Search Results (410)

Prostate cancer is among the most prevalent malignancies in men worldwide, underscoring the need for early and accurate diagnostic tools. This study presents a proof-of-concept and pilot clinical validation of a novel bioelectric impedance-based biosensor for the detection of prostate-specific antigen (PSA) in human serum. The system integrates Molecular Identification through Membrane Engineering (MIME) with the xCELLigence real-time cell analysis platform, employing Vero cells electroinserted with anti-PSA antibodies. Optimization experiments identified 15,000 cells/well as the optimal configuration for impedance response. The biosensor exhibited specific, concentration-dependent changes in impedance upon exposure to PSA standard solutions and demonstrated significant differentiation between PSA-positive and PSA-negative human serum samples relative to the clinical threshold of 4 ng/mL. The biosensor offered rapid results within one minute, unlike standard immunoradiometric assay (IRMA), while showing strong diagnostic agreement. The system’s specificity, sensitivity, and reproducibility support its potential for integration into point-of-care screening workflows. This bioelectric assay represents one of the fastest PSA detection approaches reported to date and offers a promising solution for reducing overdiagnosis while improving clinical decision-making and patient outcomes. Full article

The escalating threat of infectious diseases necessitates the development of diagnostic technologies that are not only rapid and sensitive but also deployable at the point of care. Electrochemical impedance spectroscopy (EIS) has emerged as a leading technique for the label-free detection of pathogens, offering a unique combination of sensitivity, non-invasiveness, and adaptability. This review provides a comprehensive overview of the design and application of EIS-based biosensors tailored for pathogen detection, focusing on critical components such as biorecognition elements, electrode materials, nanomaterial integration, and surface immobilization strategies. Special emphasis is placed on the mechanisms of signal generation under Faradaic and non-Faradaic modes and how these underpin performance characteristics such as the limit of detection, specificity, and response time. The application spectrum spans bacterial, viral, fungal, and parasitic pathogens, with case studies highlighting detection in complex matrices such as blood, saliva, food, and environmental water. Furthermore, integration with microfluidics and point-of-care systems is explored as a pathway toward real-world deployment. Emerging strategies for multiplexed detection and the utilization of novel nanomaterials underscore the dynamic evolution of the field. Key challenges—including non-specific binding, matrix effects, the inherently low ΔR_ct/decade sensitivity of impedance transduction, and long-term stability—are critically evaluated alongside recent breakthroughs. This synthesis aims to support the future development of robust, scalable, and user-friendly EIS-based pathogen biosensors with the potential to transform diagnostics across healthcare, food safety, and environmental monitoring. Full article

We develop a modular, wireless, solar- and battery-powered system for detecting chlorpyrifos (Lorsban^TM 2.5% DP) in water using electrochemical impedance spectroscopy (EIS). The system integrates a Raspberry Pi Zero 2W for data processing, Python-based software (version 3.12.2), and a solar charge manager to power all components via a lithium-ion battery and solar panel. A commercial EmStat Pico Module and an amperometric biosensor with acetylcholinesterase (AChE) detect chlorpyrifos. Nine water samples with varying concentrations were tested using a 20 Hz–200 kHz frequency sweep and 15 mV excitation. Bode plots and statistical analyses confirmed statistically significant impedance variation as a function of chlorpyrifos concentration, validating the system as a portable, sensitive, and effective tool for environmental monitoring. Full article

Sepsis remains a global health emergency, demanding timely and accurate diagnostics to reduce morbidity and mortality. This review critically assesses the recent progress (2020–2025) in the development of electrochemical aptamer-based biosensors for sepsis detection. These biosensors combine aptamers’ high specificity and modifiability with the sensitivity and miniaturization potential of electrochemical platforms. The analysis highlights notable advances in detecting key sepsis biomarkers, such as C-reactive protein (CRP), procalcitonin (PCT), interleukins (e.g., interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α)), lipopolysaccharides (LPSs), and microRNAs using diverse sensor configurations, including a field-effect transistor (FET), impedance spectroscopy, voltammetry, and hybrid nanomaterial-based systems. A comparative evaluation reveals promising analytical performance in terms of the limit of detection (LOD), rapid response time, and point-of-care (POC) potential. However, critical limitations remain, including variability in validation protocols, limited testing in real clinical matrices, and challenges in achieving multiplexed detection. This review underscores translational barriers and recommends future directions focused on clinical validation, integration with portable diagnostics, and interdisciplinary collaboration. By consolidating current developments and gaps, this work provides a foundation for guiding next-generation biosensor innovations aimed at effective sepsis diagnosis and monitoring. Full article

The electrochemical impedance spectroscopy (EIS) is a measurement method for characterizing bio-recognition events of a sensor, such as field-effect transistor-based biosensors (BioFETs). Due to the lack of portable impedance spectroscopes, EIS applies mainly in laboratories preventing application-oriented use in the field. This work presents a portable impedance analyzer (PIA) providing a 4-channel EIS of BioFETs. It performs the analysis of the recorded spectra by determining the charge transfer resistance ${\mathrm{R}}_{\mathrm{ct}}$ with a power-saving algorithm. Therefore, a circle is fitted into the Nyquist representation of the Randles circuit, from whose zero crossings ${\mathrm{R}}_{\mathrm{ct}}$ can be determined. The introduced algorithm was evaluated on 100 simulated spectra of Randles circuits. To analyze the overall system, an adjustable reference circuit was developed that simulates configurable Randles circuits. Additional measurements with pH-sensitive ion-sensitive field-effect transistors (ISFETs) demonstrate the application of the measurement system with electrochemical sensors. Using simulated spectra, the circular fitting is able to detect ${\mathrm{R}}_{\mathrm{ct}}$ with a median accuracy of $1.2\%$ at an average nominal power of 40 mW and 3054 µs computing time. The PIA with the embedded implementation of the circuit fitting achieves a median error for R_ct of 4.2% using the introduced Randles circuit simulator (RCS). Measurements with ISFETs show deviations of 6.5 ± 2.8% compared to the complex non-linear least squares (CNLS), but is significantly faster and more efficient. The presented system allows a portable, power-saving performance of EIS. Future optimizations for a specific applications can improve the presented system and enable novel low-power and automated measurements of biosensors outside the laboratory. Full article

Cortisol is a key biomarker for stress detection, and its levels can be monitored using point-of-care devices with sensors such as nanoparticles and interdigitated array electrodes (IDEs). This study developed an IDE platform using barium titanate (BaTiO₃) particles synthesized via colloidal precipitation with titanium tetraisopropoxide, barium chloride, and Pluronic^® P123. The calcination temperatures varied between 160 °C and 340 °C, with optimal results observed at 160 °C. Scanning electron microscopy revealed particles with an average size of 26 nm, and Fourier transform infrared spectroscopy confirmed the molecular composition after the removal of P123. X-ray diffraction analysis revealed anatase and brookite phases. Brunauer-Emmett-Teller analysis indicated changes in pore morphology, with samples treated at 160 °C exhibiting a type IV(a) mesoporous structure, a surface area of 163 m²/g, and an average pore diameter of 5.24 nm. Higher temperatures led to transitions to type IV(b) at 260 °C and type V at 340 °C, with reduced pore size. Electrochemical impedance spectroscopy was employed to evaluate the performance of the IDE sensor integrated with BaTiO₃ nanoparticles and albumin across cortisol concentrations ranging from 5.0 to 20 ng/mL. Impedance measurements revealed a significant decrease in impedance (Z′) with increasing cortisol concentrations, indicating increased conductivity. Specifically, Nyquist plots for a saliva sample containing 5 ng/mL cortisol—within the typical physiological range—exhibited a marked increase in charge-transfer resistance (Rct), confirming the sensor’s ability to detect low hormone levels in biological fluids. These findings underscore the potential of BaTiO₃-based IDE platforms at 160 °C for stress biomarker monitoring. Full article

The world urgently needs new methods to quickly and efficiently detect mutated viruses. An RNA-AuNP-based colorimetric biosensor is a highly sensitive, specific, and cost-effective tool that enables rapid, visual detection of target molecules for applications in disease diagnostics, environmental monitoring, and forensic analysis. An RNA-AuNP-based colorimetric biosensor requires precise control over nanoparticle dispersion and aggregation, which can be achieved using temperature regulation. A novel on-chip microelectrode is proposed to induce and monitor the aggregation of RNA-attached gold nanoparticles (AuNPs) through Joule heating and impedance spectroscopy. The proposed platform is implemented based on printed circuit board (PCB) technology, which has many advantages, such as fast and easy design and fabrication, low power consumption, and low costs. Joule heating is the process in which the energy of an electric current is converted into heat as it flows through a resistance. Impedance spectroscopy is an analytical technique that measures a system’s electrical response to an applied AC signal across a range of frequencies, providing insights into a sample’s dielectric properties. The results validate that the fabricated microelectrode is capable of heating a 20 µL droplet to 75 °C within 30 s, utilizing a low power input of only 3.75 watts and successfully inducing a color change based on the presence of hepatitis C virus (HCV) RNA, while impedance readings are used to monitor the aggregation. Full article

A user-friendly, portable, low-cost readout system for the on-site or point-of-care characterization of chemo- and biosensors based on an electrolyte–insulator–semiconductor capacitor (EISCAP) has been developed using a thumb-drive-sized commercial impedance analyzer. The system is controlled by a custom Python script and allows to characterize EISCAP sensors with different methods (impedance spectra, capacitance-voltage, and constant-capacitance modes), which are selected in a user interface. The performance of the portable readout system was evaluated by pH measurements and the detection of the antibiotic penicillin, hereby using EISCAPs consisting of Al/p-Si/SiO₂/Ta₂O₅ structures and compared to the results obtained with a stationary commercial impedance analyzer. Both the portable and the commercial systems provide very similar results with almost perfectly overlapping recorded EISCAP signals. The new portable system can accelerate the transition of EISCAP sensors from research laboratories to commercial end-user devices. Full article

This paper introduces a novel-shaped, compact, multiband monopole antenna sensor incorporating an irregular curved split-ring resonator (SRR) design for non-invasive, continuous monitoring of human blood glucose levels (BGL). The sensor operates at multiple resonance frequencies: 0.94, 1.5, 3, 4.6, and 6.3 GHz, achieving coefficient reflection impedance bandwidths ≤ −10 dB of 4%, 1%, 3.5%, 65%, and 50%, respectively. Additionally, novel shapes of two SRR metamaterial cells create notches at 1.7 GHz and 4.4 GHz. The antenna is fabricated on an economical FR4 substrate with compact dimensions of 35 × 50 × 1.6 mm³. The sensor’s performance is evaluated using 3D electromagnetic software, incorporating a human finger phantom model and applying the Cole–Cole model to mimic the blood layer’s sensitivity to blood glucose variations. The phantom model is positioned at different angles relative to the biosensor to detect frequency shifts corresponding to different glucose levels. Experimental validation involves placing a real human finger around the sensor to measure resonant frequency, magnitude, and phase changes. The fabricated sensor demonstrates a superior sensitivity of 24 MHz/mg/dL effectiveness compared to existing methods. This emphasizes its potential for practical, non-invasive glucose monitoring applications. Full article

Disease diagnosis is not only related to individual health but is also a crucial part of public health prevention. Electrochemical biosensors combine the high sensitivity of electrochemical methods with the inherent high selectivity of biological components, offering advantages such as excellent sensitivity, fast response time, and low cost. The generated electrical signals have a linear relationship with the target analyte, allowing for identification and concentration detection. This has become a very attractive technology. This review offers a summary of recent advancements in electrochemical biosensor research for disease diagnosis in China. It systematically categorizes and summarizes biosensors developed in China for detecting cancer, infectious diseases, inflammation, and neurodegenerative disorders. Additionally, the review delves into the fundamental working principles, classifications, materials, preparation techniques, and other critical aspects of electrochemical biosensors. Finally, it addresses the key challenges impeding the advancement of electrochemical biosensors in China and examines promising future directions for their development. Full article

Surface-imprinted polymers (SIPs) represent an exciting and cost-effective alternative to antibodies for electrochemical impedance spectroscopy (EIS)-based biosensing. They can be produced using simple printing techniques and have shown high efficacy in detecting large biomolecules and microorganisms. Stamp imprinting, a novel SIP method, creates the target analyte’s imprint using a soft lithography mask of the analyte matrix, thereby reducing material complexities and eliminating the need for cross-linking, which makes the process more scalable than the conventional SIPs. In this work, we demonstrate a stamp-imprinted EIS biosensor using a biocompatible polymer, polycaprolactone (PCL), for quantifying amyloid beta-42 (Aβ-42), a small peptide involved in the pathophysiology of Alzheimer’s disease. The evaluated SIP-EIS biosensors showed a detection limit close to 10 fg/mL, and a detection range covering the physiologically relevant concentration range of the analyte in blood serum (from 10 fg/mL to 10 μg/mL). The device sensitivity, which is found to be comparable to antibody-based EIS devices, demonstrates the potential of SIP-EIS biosensors as an exciting alternative to conventional antibody-based diagnostic approaches. We also evaluate the viability of analyzing these proteins in complex media, notably in the presence of serum albumin proteins, which cause biofouling and non-specific interactions. The combination of high sensitivity, selectivity, and ease of fabrication makes SIP-EIS biosensors particularly suited for portable and point-of-care applications. Full article

Interleukin-8 (IL-8) is a critical biomarker associated with inflammation and disability in both adults and newborns. Conventional detection methods are often labor-intensive, time-consuming, and require highly trained personnel. Non-Faradaic impedimetric biosensors offer a label-free, rapid, and direct approach for IL-8 detection. While previous studies have primarily focused on capacitance and phase changes, the potential of other impedimetric parameters remains underexplored. In this study, a gold interdigitated electrode (Au-IDE)-based non-Faradaic biosensor was developed for IL-8 detection, evaluating multiple impedimetric parameters, including capacitance, impedance magnitude (Z_mod), real impedance (Z_real), and imaginary impedance (Z_imag). Among these, Z_imag exhibited the lowest limit of detection (LoD) at 90 pg/mL, followed by Z_mod at 120 pg/mL, and capacitance at 140 pg/mL, all significantly below the clinical threshold of 600 pg/mL. In contrast, Z_real displayed the highest LoD at 1.3 ng/mL. Sensitivity analysis revealed that Z_imag provided the highest sensitivity at 13.1 kΩ/log (ng/mL), making it the most effective parameter for detecting IL-8 at low concentrations. The sensitivity of Z_mod and Z_real was lower, while capacitance sensitivity was measured at 20 nF/log (ng/mL). These findings highlight the importance of investigating alternative impedimetric parameters beyond capacitance to optimize biosensor performance for biomarker detection. This study demonstrates that non-Faradaic biosensors, despite their capacitive-based nature, can achieve enhanced sensitivity and detection limits by leveraging additional impedimetric parameters, offering a promising approach for rapid and effective IL-8 detection. Full article

Biomolecular detection plays essential and irreplaceable roles in safeguarding human health, impeding the transmission of diseases, and augmenting the efficacy of treatments. The precise and specific identification of biomarkers holds profound significance for the early diagnosis, real-time surveillance, and targeted treatment of various diseases. In the initial phases of numerous diseases, the absence of distinct biomarkers in the bloodstream often leads to weak detection signals when using traditional immune detection methods such as enzyme-linked immunosorbent assays (ELISAs), chemiluminescence, and fluorescence chromatography. With the surge in research on surface plasmons, innovative approaches have recently emerged that combine surface plasmon resonance (SPR) with immunological detection techniques, reducing the detection sensitivity to 283 ag/mL, shrinking the sensor size to 2.228 µm², and shortening the detection time to 5.5 min. This review provides an overview of the theoretical foundations of surface plasmon resonance and immunoassays and then delves into the latest advancements in biosensors based on these principles, categorizing them according to their detection mechanisms and methodologies. Finally, we discuss future research directions, opportunities, and the challenges hindering the development of highly sensitive immuno-biochips. Full article

The global market increasingly demands alternative rapid diagnostic tools, such as disposable biosensors, to meet the growing need for point-of-care clinical testing of infectious diseases. Bacterial vaginosis (BV), a common infection caused by Gardnerella vaginalis, requires efficient and accurate detection methods to improve patient outcomes and prevent complications. However, existing diagnostic approaches often lack sensitivity, specificity, or rapid response times, highlighting the need for innovative biosensing solutions. In response to this challenge, we developed a peptide-based electrochemical biosensor for the specific detection of Gardnerella vaginalis. The sensor was designed to achieve high sensitivity, selectivity, and stability, with detection performed through electrochemical techniques. Cyclic voltammetry (CV) was employed to monitor electron transfer kinetics at the electrode surface, while electrochemical impedance spectroscopy (EIS) provided insights into changes in resistance and capacitance during peptide binding. The sensor fabrication involved covalently bonding anti-Gardnerella vaginalis peptides to a gold nanoparticle (AuNP)-modified graphene electrode, significantly enhancing bioreceptor immobilization stability and increasing the surface area for target binding interactions. The incorporation of AuNPs improved signal amplification due to their high surface-to-volume ratio and excellent conductivity, leading to enhanced sensor performance. The biosensor demonstrated a low detection limit (LOD) of 0.02305 μg/mL, with a rapid response time of 5 min across various concentrations of the target Gardnerella vaginalis antigen. The results confirmed specific and selective binding to the pathogen marker, with minimal interference from non-target species, ensuring high accuracy. The combination of graphene, AuNPs, and peptide bioreceptors resulted in robust signal enhancement, making this biosensor a promising tool for fast and reliable point-of-care diagnostics in clinical settings. Full article

Biosensors as advanced analytical tools have found various applications in food safety, healthcare, and environmental monitoring in rapid and specific detection of target analytes in small liquid samples. Up to now, planar electrochemical electrodes have shown the highest potential for biosensor applications due to their simple and compact construction and cost-effectiveness. Although a number of commercially available electrodes, manufactured from various materials on different substrates, can be found on the market, their high costs for single use and low reproducibility persist as major drawbacks. In this study, we present an innovative, cost-effective approach for the rapid fabrication of electrodes that combines lamination of 24-karat gold leaves with low-cost polyvinyl chloride adhesive sheets followed by laser ablation. Laser ablation enables the creation of electrodes with customizable geometries and patterns with microlevel resolutions. The developed electrodes are characterized by cyclic voltammetry and electrochemical impedance spectroscopy, scanning electronic microscopy, and 3D profiling. To demonstrate the manufacturing and biosensing potential, different geometries and shapes of electrodes were realized as the electrochemical transducing platform and applied for the realization of magnetic bead (MB)-labeled biosensors for quantitative detection of food-borne pathogens of Salmonella typhimurium (S. typhimurium) and Listeria monocytogenes (L. monocytogenes). Full article