Electrochemical Detection Method Research Articles

Ultrasensitive and Rapid Circulating Tumor DNA Liquid Biopsy Using Surface-Confined Gene Amplification on Dispersible Magnetic Nano-Electrodes.

Circulating tumor DNA (ctDNA) detection has been acknowledged as a promising liquid biopsy approach for cancer diagnosis, with various ctDNA assays used for early detection and treatment monitoring. Dispersible magnetic nanoparticle-based electrochemical detection methods have been proposed as promising candidates for ctDNA detection based on the detection performance and features of the platform material. This study proposes a nanoparticle surface-localized genetic amplification approach by integrating Fe3O4-Au core-shell nanoparticles into polymerase chain reactions (PCR). These highly dispersible and magnetically responsive superparamagnetic nanoparticles act as nano-electrodes that amplify and accumulate target ctDNA in situ on the nanoparticle surface upon PCR amplification. These nanoparticles are subsequently captured and subjected to repetitive electrochemical measurements to induce reconfiguration-mediated signal amplification for ultrasensitive (∼3 aM) and rapid (∼7 min) metastatic breast cancer ctDNA detection in vitro. The detection platform can also detect metastatic biomarkers from in vivo samples, highlighting the potential for clinical applications and further expansion to rapid and ultrasensitive multiplex detection of various cancers.

Dual-Mode Virus Detection: Combining Electrochemical and Fluorescence Modalities for Enhanced Sensitivity and Reliability.

This study introduces a dual-mode biosensor specifically designed for the quantitative detection of viruses in rapid analysis. The biosensor is unique in its use of both optical (fluorescence) and electrochemical (impedance) detection methods using the same nanocomposites, providing a dual confirmation system for virus (norovirus-like particles) quantification. The system is based on using two antibody-conjugated nanocomposites: CdSeS quantum dots and Au-N,S-GQD nanocomposites. For optical detection, the principle relies on the fluorescence quenching of CdSeS by Au-N,S-GQD in a sandwich structure with the target. Conversely, electrochemical detection is based on the change in impedance caused by the formation of the same sandwich structure. The biosensor demonstrated exceptional sensitivity, capable of detecting norovirus at concentrations of as low as femtomolar in the electrochemical method and picomolar in the optical method. In the dual-responsive concentration range from 10-13 to 10-10 M, the sensor is highly sensitive in both methods, creating significant changes in fluorescence intensity and impedance in the presence of virus. Furthermore, the biosensor exhibits a high degree of specificity, with a negligible response to nontarget proteins, even within complex test solutions. This work represents a significant advancement in the field of biosensor technology, offering a fast, accurate, and reliable method for diagnosing viral infections and diseases.

Simultaneous Electrochemical Detection of Cu2+ and Zn2+ in Pig Farm Wastewater.

In recent years, the rapid development of pig farming has led to a large quantity of heavy metal-polluted wastewater. Thus, it was desirable to develop a simple heavy metal detection method for fast monitoring of the wastewater from the pig farms. Therefore, there was an urgent need to develop a simple method for rapidly detecting heavy metal ions in pig farm wastewater. Herein, a simple electrochemical method for simultaneous detection of Cu2+ and Zn2+ was developed and applied to pig farm wastewater. With a glassy carbon electrode and anodic stripping voltammetry, simultaneous detection of Cu2+ and Zn2+ in water was achieved without the need for complicated electrode modification. Furthermore, it was found that the addition of Cd2+ can enhance the response current of the electrode to Zn2+, which increased the signal by eight times. After systematic optimization, the limit of detection (LOD) of 9.3 μg/L for Cu2+ and 45.3 μg/L for Zn2+ was obtained. Finally, it was successfully applied for the quantification of Cu2+ and Zn2+ with high accuracy in pig farm wastewater. This work provided a new and simple solution for fast monitoring of the wastewater from pig farms and demonstrated the potential of electrochemical measurement for application in modern animal husbandry.

Gold screen-printed electrodes coupled with molecularly imprinted conjugated polymers for ultrasensitive detection of streptomycin in milk

Antibiotic resistance is a global health threat, challenging traditional treatments and complicating the food safety process. This study introduces an electrochemical detection method for streptomycin sulfate, utilizing gold screen-printed electrodes (Au-SPE) functionalized via electropolymerization of a custom-made naphthalene diimide-based conjugated monomer (Th2-NDI-PIA). This modification creates specific binding sites for streptomycin, allowing rapid detection of the antibiotic. The sensor's response to different concentrations of streptomycin was studied via Differential Pulse Voltammetry (DPV) in a wide linear range from 10-13 M to 10-9 M, with a limit of detection (LoD) of 0.190 ± 0.005 pM. The imprinted electrode demonstrates selectivity to other antibiotics, but also to common interferents that can be found in milk such as lactose, glucose, riboflavin, and bisphenol A. Successful proof-of-principle in whole cow milk highlights the sensor's efficacy in detecting antibiotic residues in food samples, offering a promising alternative for a rapid and portable detection technique.

Peptide-Based Flavivirus Biosensors: From Cell Structure to Virological and Serological Detection Methods.

In tropical and developing countries, mosquito-borne diseases by flaviviruses pose a serious threat to public health. Early detection is critical for preventing their spread, but conventional methods are time-consuming and require skilled technicians. Biosensors have been developed to address this issue, but cross-reactivity with other flaviviruses remains a challenge. Peptides are essentially biomaterials used in diagnostics that allow virological and serological techniques to identify flavivirus selectively. This biomaterial originated as a small protein consisting of two to 50 amino acid chains. They offer flexibility in chemical modification and can be easily synthesized and applied to living cells in the engineering process. Peptides could potentially be developed as robust, low-cost, sensitive, and selective receptors for detecting flaviviruses. However, modification and selection of the receptor agents are crucial to determine the effectiveness of binding between the targets and the receptors. This paper addresses two potential peptide nucleic acids (PNAs) and affinity peptides that can detect flavivirus from another target-based biosensor as well as the potential peptide behaviors of flaviviruses. The PNAs detect flaviviruses based on the nucleotide base sequence of the target's virological profile via Watson-Crick base pairing, while the affinity peptides sense the epitope or immunological profile of the targets. Recent developments in the functionalization of peptides for flavivirus biosensors are explored in this Review by division into electrochemical, optical, and other detection methods.

Comparative study on mechanism of DC and AC current on corrosion of copper–aluminium composites

In this study, corrosion behaviours accelerated by neutral salt spray were thoroughly investigated on copper–aluminium composites with 3 wt% concentration NaCl for 72 h under DC and AC current respectively. The similarities and differences of the corrosion mechanism of the copper–aluminium composite under the two kinds of current were analysed by weight loss analysis, scanning electron microscopy, energy-dispersive X-ray spectroscopy and electrochemical detection methods. It can be concluded that there are two opposing influences of the current on the corrosive effects, including acceleration by the impressed current and inhibition by the heating effect. Of these, the inhibition effect on corrosion is more obvious, as the thermal effect of DC current is greater under the same current value. It is worth noting that the directional migration of ions caused by DC current will affect the degree of corrosion and the composition of the corrosion products on the surfaces of both sides of the samples, which is a unique characteristic not seen with AC current.

Progress and Challenge of Sensors for Dairy Food Safety Monitoring.

One of the most consumed foods is milk and milk products, and guaranteeing the suitability of these products is one of the major concerns in our society. This has led to the development of numerous sensors to enhance quality controls in the food chain. However, this is not a simple task, because it is necessary to establish the parameters to be analyzed and often, not only one compound is responsible for food contamination or degradation. To attempt to address this problem, a multiplex analysis together with a non-directed (e.g., general parameters such as pH) analysis are the most relevant alternatives to identifying the safety of dairy food. In recent years, the use of new technologies in the development of devices/platforms with optical or electrochemical signals has accelerated and intensified the pursuit of systems that provide a simple, rapid, cost-effective, and/or multiparametric response to the presence of contaminants, markers of various diseases, and/or indicators of safety levels. However, achieving the simultaneous determination of two or more analytes in situ, in a single measurement, and in real time, using only one working 'real sensor', remains one of the most daunting challenges, primarily due to the complexity of the sample matrix. To address these requirements, different approaches have been explored. The state of the art on food safety sensors will be summarized in this review including optical, electrochemical, and other sensor-based detection methods such as magnetoelastic or mass-based sensors.

Advances in Non-Enzymatic electrochemical materials for H2O2 sensing

With the progression of society, an increasing emphasis on physical well-being and environmental safety has driven extensive research into technologies closely aligned with human health and environmental protection. Hydrogen peroxide (H2O2), a representative reactive oxygen species (ROS), serves as one of the products resulting from the single electron reduction of oxygen in organisms, playing a crucial role in cell signaling and maintaining internal stability. Relevant alterations of H2O2 concentrations have been implicated in the pathogenesis of various diseases, including diabetes and cancer. Moreover, the utilization of H2O2 is widely prevalent in various industries including chemical, pharmaceutical, and food sectors. However, the repetitive or uncontrolled utilization of H2O2 engenders deleterious implications for human well-being and environmental integrity. Therefore, there is immense significance in exploring a simple yet effective method for real-time and quantitative detection of H2O2 in living cells and actual samples. The use of nanocatalysts as sensing materials in the electrochemical detection method has garnered significant attention from researchers due to their operational simplicity, high sensitivity, cost-effectiveness, and facile miniaturization. However, there remains a dearth of comprehensive reviews on the electrochemical detection of H2O2 utilizing nanomaterials. In this paper, we focus on summarizing contemporary techniques for H2O2 detection with a specific emphasis on electrochemical detection methods, and highlighting the significant advancements in the field of electrochemical detection of H2O2 nanomaterials while also providing insights into future developments.

Fluorescence-Recovered Wearable Hydrogel Patch for In Vitro Detection of Glucose Based on Rare-Earth Nanoparticles.

The physiological state of the human body can be indicated by analyzing the composition of sweat. In this research, a fluorescence-recovered wearable hydrogel patch has been designed and realized which can noninvasively monitor the glucose concentration in human sweat. Rare-earth nanoparticles (RENPs) of NaGdF4 doped with different elements (Yb, Er, and Ce) are synthesized and optimized for better luminescence in the near-infrared second (NIR-II) and visible region. In addition, RENPs are coated with CoOOH of which the absorbance has an extensive peak in the visible and NIR regions. The concentration of H2O2 in the environment can be detected by the fluorescence recovery degree of CoOOH-modified RENPs based on the fluorescence resonance energy transfer effect. For in vivo detection, the physiological state of oxidative stress at tumor sites can be visualized through its fluorescence in NIR-II with low background noise and high penetration depth. For the in vitro detection, CoOOH-modified RENP and glucose oxidase (GOx) were doped into a polyacrylamide hydrogel, and a patch that can emit green upconversion fluorescence under a 980 nm laser was prepared. Compared with the conventional electrochemical detection method, the fluorescence we presented has higher sensitivity and linear detection region to detect the glucose. This improved anti-interference sweat patch that can work in the dark environment was obtained, and the physiological state of the human body is conveniently monitored, which provides a new facile and convenient method to monitor the sweat status.

Emerging trends on nanomaterial-based simultaneous electrochemical sensing of dopamine and acetaminophen

Recent years have witnessed significant developments in electrochemical sensing, especially voltammetric techniques, which are known for providing flexible platforms for the simultaneous measurement of the analgesic acetaminophen (AC) and the neurotransmitter dopamine (DA). The most recent advancements and trends in electrochemical methods for the simultaneous detection of these two analytes are thoroughly reviewed in this paper. The different novel electrode materials, viz. nanostructures, and several surface modifications used to improve the sensitivity, selectivity, and stability of sensors that target the electrochemistry of acetaminophen and dopamine, have been carried out in studies published in the last decade. A wide range of voltammetric techniques are covered in this investigation, such as square wave voltammetry, differential pulse voltammetry, and cyclic voltammetry. The review also critically examines the drawbacks and restrictions of the existing approaches, which range from problems with selectivity in intricate matrices to the requirement for in-vivo applications and real-time monitoring in terms of diagnostics. The pursuit of multifunctional sensors, integration of advanced nanomaterials, and standardization of experimental conditions are identified as critical research gaps. The study concludes with some notions about potential future developments, highlighting the possible influence of current trends on the advancement of electrochemical sensors for the simultaneous measurement of dopamine and acetaminophen. It also suggests future directions for ongoing research and how the exploration of unexplored areas can be attended to develop highly sensitive, selective, and cost-effective electrochemical sensors.

The toxicity response of the electrochemical signal of the cell to the drug metabolized by the S9 system.

The electrochemical detection method of cytotoxicity using intracellular purines as biomarkers has shown great potential for in vitro drug toxicity evaluation. However, no electrochemical detection system based on an in vitro drug metabolism mechanism has been devised. In this paper, electrochemical voltammetry was used to investigate the effect of the S9 system on the electrochemical behavior of HepG2 cells, and benzo[a]pyrene, fluoranthene, and pyrene were employed to investigate the sensitivity of electrochemical signals of cells to the cytotoxicity of drugs metabolized by the S9 system. The results showed that, within 8 h of exposure to the S9 system, the electrochemical signal of HepG2 cells at 0.7 V did not alter noticeably. The levels of xanthine, guanine, hypoxanthine, and adenine in the cells were not significantly altered. Compared with the absence of S9 system metabolism, benzo[a]pyrene and fluoranthene processed by the S9 system decreased the electrochemical signal of the cells in a dose-dependent manner, while pyrene did not change it appreciably. HPLC also revealed that benzo[a]pyrene and fluoranthene metabolized by the S9 system decreased the intracellular purine levels, whereas pyrene had no effect on them before and after S9 system metabolism. The cytotoxicity results of the three drugs examined by electrochemical voltammetry and MTT assay showed a strong correlation and good agreement. The S9 system had no effect on the intracellular purine levels or the electrochemical signal of cells. When the drug was metabolized by the S9 system, variations in cytotoxicity could be precisely detected by electrochemical voltammetry.

Cobalt-nickel phosphide supported on reduced graphene oxide for sensitive electrochemical detection of bisphenol A

Bisphenol A (BPA) is a commonly utilized phenolic contaminant in several manufacturing processes, contributing to environmental pollution. Therefore, the detection of BPA holds significant importance for monitoring water quality. In this work, we report a robust electrochemical detection method for BPA utilizing cobalt−nickel bimetal phosphide nanoparticles (CoNiP) supported on reduced graphene oxide (rGO). The CoNiP@rGO-modified glassy carbon electrode exhibits remarkable electrochemical activity in BPA detection. The detection mechanism is controlled by adsorption-mediated electron transfer, showcasing a low limit of detection (LOD) at 0.38 nM and a high sensitivity of 96.4 A M−1 cm−2 within the linear range of 0.001–8 μM. Furthermore, our developed sensor demonstrates good reproducibility and successfully detected BPA in actual water samples. The electrochemical activity of CoNiP@rGO was also characterized for hydroquinone (HQ) detected through a diffusion-controlled mechanism, displaying an excellent sensitivity of 36.4 A M−1 cm−2 across a broad linear range. These findings underscore the promising potential of CoNiP@rGO as a candidate for electrochemical detection of phenolic contaminants, especially in the sensing of BPA in environmental water samples. This efficacy is attributed to the modulation of its electronic properties, combined with its large electroactive surface area and low electron-transfer resistance.

Electrochemistry detection of estrogenic effect: Regulation of de novo purine synthesis and catabolism by gibberellin and fulvestrant

The estrogenic effect of plant growth regulators has been received little attention, which leads to the lack of relevant toxicity data. In this study, the estrogenic effect induced by gibberellin with ERα-dependent manner was found by E-screen and western blot methods, and the electrochemical signals of MCF-7 cells regulated by gibberellin and fulvestrant were investigated. The results showed that the electrochemical signals of MCF-7 cells were increased by gibberellin, while reduced by fulvestrant significantly, and displayed an extremely sensitive response to the effects of estrogenic effect induced by ERα agonist and antagonist. Western blot results showed that the expressions of phosphoribosyl pyrophosphate amidotransferase and hypoxanthine nucleotide dehydrogenase in de novo purine synthesis and adenine deaminase in catabolism were more effective regulated by gibberellin and fulvestrant, resulting in significant changes of the levels of guanine, hypoxanthine and xanthine in cells, and then electrochemical signals. The results provide a theoretical basis for the establishment of new electrochemical detection method of the estrogenic effect of plant regulators.

An ultrasensitive electrochemical sensor for detecting Cd(II) in aquatic products based on CS/COFs/PEDOT: PSS modified acupuncture needle electrode

The use of low-cost working electrodes is of great importance for the development of sensor industrialization. Acupuncture needles electrode (ANE) was selected as working microelectrode, a sensor was designed based on poly(3,4-ethylenedioxythiophene)-polystyrene sulfonate (PEDOT: PSS) and chitosan (CS) modified covalent organic frameworks (COFs) (CS/COFs) for detection of cadmium (Cd(II)). First, a mixture of PEDOT and PSS was electrodeposited on the surface of the acupuncture needles to synthesize a PEDOT: PSS as conductive polymeric film to support the electron transfer capability and enhance the conductive efficiency of the sensor. Then, CS/COFs was self-assembled and attached to the PEDOT: PSS/ANE surface by π-π stacking intermolecular interaction forces and the viscosity of CS, thus increasing the specific surface area of the electrode. Differential pulse anodic stripping voltammetry (DPASV) was used as the electrochemical method for detection of Cd(II). And the results indicated that the CS/COFs/PEDOT: PSS/ANE was linearly responsive in the range of 400 μg/L to 2400 μg/L, and the LOD was 13.8 ng/L for Cd(II). The constructed sensor also showed great selectivity, reproducibility, and stability. Additionally, the sensor demonstrated outstanding recovery in the detection of Cd(II) in real sample scallops. This sensing construction method based on acupuncture needles as working electrodes is of great significance to the development of sensor industrialization and aquatic product safety detection.

Electrochemical Method for Detection and Quantification of Lead Particulate in Tap Water

Quantification of lead particulates requires laborious sample acidification and/or digestion in acidic environment, therefore lead quantification is limited to laboratories with trained personnel and expensive instrumentation. These technologies are not easily accessible to the public, and the large number of portable methods available to public today are characterized by their qualitative nature, and requirement of additional reagents. Unlike labor intense expensive instruments, electrochemical methods are inexpensive, fast and portable but they are blind to non-electroactive lead species or particulate forms of lead. They are limited to the detection of ionic or electroactive analytes. This talk will report an electrochemical method for the detection and quantification of lead contaminant in drinking waters that results from particulate forms of lead, mostly present as scales. We will present the fundamentals of membrane electrolysis for reagent-free sample preparation and detection of Pb2+. Also, we will present the characterization of real particulates/scales extracted from lead service lines from the Cincinnati area. We think this method will contribute to the development of on-site, quantitative methods of lead detection, and can assist to the research and understanding of drinking water contamination. Perhaps it could help to determine what triggers lead intermittent release to residential tap water. This work has the potential to address the lack of that instrumentation because it employs a robust technology based on anionic exchange membrane and controlled electrolysis for in-situ generation of nitric acid, that eliminates the need of external reagent or sample treatments. For its trace detection, it employs a well stablished Anodic Striping Voltammetry method.

Electrochemistry-Based Diagnosis of Li Plating for Fast-Charging Li-Ion Batteries

Recent innovations in battery technologies have facilitated the development and widespread use of electric vehicles (EVs), by increasing the energy density of batteries while lowering their cost. Despite the rapid growth of the EV market, the long charging time of lithium-ion batteries (LIBs) remains as a major obstacle for expanding customer acceptance of EVs. Typically, graphite-based anodes in the state-of-the-art LIBs suffer from Li plating under fast-charging conditions, which causes severe performance degradations and early cell failure of batteries. To prevent the Li plating-induced failure, extensive research efforts have been devoted to developing diagnostic methods capable of detecting Li plating. The electrochemical analysis of Li plating enables non-destructive, in operando detection without complicated experimental procedures or special equipment.Herein, we present a non-destructive method for detecting Li plating during fast-charge cycling by analyzing current transients during the constant-voltage charging step, based on electrochemical battery models. Three-dimensional (3D) and pseudo-two-dimensional (P2D) battery models are employed to predict the electrochemical behavior of full cells under fast-charging conditions. 3D model enables the evaluation of local electrochemical properties, such as local reaction current densities and electrode potentials, which are largely affected by the microstructure of the electrode. Furthermore, P2D models are employed to investigate the effect of changes in microstructural properties (e.g., porosity and fraction of active surface of the graphite anode) on electrochemical behavior of full cells.For 3D modeling, the 3D Voronoi tessellation and Catmull-Clark algorithm are employed to construct the model geometry of graphite anodes. 3D modeling results predict that upon fast-charging, the charge-transfer potential on the top surface of graphite anode rapidly drops below 0 V vs. Li/Li+, triggering Li plating. To extract the electrochemical signals of Li plating, the fast-charging behaviors of full cells are investigated by using the P2D model with a partially reversible Li plating–stripping reaction. In specific, the constant-current and constant-voltage (CC-CV) charging process of the full cells with graphite anodes is simulated with Li plating-induced degradation modes; reduction of (i) interparticle pores, (ii) active surface area for Li intercalation reaction, and (iii) cyclable Li amount. Modeling results demonstrate that an inflection point appears in the current transient curve, and it shows a positive shift when the Li plating-induced degradation occurs. Electrochemical tests and microstructural analyses further confirm the validity of proposed electrochemical detection of Li plating. This study provides an effective strategy to design electrochemical methods for Li plating detection during fast-charging batteries based on electrochemistry-based models.

Nanopore electrochemical sensors for emerging hazardous pollutants detection

Nanopore electrochemical sensors have been developed to detect various emerging pollutants at the single-molecule level with high sensitivity and specificity due to their high resolution in past three decades, which is of great significance for emerging hazardous pollutants control. Electrochemical detection methods based on nanopore technology are primarily divided into two categories: resistive-pulse and rectification sensing. The main detection mechanism of the resistive-pulse method is based on the volume exclusion effect generated when the analyte enters through the nanopore, and it involves three primary detection strategies. The first approach involves nanopore technology for direct pollutant detection, where pollutant structure and concentration information is assessed based on nanopore-generated ionic current's blockade strength, duration, and frequency. The second strategy relies on weak intermolecular interactions when direct detection of pollutants is challenging. Molecular probes interact with target molecules to enhance detection sensitivity and achieve specific recognition. The third strategy is based on the biological/chemical reaction of pollutant molecules, through indirect detection method to achieve specific detection of target pollutant molecules. Additionally, relies on changes in surface charge polarity or nanopore spatial structure induced by the analyte molecules to achieve the detection of target molecules within the nanopore. This work demonstrates the research progress achieved in the application of nanopore electrochemical sensing technology to high-sensitivity detection of hazardous pollutants, utilizing the unique confined spatial characteristics of nanopores, combined with biorecognition techniques and principles of electrochemical reactions.

4-Aminophenylboronic acid dimer sensitized carbon nanotubes for the construction of portable and disposable sulfide electrochemical sensors

Abnormal sulfide levels in serum can cause kidney failure, Alzheimer's, Parkinson's, stroke, diabetes, and even cancer. Therefore, maintaining proper sulfide balance is crucial for managing and preventing these conditions. Electrochemical approaches have emerged as potential alternatives for sulfide detection. However, the adsorption of elemental sulfur on the working electrode leads to surface fouling and passivation, posing a significant challenge in developing reliable electrochemical methods for sulfide detection. In this study, we present a portable and surface fouling-free electrochemical system that utilizes functionalized multi-walled carbon nanotubes and 4-aminophenylboronic acid dimers for accurate sulfide measurement. The sensor showed excellent electrocatalytic activity to sulfide and antifouling activity to possible interferences. The method had a linear range from 10 µM to 2 mM and a detection limit of 2.3 µM. The effectiveness and applicability of this method were evaluated by analyzing sulfide levels in different serum samples and comparing the results with their glucose levels. As both blood glucose and sulfide levels can serve as indicators of certain health conditions, such as diabetes or sulfur metabolism disorders, this comparison provides valuable insights. Importantly, no complicated sample pretreatment was involved, thus this method can be easily adopted as a point-of-care diagnostic device. Additionally, the study also revealed a higher concentration of sulfide in cancer cells than in normal cells, offering a new development direction for differentiating between cancer cells and normal cells.

A label-free electrochemical biosensor based on PBA-Au-MXene QD for miR-122 detection in serum samples.

Apoly(n-butyl acrylate)-gold-MXene quantum dots (PBA-Au-MXene QD) nanocomposite-based biosensor is presentedthat is modified by unique antisense single-stranded DNA (ssDNA) and uses the electrochemical detection methods of DPV, CV, and EIS to early detect miR-122 as a breast cancer biomarker in real clinical samples. This fabrication method is based on advanced nanotechnology, at which a poly(n-butyl acrylate) (PBA) as a non-conductive polymer transforms into a conductive composite by incorporating Au-MXene QD. This biosensor had a limit of detection (LOD) of 0.8 zM and a linear range from 0.001 aM to 1000 nM, making it capable of detecting the low concentrations of miR-122 in patient samples. Moreover, it allows approximately 100% sensitivity and 100% specificity for miR-122 without extraction. The synthesis and detection characteristics were evaluated by different complementary tests such as AFM, FTIR, TEM, and FESEM. This new biosensor can have a high potential in clinical applications to detect breast cancer early and hence improve patient outcomes.

The Development and Full Validation of a Novel Liquid Chromatography Electrochemical Detection Method for Simultaneous Determination of Nine Catecholamines in Rat Brain.

Chemical neurotransmission, managed by neurotransmitters, has a crucial role in brain processes such as fear, memory, learning, and pain, or neuropathology such as schizophrenia, epilepsy, anxiety/depression, and Parkinson's disease. The measurement of these compounds is used to elucidate the disease mechanisms and evaluate the outcomes of therapeutic interventions. However, this can be quite difficult because of various matrix effects and the problems of chromatographic separation of analysts. In the current study; for the first time, an optimized and fully validated high-performance liquid chromatography-electrochemical detection (HPLC-EC) method according to Food and Drug Administration and European Medicines Agency Bioanalytical Validation Guidance was developed for the simultaneous analysis of nine neurotransmitter compounds, namely dopamine, homovanilic acid, vanilmandelic acid, serotonin (SER), 5-hydroxyindole-3-acetic acid, 4-hydroxy-3-methoxyphenylglycol, norepinephrine, 3,4 dihydroxyphenylacetic acid, and 3-methoxytyramine and simultaneously determined in rat brain samples. Separation was achieved with 150 mm x 4.6 mm, 2.6 μm Kinetex F5 (Phenomenex, USA) column isocratically, and analysis was carried out by HPLC equipped with a DECADE II EC detector. The method exhibited good selectivity, and the correlation coefficient values for each analyte's calibration curves were > 0.99. The detection and quantification limits ranged from 0.01 to 0.03 ng/mL and 3.04 to 9.13 ng/mL, respectively. The stability of the analyses and method robustness were also examined in detail in the study, and the obtained results are presented statistically. The developed and fully validated method has been successfully applied to actual rat brain samples, and important results have been obtained. In the rat brain sample analysis, the lowest number of SER and the highest amount of noradrenaline were found.