Interface design for CMOS-integrated Electrochemical Impedance Spectroscopy (EIS) biosensors.
Ontology highlight
ABSTRACT:
SUBMITTER: Manickam A
PROVIDER: S-EPMC3522923 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:Tafel analysis and electrochemical impedance spectroscopy (EIS) have been widely used to characterize many kinds of electrocatalysts. The former provides the kinetic information of an electrochemical reaction with the exchange current while the latter does with the charge transfer resistance closely related to the exchange current. Both techniques, however, suffer from practical troubles which often decrease their reliabilities. In order to circumvent those troubles, an alternative was suggested that Tafel analysis was combined with EIS, even though its theoretical background was not clearly established. Tafel analysis is based on dc measurement, and EIS is on an ac one, respectively. Here, inspired by the second generation of EIS from chronoamperometry, we try to find how those techniques are correlated by investigating an amperometric response from EIS. The first step is Fourier transform of an arbitrary dc potential signal in the time domain to obtain the amplitudes and phases of the Fourier series which are equivalent to ac signals of each frequency. Second, with the Fourier series being applied onto the impedance data, the responding currents of each frequency are calculated by Ohm's law. Third, the current in the frequency domain is transferred back to the time domain by inverse Fourier transform to yield chronoamperometric or Tafel plots depending on the type of the applied dc potential. Finally, we can study Tafel plots based on EIS at different conditions and their correlations which are expected to be a better indicator for characterizing electrocatalysts instead of the slope of the classical Tafel analysis.
| S-EPMC6868906 | biostudies-literature
Project description:Here we provide a perspective concept of neurohybrid memristive chip based on the combination of living neural networks cultivated in microfluidic/microelectrode system, metal-oxide memristive devices or arrays integrated with mixed-signal CMOS layer to control the analog memristive circuits, process the decoded information, and arrange a feedback stimulation of biological culture as parts of a bidirectional neurointerface. Our main focus is on the state-of-the-art approaches for cultivation and spatial ordering of the network of dissociated hippocampal neuron cells, fabrication of a large-scale cross-bar array of memristive devices tailored using device engineering, resistive state programming, or non-linear dynamics, as well as hardware implementation of spiking neural networks (SNNs) based on the arrays of memristive devices and integrated CMOS electronics. The concept represents an example of a brain-on-chip system belonging to a more general class of memristive neurohybrid systems for a new-generation robotics, artificial intelligence, and personalized medicine, discussed in the framework of the proposed roadmap for the next decade period.
| S-EPMC7199501 | biostudies-literature
Project description:Ion-exchange membranes (IEMs) represent a key component in various electrochemical energy conversion and storage systems. In this study, electrochemical impedance spectroscopy (EIS) was used to investigate the effects of structural changes of anion exchange membranes (AEMs) on the bulk membrane and interface properties as a function of solution pH. The variations in the physico/electrochemical properties, including ion exchange capacity, swelling degree, fixed charge density, zeta potentials as well as membrane and interface resistances of two commercial AEMs and cation exchange membranes (CEMs, as a control) were systematically investigated in different pH environments. Structural changes of the membrane surface were analyzed by Fourier transform infrared and X-ray photoelectron spectroscopy. Most notably, at high pH (pH > 10), the membrane (Rm) and the diffusion boundary layer resistances (Rdbl) increased for the two AEMs, whereas the electrical double layer resistance decreased simultaneously. This increase in Rm and Rdbl was mainly attributed to the deprotonation of the tertiary amino groups (-NR2H+) as a membrane functionality. Our results show that the local pH at the membrane-solution interface plays a crucial role on membrane electrochemical properties in IEM transport processes, particularly for AEMs.
| S-EPMC8540937 | biostudies-literature
Project description:We propose monochromatic dark-field imaging microscopy (DFM) to measure the non-faradaic electrochemical impedance spectroscopy (EIS) of single Au nanorods (AuNRs). DFM was utilized to monitor the plasmonic scattering of monochromatic incident light by surface-immobilized individual AuNRs. When modulating the surface potential at a certain frequency, non-faradaic charging and discharging of AuNRs altered their electron density, leading to periodical fluctuations in the scattering intensity. Analysis of the amplitude and phase of the optical intensity fluctuation as a function of modulation frequency resulted in the EIS of single AuNRs. High-frequency (>100 Hz) modulation allowed us to differentiate the intrinsic charging effect from other contributions such as the periodic migration and accumulation of counterions in the surrounding medium, because the latter occurred at a longer timescale. As a result, single nanoparticle EIS led to the surface capacitance of single AuNRs being closer to the theoretical value. Since interfacial capacitance has been proven sensitive to molecular interactions, the present work also offers a new platform for single nanoparticle sensing by measuring the single nanoparticle capacitance.
| S-EPMC5956977 | biostudies-literature
Project description:Understanding the internal structure of composite nanofluids is critical for controlling their properties and engineering advanced composite nanofluid systems for various applications. This goal can be made possible by precise analysis with the help of a systematic robust platform. Here, we demonstrate a microfluidic device that can control the orientation of carbon nanomaterials in a suspension by applying external fields and subsequently examine the electrochemical properties of the fluids at microscale. Composite nanofluids were prepared using carbon nanomaterials, and their rheological, thermal, electrical, and morphological characteristics were examined. The analysis revealed that microfluidic electrochemical impedance spectroscopy (EIS) in the device offered more reliable in-depth information regarding the change in the microstructure of carbon composite nanofluids than typical bulk measurements. Equivalent circuit modelling was performed based on the EIS results. Furthermore, the hydrodynamics and electrostatics of the microfluidic platform were numerically investigated. We anticipate that this microfluidic approach can serve as a new strategy for designing and analyzing composite nanofluids more efficiently.
| S-EPMC5429664 | biostudies-literature
Project description:Despite advances in diagnosis and therapy, atherosclerotic cardiovascular disease remains the leading cause of morbidity and mortality in the Western world. Predicting metabolically active atherosclerotic lesions has remained an unmet clinical need. We hereby developed an electrochemical strategy to characterize the inflammatory states of high-risk atherosclerotic plaques. Using the concentric bipolar microelectrodes, we sought to demonstrate distinct Electrochemical Impedance Spectroscopic (EIS) measurements for unstable atherosclerotic plaques that harbored active lipids and inflammatory cells. Using equivalent circuits to simulate vessel impedance at the electrode-endoluminal tissue interface, we demonstrated specific electric elements to model working and counter electrode interfaces as well as the tissue impedance. Using explants of human coronary, carotid, and femoral arteries at various Stary stages of atherosclerotic lesions (n=15), we performed endoluminal EIS measurements (n=147) and validated with histology and immunohistochemistry. We computed the vascular tissue resistance using the equivalent circuit model and normalized the resistance to the lesion-free regions. Tissue resistance was significantly elevated in the oxLDL-rich thin-cap atheromas (1.57±0.40, n=14, p<0.001) and fatty streaks (1.36±0.28, n=33, p<0.001) as compared with lesion-free region (1.00±0.18, n=82) or oxLDL-absent fibrous atheromas (0.86±0.30, n=12). Tissue resistance was also elevated in the calcified core of fibrous atheroma (2.37±0.60, n=6, p<0.001). Despite presence of fibrous structures, tissue resistance between ox-LDL-absent fibroatheroma and the lesion-free regions was statistically insignificant (0.86±0.30, n=12, p>0.05). Hence, we demonstrate that the application of EIS strategy was sensitive to detect fibrous cap oxLDL-rich lesions and specific to distinguish oxLDL-absent fibroatheroma.
| S-EPMC3210389 | biostudies-literature
Project description:Plasmonic-based electrochemical impedance spectroscopy (P-EIS) is developed to investigate molecular binding on surfaces. Its basic principle relies on the sensitive dependence of surface plasmon resonance (SPR) signal on surface charge density, which is modulated by applying an ac potential to a SPR chip surface. The ac component of the SPR response gives the electrochemical impedance, and the dc component provides the conventional SPR detection. The plasmonic-based impedance measured over a range of frequency is in quantitative agreement with the conventional electrochemical impedance. Compared to the conventional SPR detection, P-EIS is sensitive to molecular binding taking place on the chip surface and less sensitive to bulk refractive index changes or nonspecific binding. Moreover, this new approach allows for simultaneous SPR and surface impedance analysis of molecular binding processes.
| S-EPMC3299414 | biostudies-literature
Project description:In the last decade, researchers have been searching for innovative platforms, methods, and techniques able to address recurring problems with the current cancer detection methods. Early disease detection, fast results, point-of-care sensing, and cost are among the most prevalent issues that need further exploration in this field. Herein, studies are focused on overcoming these problems by developing an electrochemical device able to detect telomerase as a cancer biomarker. Electrochemical platforms and techniques are more appealing for cancer detection, offering lower costs than the established cancer detection methods, high sensitivity inherent to the technique, rapid signal processing, and their capacity of being miniaturized. Therefore, Au interdigital electrodes and electrochemical impedance spectroscopy were used to detect telomerase activity in acute T cell leukemia. Different cancer cell concentrations were evaluated, and a detection limit of 1.9 × 105 cells/mL was obtained. X-ray photoelectron spectroscopy was used to characterize the telomerase substrate (TS) DNA probe self-assembled monolayer on gold electrode surfaces. Atomic force microscopy displayed three-dimensional images of the surface to establish a height difference of 9.0 nm between the bare electrode and TS-modified Au electrodes. The TS probe is rich in guanines, thus forming secondary structures known as G-quadruplex that can be triggered with a fluorescence probe. Confocal microscopy fluorescence images showed the formation of DNA G-quadruplex because of TS elongation by telomerase on the Au electrode surface. Moreover, electrodes exposed to telomerase containing 2',3'-dideoxyguanosine-5'-triphosphate (ddGTP) did not exhibit high fluorescence, as ddGTP is a telomerase inhibitor, thus making this device suitable for telomerase inhibitors capacity studies. The electrochemical method and Au microchip device may be developed as a biosensor for a point-of-care medical device.
| S-EPMC6796945 | biostudies-literature
Project description:Improving the performance of desalination membranes requires better measurements of salt permeability in the polyamide separating layer to elucidate the thermodynamic and kinetic components of membrane permselectivity. In this work, electrochemical impedance spectroscopy (EIS) is introduced as a technique to measure the salt permeability and estimate the salt partition coefficient in thin polyamide films created using molecular layer-by-layer deposition. The impedance of supported polyamide films ranging in thickness from 3.5 nm to 28.5 nm were measured in different electrolyte solutions. Impedance spectra were modeled with equivalent circuits containing resistive and capacitive elements associated with the EIS measurement system as well as characteristic low-frequency parallel resistive and capacitive elements that are associated with the polyamide film. The characteristic polyamide membrane resistance increases with film thickness, decreases with solution concentration, and is an order of magnitude greater for a divalent cationic solution than for a monovalent cationic solution. For each polyamide film, salt permeability is calculated from the membrane resistance, and a salt partition coefficient is estimated. At the highest solution concentration measured, which is representative of brackish water desalination conditions, the calculated salt permeabilities range from P s = 1.3 × 10-16 m s-1 to 3.9 × 10-16 m s-1, and the estimated salt partition coefficients range from K s = 0.008 to 0.016. These measurements demonstrate that EIS is a powerful tool for studying membrane permselectivity through the measurement of salt permeability in thin polyamide films.
| S-EPMC6774373 | biostudies-literature
Project description:Plaque rupture causes acute coronary syndromes and stroke. Intraplaque oxidized low density lipoprotein (oxLDL) is metabolically unstable and prone to induce rupture. We designed an intravascular ultrasound (IVUS)-guided electrochemical impedance spectroscopy (EIS) sensor to enhance the detection reproducibility of oxLDL-laden plaques. The flexible 2-point micro-electrode array for EIS was affixed to an inflatable balloon anchored onto a co-axial double layer catheter (outer diameter = 2 mm). The mechanically scanning-driven IVUS transducer (45 MHz) was deployed through the inner catheter (diameter = 1.3 mm) to the acoustic impedance matched-imaging window. Water filled the inner catheter to match acoustic impedance and air was pumped between the inner and outer catheters to inflate the balloon. The integrated EIS and IVUS sensor was deployed into the ex vivo aortas dissected from the fat-fed New Zealand White (NZW) rabbits (n=3 for fat-fed, n= 5 normal diet). IVUS imaging was able to guide the 2-point electrode to align with the plaque for EIS measurement upon balloon inflation. IVUS-guided EIS signal demonstrated reduced variability and increased reproducibility (p < 0.0001 for magnitude, p < 0.05 for phase at < 15 kHz) as compared to EIS sensor alone (p < 0.07 for impedance, p < 0.4 for phase at < 15 kHz). Thus, we enhanced topographic and EIS detection of oxLDL-laden plaques via a catheter-based integrated sensor design to enhance clinical assessment for unstable plaque.
| S-EPMC5068578 | biostudies-literature