Theoretical treatment and computer simulation of microelectrode arrays

High-sensitivity electrochemical enzyme-linked assay on a microfluidic interdigitated microelectrode

Neuronal differentiation and synapse formation of PC12 and embryonic stem cells on interdigitated microelectrode arrays:: Contact structures for neuron-to-electrode signal transmission (NEST)

Electrochemically activated carbon micro-electrode arrays for electrochemical micro-capacitors

A small-volume voltammetric detection of 4-aminophenol (PAP) has been developed using an interdigitated array (IDA) microelectrode cell in order to apply the IDA to electrochemical enzyme immunoassay. The signal of PAP at the IDA was steady state, and its magnitude was amplified compared with that of the usual single electrode due to redox cycling of PAP between the two finger sets of the IDA. A linear relationship between PAP concentration and cathodic limiting current was obtained from 1 to 1000 microM, reproducibly. The minimum sample volume in the measurement was reduced to 800 nL. High sample throughput of less than 1-min detection time per sample was achieved on 2-10-microL PAP samples. This IDA cell was applied to the electrochemical enzyme immunoassay of mouse IgG. Alkaline phosphatase was used as the enzyme label. The mouse IgG concentration was evaluated by detecting the concentration of PAP, which is the product of enzymatic reaction of the substrate, 4-aminophenyl phosphate (PAPP). Anti-mouse IgG was covalently immobilized on the glass surface of the small-volume immunowells by carbodiimide coupling. The assay range was 10-1000 ng/mL using 10-microL sample and 20-microL substrate solutions.

A 3D dendritic nanostructure of silver‐array (DSA) was prepared via electrodeposition on an interdigitated array (IDA) microelectrode. For preparation of this nanostructure, the optimal parameters such as deposition potential, deposition time, the electrode bandwidth and gap size were systematically investigated. It was found that the edge effect of the IDA microelectrode is a key factor for controlling the 3D dendritic growth of silver. Furthermore, the formation of the 3D dendritic morphology was discussed from the aspect of electrochemical nucleation theory and nonequilibrium growth dynamics to give a deep understanding of its growth mechanism. For its potential practical application, we showed that the as‐prepared 3D DSA nanomaterial exhibited high electrocatalytic reduction ability to nitrate in neutral solution and excellent performance for nitrate determination. An amperometric nitrate microsensor based on the 3D DSA was obtained.

An interdigitated microelectrode array (IDA) biamperometric titration is presented for the microdetermination of formaldehyde. It is based on a direct titration of formaldehyde with hydroxylamine under the formation of formaldoxime. The released hydrogen cations react with hydroxyl anions in 0.1 M NaOH. The interdigitated pair of two individually polarizable microelectrodes serves as a biamperometric end-point indicator. Hydroxylamine together with dissolved free oxygen behave as a quasi reversible mixed redox system, therefore a significant increase of current flowing between the IDA segments polarized by 100 mV is observed when the first excess of titrant appears in the titrated solution. Because of the small dimension of the IDA sensor this principle can be extended for a microanalytical variant of this method. Formaldehyde contents down to 10−3 M in small volume waste water samples could be determined by this technique. These samples usually contain carboxylic acids which interfere in iodimetric determinations, but do not influence the titration of formaldehyde with hydroxylamine.

A microfluidic flow cell with embedded gold interdigitated array microelectrode (IDAM) was developed and integrated with magnetic nanoparticle-antibody conjugates (MNAC) into an impedance biosensor to rapidly detect pathogenic bacteria in ground beef samples. The flow cell consisting of a detection microchamber and inlet and outlet microchannels was fabricated by bonding an IDAM chip to a poly(dimethylsiloxane) (PDMS) microchannel. The detection microchamber with a dimension of 6 mm × 0.5 mm × 0.02 mm and a volume of 60 nL was used to collect bacterial cells in the active layer above the microelectrode for sensitive impedance change. MNAC were prepared by conjugating streptavidin-coated magnetic nanoparticles with biotin-labeled polyclonal goat anti-E. coli antibodies and were used in the separation and concentration of target bacteria. 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 then suspended in mannitol solution and finally injected through the microfluidic flow cell 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 sample, respectively. The total detection time from sampling to measurement was 35 min. Equivalent circuit analysis indicated that the bulk medium resistance, double layer capacitance, and dielectric capacitance were responsible for the impedance change due to the presence of E. coli O157:H7 cells on the surface of IDAM. Sample pre-enrichment, secondary antibodies on the microelectrode surface, and redox probes were not required in this impedance biosensor.

Electrogenerated chemiluminescence (ECL) from a solution of ruthenium (II) tris(2,2'-bipyridyl) Ru(bpy)/sub 3//sup 2+/ generated at an interdigitated microelectrode array (IDA) and detected with an on-chip integrated silicon photodiode is reported. This novel approach combines the analytical properties of IDAs with the high sensitivity and selectivity of ECL reactions, together with the convenience in using an integrated photometric device.

This paper reports the design, fabrication and testing of a microchip wherein interdigitated microelectrode arrays (IMEA) were integrated with bipolar semiconductor photodiode array (PDA) chip to fabricate a highly compact embodiment for on-chip handling of solutions and electrochemiluminescence (ECL) detection. A 12 x 12 micro array of photodiodes, each coupled with an interdigitated microelectrode array (IMEA), an array of current amplifiers, and a photodiode element-addressing circuit were integrated into a single 2 x 2 cm² IC chip. Each photodiode had dimensions of 300 x 300 μm² and the photodiode-to-photodiode distance was 100 μm. The chip was successfully applied to the on-chip quantification of electro-chemiluminescing probe-labeled single stranded oligonucleotides. The minimum detectable limit at signal/noise ≥ 3 was found to be 5 x 10⁻¹⁴ moles of oligonucleotides with a sample volume as low as 5 microl (i.e., 10 fmole/μl). The attractive features of the developed IMEA-PDA microchip are that a plurality of samples can be analyzed simultaneously using a chip and that for a given sample the data can be averaged from values obtained from multiple, individually addressed pixels. These in turn bring in speed and statistical confidence in analysis. The IMEA-PDA microchip system has the potential to be used as a versatile and highly compact chemical analysis tool for chemical sensing and metrology applications.

Shewanella oneidensis MR-1 can gain energy by performing extracellular electron transport (EET) to external insoluble electron acceptors ranging from natural minerals to synthetic electrode surfaces when poised at proper potentials. Outer membrane c-type multi-heme cytochromes play a critical role in mediating this electron transport. The abundance of these cytochromes on the cell surface has also been hypothesized to facilitate long-distance electron transport along multicellular biofilms, in a manner similar to redox active polymers containing discrete redox moieties. Here we report measurements of electron transport in living S. oneidensis biofilms that bridged interdigitated array (IDA) microelectrodes. Electrochemical gating reveals a peak in the conduction current at the expected formal potential of the cytochrome conduits, consistent with redox conductivity where transport is driven by a multistep electron hopping mechanism through the heme network. The temperature dependency of the biofilm conduction is also consistent with such a thermally activated process, where conductivity increases with increasing temperature. In addition, the measured activation energy (0.315 eV) is consistent with the computationally-determined activation energy of the S. oneidensis Mtr decaheme cytochromes.

The organic electrochemical transistors (OECTs) are largely applied as bio‐ and ion‐sensor devices due to their performance in an aqueous environment with electrochemical doping/dedoping (reversible redox reactions) of the semiconducting layer through ion injection and also low (around 1 V) operation potentials. Aiming for the complementary circuits’ development and improvement of the sensors device, we report the application of spin coated polyaniline (PANI) in ambipolar OECT. The OECT operation is based on electrochemical protonation/deprotonation of PANI upon applied gate potential that was verified by cyclic voltammograms (CV) of PANI sample. The device operates in accumulation mode with on‐currents on the milliampere range due to the use of interdigitated array (IDA) microelectrodes architecture with a larger active area. Acid (HCl) doped PANI were applied in OECT device for comparison, and it presented improved performance with increasing drain‐source current up to 38%, reaching 4.8 mA for the n‐type device. This current increase is due to the narrower bandgap of doped PANI that affects the injection barrier. The HCl doped PANI was evaluated by UV‐Vis spectrophotometry and CV analysis. Using deionized water as electrolyte defunctionalized the PANI‐based OECT (no current modulation observed) because the absence of ions in the electrolyte interrupts the electrochemical doping. This is the opposite for the poly(3‐hexylthiophene) (P3HT)‐based electrolyte‐gated organic field‐effect transistor (EGOFET) due to the polymeric hydrophobicity nature that allows for field‐effect modulation in the electrolyte/semiconductor interface. The results presented may open new possibilities for bio‐ and ion‐sensors devices.

3D microelectrode arrays, pushing the bounds of sensitivity toward a generic platform for point-of-care diagnostics

Geobacter spp. can acquire energy by coupling intracellular oxidation of organic matter with extracellular electron transfer to an anode (an electrode poised at a metabolically oxidizing potential), forming a biofilm extending many cell lengths away from the anode surface. It has been proposed that long-range electron transport in such biofilms occurs through a network of bound redox cofactors, thought to involve extracellular matrix c-type cytochromes, as occurs for polymers containing discrete redox moieties. Here, we report measurements of electron transport in actively respiring Geobacter sulfurreducens wild type biofilms using interdigitated microelectrode arrays. Measurements when one electrode is used as an anode and the other electrode is used to monitor redox status of the biofilm 15 μm away indicate the presence of an intrabiofilm redox gradient, in which the concentration of electrons residing within the proposed redox cofactor network is higher farther from the anode surface. The magnitude of the redox gradient seems to correlate with current, which is consistent with electron transport from cells in the biofilm to the anode, where electrons effectively diffuse from areas of high to low concentration, hopping between redox cofactors. Comparison with gate measurements, when one electrode is used as an electron source and the other electrode is used as an electron drain, suggests that there are multiple types of redox cofactors in Geobacter biofilms spanning a range in oxidation potential that can engage in electron transport. The majority of these redox cofactors, however, seem to have oxidation potentials too negative to be involved in electron transport when acetate is the electron source.

Selective detection of specific bacteria using dielectrophoretic impedance measurement method combined with an antigen–antibody reaction

The requirement for on-line and in-situ monitoring of analytes in process and effluent streams and in ground waters has become increasingly more important in recent years. We therefore describe the development of the transduction element for a fully automated online instrument for the detection of caesium. The sensor layer for this instrument employs an Ion Selective Conductimetric microsensor (ISCOM) as the detector. This is based upon a plasticized polymeric membrane incorporating a selective ionophore, overlaying two interdigitated microelectrode arrays. A direct relationship has been observed between the bulk conductance (as determined by the microelectrodes) of the ionophore loaded membrane and the concentration of the primary ions in solution. Caesium selective ISCOMs were prepared using a ion selective membrane containing the commercially available ionophore Calix[6]arene-hexaacetic acid hexaethyl ester, polyvinylchloride (PVC) and plasticiser Nitrophenylether (NPOE). Methods of ion selective membrane deposition have been investigated in order to obtain a maximal response. The relative levels of membrane components have also been varied in order to further enhance the ISCOM reponse. We also present preliminary data concerning the caesium selectivity with respect to a range of possible interferents, including rubidium.