems have been developed for various biological analytical applications, such as DNA analysis [4,5,6,7,8], immunoassay [9,10,11,12,13], and cell analysis [14,15,16,17,18]. Moreover, a number of demonstrations showed that cell culture can be performed on the microfluidic systems to achieve higher throughput and more reliable results [19,20]. For example, a microfluidic device for culturing cells inside an array of microchambers with continuous perfusion of medium was reported to provide a cost-effective and automated cell culture . Each circular microchamber was 40 μm in height and surrounded by multiple narrow perfusion channels of 2 μm in height. The high aspect ratio between the microchamber and the perfusion channels offered a stable and homogenous microenvironment for cell growth. Human carcinoma (HeLa) cells were cultured in 10 × 10 microfluidic cell culture array and able to grow to confluency after eight days. Moreover, a fully automated cell culture screening system was developed and demonstrated on maintaining cell viability for weeks . Individual culture conditions in 96 independent culture chambers can be customized in terms of cell seeding density, composition of culture medium, and feeding schedule. Each chamber was imaged with time-lapse microscopy to perform quantitative measurements of the influence of transient stimulation schedules on cellular activities. In these excellent demonstrations, optical imaging was utilized to quantify cellular activities. However, this measurement technique is time-consuming and may induce large tolerance. Alternatively, impedance measurement was proposed to be one of the promising techniques to quantify cellular responses during culture on the microfluidic systems. The detection results are represented by electrical signals, which can easily interface with miniaturized devices. Typically, a pair of electrodes as an electrical transducer is utilized to measure the impedance change caused by the existence of the biological substances. Literature has demonstrated the use of the similar principle for the detection of various biological substances such as enzymes , antibodies and antigens [10,24,25,26], DNA [27,28], and cells [17,29,30,31,32,33]. This technique provides a non-invasive and label-free measurement, and is found practically useful for the detection of substances in miniaturized analytical devices like microfluidic systems.
The aim of this article is to review recent developments on the impedance detection of cellular responses in micro/nano environment. Cell number and cell viability are the important characteristics during cell culture, and can be monitored by various impedance measurement techniques. Moreover, as a microfluidic system is an integrated system for multi-purposes, monitoring of metabolic activities of cells with cell stimulation is also significant for cell culture-based studies. Literature review and in-depth discussion of the impedance measurement will be presented. Microfluidic systems incorporated with impedance measurement technique provide an effective and efficient technique for cell culture-based assays.
2. Electrical Equivalent Circuit
Generally, an electrical equivalent circuit is used to curve fit the experimental data for the explanation of the characteristics of the impedance detection system. A number of electrical equivalent circuits were proposed to describe the cellular detection . In order to have an easier understanding, a simplified electrical equivalent circuit and its impedance spectrum were reported and are shown in Figure 1 . It is generally suggested that two identical double layer capacitances at each electrode (Cdl) are connected to the medium resistance (Rsol) in series, and the dielectric capacitance of the medium (Cdi) is introduced in parallel with these series elements. In the equivalent circuit, there are two parallel branches, which are Cdi and Cdl + Rsol + Cdl. The impedance of each branch could be expressed with the following equations:
At a frequency below 1 MHz, the Cdi is inactive and is modeled as an open circuit. Current could not pass through the branch of dielectric capacitance and the total impedance is expressed as Z1. Both Cdl and Rsol are included in this frequency region, and they dominate at different frequencies, as shown in the impedance spectrum. At a low frequency range, the spectrum shows capacitive characteristics, which is contributed by the Cdl. The impedance decreases with increasing frequencies. Up to a certain frequency (depending on the electrode dimensions, and the conductivity and permittivity of the medium), the Cdl offer no impedance. The total impedance is contributed by the Rsol and is frequency-independent (resistive characteristics). When cells are present in the system, the presence of the electrically insulated cell membranes influences the Cdl as biological cells are very poor conductors at frequencies below 10 kHz . The conductivity of the cell membrane is around 10−7 S/m, whereas the conductivity of the interior of a cell can be as high as 1 S/m . Therefore, cell proliferation can be estimated by the total impedance at low frequency region.
3. Monitoring of Cell Number
3.1. Detection of Cells Adhered on the Electrode Surface
If cells adhere and proliferate on the surface of the measurement electrodes, the electrode surface area is effectively reduced and the total impedance across the electrodes is, hence, increased for the detection of the presence of cells. Most of the impedance biosensors are based on this principle. A pioneer work of cellular monitoring with an applied electric field was reported in 1984 . Later, impedance measurement of cell concentration, growth, and the physiological state of cells was demonstrated . An interdigitated electrode was utilized to demonstrate on-line and real-time cellular monitoring. Long-term cellular behavior was clearly shown by the impedance change of the electrodes. This detection principle was also applied to detect Salmonella typhimurium in mike samples . An interdigitated microelectrode was utilized as impedance sensors to measure the bacterial growth curve at four frequencies (10 Hz, 100 Hz, 1 kHz, and 10 kHz). Illustration of the experimental setup is shown in Figure 2. The most significant change in impedance was observed at 10 Hz. The biosensor can detect the bacterial concentration of 105–106 CFU/mL. Moreover, in order to detect cells specifically, antibodies are utilized to capture cells and provide selectivity to the sensor. Microelectrode array biosensors, with surface functionalization, were reported for the detection of Escherichia coli O157:H7  and Legionella pneumophila . The sensor surface was functionalized for bacterial detection using immobilized antibodies to create a biological sensing surface. The bacteria suspended in liquid samples were captured on the sensor surface and the impedance change was measured over a frequency range of 100 Hz–10 MHz. The sensors were able to determinate cellular concentrations of 104–107 CFU/mL and 105–108 CFU/mL, respectively. Another approach was to use magnetic nanoparticle-antibody conjugates (MNAC) to capture the specific cells. A microfluidic flow cell with embedded gold interdigitated array microelectrode was developed for rapid detection of Escherichia coli O157:H7 in ground beef samples . MNAC were used to separate and concentrate the target bacteria from the samples. The cells of E. coli O157:H7 inoculated in a food sample were first captured by the MNAC, separated and concentrated by applying a magnetic field, washed and suspended in solution, injected through the microfluidic flow cell, and attracted by magnetic field on the active layer for impedance measurement. This impedance biosensor was able to detect as low as 1.6 × 102 and 1.2 × 103 cells of E. coli O157:H7 cells present in pure culture and ground beef samples, respectively.
3.2. Detection of Suspended Cells
When cells suspend in the liquid buffer, impedance measurement can also be used to determine cell number in the buffer. However, the impedance spectroscopic responses are very dependent on the conductivity of the buffer used in the systems. The detection of Salmonella cell suspensions was demonstrated in deionzed (DI) water and phosphate buffered saline (PBS), respectively . It showed that bacterial cell suspensions in DI water with different concentrations can result in different electrical impedance spectral responses; conversely, cell suspensions in PBS cannot. The impedance spectra are shown in Figure 3. It was reported that the impedance of the cell suspensions in DI water decreased with the increasing cell concentration. It was suggested that the cell wall charges and the release of ions or other osmolytes from the cells caused the proportional impedance change.
4. Monitoring of Cellular Viability
Cell death leads to the release of cells from the surface of the measurement electrode. That induces the decrease of the impedance measured across the electrodes. Real-time evaluation of targeted tumor cells treated with a combination of targeted toxin and particular plant glycosides was demonstrated . HeLa cells were seeded onto interdigitated electrode and treated with targeted toxin. The impedance was directly correlated with the cell viability and able to trace the temporal changes of cell death during treatment. The above demonstration utilized a two-electrode system (i.e., interdigitated electrode) for the measurement. A three-electrode system was also demonstrated for the monitoring of cell growth with the treatment of potentially cytotoxic agents . It has the advantage of better reproducibility than traditional two-electrode impedance measurement. The cell chip consisted of an eight-well cell culture chamber incorporated with a three-electrode system on each well, as shown in Figure 4. Human hepatocellular carcinoma cells (HepG2) were cultured in the chamber and toxic effects on the HepG2 cells was monitored. The impedance was decreased after treatments with several toxicants, such as tamoxifen and menadione, indicating the detachment of dead cells. Moreover, a 10 × 10 micro-electrode array was used to monitor the culture behavior of mammalian cancer cells and evaluate the chemosensitivity of anti-cancer drugs using impedance spectroscopy . Human oesophageal cancer cells were cultured on the surface of the electrodes and then treated with anti-cancer drug. Morphology changes during cells adhesion, spreading, proliferation, and chemosensitivity effects on cells can be monitored by impedimetric analysis in a real-time and non-invasive way. Recently, commercial cell analyzers are available to monitor the cellular responses. Although they are not designed for microfluidic environment, but impedance measurement shows a promising tool for cellular analyses. Real-time detection of cell death in a neuronal cell line of immortalized hippocampal neurons (HT-22 cells), neuronal progenitor cells (NPC), and differentiated primary cortical neurons was demonstrated using the system . Schematic overview of the measurement principle is shown in Figure 5. These excellent demonstrations showed that impedance measurement is a convenient and reliable technique for real-time monitoring of cellular responses.
5. Monitoring of the Metabolic Activity of Cells
Monitoring of the metabolic activity during cell culture is very important for the study of cell physiology. A microfluidic chamber was reported to enable the real-time measurement of extracellular lactate of single heart cell under simultaneous electrical stimulation . This device is comprised of one pair of pacing microelectrodes, used for field-stimulation of the cell, and three other microelectrodes configured as an electrochemical lactate micro-biosensor. Single heart cell was stimulated at pre-determined rates and its metabolic conditions were explored under the "working" situation. Moreover, monitoring of cell medium by comparing the rates of glucose and oxygen before and after contact with cells was demonstrated . Two arrays of glucose and oxygen electrochemical sensors were fabricated at the inlet and outlet microchannels of the microfluidic cell culture chip, as shown in Figure 6. Real-time monitoring of glucose and oxygen was shown and the chip was utilized to the study of transient effluxes of these species during cell culture.
6. Cell Monitoring from 2D to 3D Cell Culture Format
Impedimetric cell monitoring in 2D cell culture format in microfluidic systems has been discussed and showed an effective and efficient technique for cell culture-based assays. 2D cell culture is widely adopted because of its simplicity in terms of operations and observations of cellular behavior. More recently, 3D culture format was proposed to provide a better approximation of the in vivo conditions in some cases [46,47]. Three-dimensional cell culture is that cells are encapsulated in a 3D polymeric scaffold material and can mimic the native cellular microenvironment since animal cells inhabit environments with very 3D features . Thus, that might provide a more physiologically meaningful culture condition for cell-based assays. However, since cells are encapsulated in the scaffold, direct observation of cellular behavior cannot be practically performed. Destructive methods, such as detection of indicative cellular components and fluorescent dye staining are commonly used for the cell analysis. Alternatively, impedance measurement technique was reported to provide a real-time and non-invasive way to monitor cellular response in the 3D scaffold . A microfluidic chip integrated with a pair of vertical electrodes in the 3D culture chamber was developed for quantifying cell number in the 3D scaffold. The impedance change was directly proportional to the cell number from 103 to 107 cells/mL in the 3D scaffold. This demonstration showed that the impedance measurement can be extended to monitor cellular responses from 2D to 3D cell culture format. It is expected that more demonstrations for real-time and non-invasive cellular monitoring will be reported.
With the rapid development of impedance measurement technique, commercial cell analyzers have been launched recently to provide convenient and reliable equipment for life science research and pharmaceutical development. In this article, impedance detection of cellular response in micro/nano environment has been discussed. The microfluidic systems incorporated with impedance measurement technique provide non-invasive and label-free monitoring of cellular responses in 2D and 3D culture format. More importantly, these systems are miniaturized and automatic. A sterile and homogenous microenvironment for cell culture can be created for precise monitoring. It is believed that more cell culture-based assays will be reported using the microfluidic cell culture systems.
Author would like to thank the National Science Council, Taiwan for the financial support (project no. NSC101-2221-E-182-003-MY3).
Conflicts of Interest
The author declares no conflict of interest.
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