Graphene derivative-based ink advances inkjet printing technology for fabrication of electrochemical sensors and biosensors.

The field of biosensing would significantly benefit from a disruptive technology enabling flexible manufacturing of uniform electrodes. Inkjet printing holds promise for this, although realizing full electrode manufacturing with this technology remains challenging. We introduce a nitrogen-doped carboxylated graphene ink (NGA-ink) compatible with commercially available printing technologies. The water-based and additive-free NGA-ink was utilized to produce fully inkjet-printed electrodes (IPEs), which demonstrated successful electrochemical detection of the important neurotransmitter dopamine. The cost-effectiveness of NGA-ink combined with a total cost per electrode of $0.10 renders it a practical solution for customized electrode manufacturing. Furthermore, the high carboxyl group content of NGA-ink (13 wt%) presents opportunities for biomolecule immobilization, paving the way for the development of advanced state-of-the-art biosensors. This study highlights the potential of NGA inkjet-printed electrodes in revolutionizing sensor technology, offering an affordable, scalable alternative to conventional electrochemical systems.

Organic photoelectrochemical transistor aptasensor for dual-mode detection of DEHP with CRISPR-Cas13a assisted signal amplification.

Emerging organic photoelectrochemical transistors (OPECTs) with inherent amplification capabilities, good biocompatibility and even self-powered operation have emerged as a promising detection tool, however, they are still not widely studied for pollutant detection. In this paper, a novel OPECT dual-mode aptasensor was constructed for the ultrasensitive detection of di(2-ethylhexyl) phthalate (DEHP). MXene/In2S3/In2O3 Z-scheme heterojunction was used as a light fuel for ion modulation in sensitive gated OPECT biosensing. A transistor system based on poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) converted biological events associated with photosensitive gate achieving nearly a thousand-fold higher current gain at zero bias voltage. This work quantified the target DEHP by aptamer-specific induction of CRISPR-Cas13a trans-cutting activity with target-dependent rolling circle amplification as the signal amplification unit, and incorporated the signal changes strategy of biocatalytic precipitation and TMB color development. Combining OPECT with the auxiliary validation of colorimetry (CM), high sensitivity and accurate detection of DEHP were achieved with a linear range of 0.1 pM to 200 pM and a minimum detection limit of 0.02 pM. This study not only provides a new method for the detection of DEHP, but also offers a promising prospect for the gating and application of the unique OPECT.

Swellable microneedle-coupled light-addressable photoelectrochemical sensor for in-situ tracking of multiple pesticides pollution in vivo.

In vivo monitoring of multiple pesticide contamination is of great significance for evaluating the health risks of different pesticides, agricultural production safety, and ecological and environmental assessment. Here, we report a hydrogel microneedle array coupled light-addressable photoelectrochemical sensor for tracking multiple pesticide uptake and elimination in living animals and plants, holding three prominent merits: i) enables in-situ detection of in vivo pesticides, avoiding cumbersome and complex sample transportation and handling processes; ii) allows repeated in vivo sampling of the same organism, improving tracking test controllability and accuracy; iii) avoids lethal sampling, providing a better understanding of the pesticides fate in living organisms. The coupled sensor is mechanically robust for withstanding more than 0.35 N per needle and highly swellable (800 %) for timely extraction of sufficient in vivo solution for analysis. For proof-of-concept, it achieves in-situ detection of atrazine, acetamiprid, and carbendazim efficiently and quantitatively in artificial agarose skin models, mouse skin interstitial fluids, and plant leaves with little inflammatory reaction. This simple, highly integrated, minimally invasive, and high-throughput in vivo monitoring method is ideal for future field environmental monitoring and plant and animal disease diagnosis.

One-step electrodeposited hybrid nanofilms in amperometric biosensor development.

This review summarizes recent developments in amperometric biosensors, based on one-step electrodeposited organic-inorganic hybrid layers, used for analysis of low molecular weight compounds. The factors affecting self-assembly of one-step electrodeposited films, methods for verifying their composition, advantages, limitations and approaches affecting the electroanalytical performance of amperometric biosensors based on organic-inorganic hybrid layers were systemized. Moreover, issues related to the formation of one-step organic-inorganic hybrid functional layers with different structures in biosensors produced under the same electrodeposition parameters are discussed. The systemized dependencies can support the preliminary choice of functional sensing layers with architectures tuned for specific biotechnology and life science applications. Finally, the capabilities of one-step electrodeposition of organic-inorganic hybrid functional films beyond amperometric biosensors were highlighted.

A novel electrode for simultaneous detection of multiple heavy metal ions without pre-enrichment in food samples.

Integrating a pre-enrichment step into electrochemical detection methodologies has traditionally been employed to enhance the performance of heavy metal detection. However, this augmentation also introduces a degree of intricacy into the sensing process and increases energy consumption. In this work, Mo-doped WO3 is grown in situ on carbon cloth by one-step electrodeposition. The electrode detect multiple heavy metal ions simultaneously in the range of 0.1-100.0 µM with LODs ranging from 11.2 to 17.1 nM. The electrode successfully detected heavy metal ions in diverse food samples. This pioneering detection strategy realized the direct and simultaneous detection of multiple heavy metal ions by utilizing the valence property of WO3 and oxygen vacancies generated by molybdenum doping. The Mo-WO3/CC pre-enrichment-free detection electrode boasts straightforward preparation, a streamlined detection procedure, swift response kinetics, and superior performance relative to previously reported electrodes, which makes it possible to develop a portable heavy metal ion detection device.

Construction of a self-reporting molecularly-imprinted electrochemical sensor based on CuHCF modified by rGNR-rGO for the detection of zearalenone.

A self-reporting molecularly-imprinted electrochemical sensor is prepared for the detection of Zearalenone (ZEA). Firstly, the reduced graphene nanoribbons and reduced graphene oxide (rGNR-rGO) were simultaneously modified onto a glassy carbon electrode (GCE) to improve the sensor's sensitivity. After electrodepositing copper nanoparticles onto the rGNR-rGO/GCE, cyclic voltammetry scanning was performed in potassium ferrocyanide solution, and copper hexacyanoferrate (CuHCF) was deposited onto rGNR-rGO/GCE to further improve the sensor's sensitivity while giving it self-reporting capability. Then, molecularly-imprinted polymer films were prepared on the CuHCF/rGNR-rGO/GCE to ensure the selectivity of the sensor. It is found that the linear range of ZEA detection by the constructed sensor is 0.25-500 ng·mL -1, with a detection limit of 0.09 ng·mL -1. This sensor shows the merits of good selectivity, high sensitivity and accurate detection, providing a great possibility for the precise detection of low concentration ZEA in food.

A novel electrochemical aptasensor based on polyaniline and gold nanoparticles for ultrasensitive and selective detection of ascorbic acid.

Ascorbic acid (AA) is involved in many physiological activities of the body and plays an important role in maintaining and promoting human health. It is also present in many natural and artificial foods. Therefore, the development of highly sensitive and accurate AA sensors is highly desirable for human health monitoring, as well as other commercial application fields. Herein, an ultrasensitive and selective electrochemical sensor based on an aptamer was developed for the determination of AA for the first time. The aptasensor was fabricated by modifying a composite made of polyaniline (PANI) and gold nanoparticles (AuNPs) on a glassy carbon electrode. The morphologies and electrochemical properties of the resulting electrodes were characterized by various analytical methods. The results indicated relatively good electrical conduction properties of PANI for accelerated electron transfer. The modification with AuNPs provided signal amplification, suitable for applications as novel platforms for the sensitive sensing of AA. Under optimized conditions, the proposed aptasensor displayed a wide linear response toward the detection of AA from 1.0 to 1.0 × 105 ng L-1 coupled with a low detection limit of 0.10 ng L-1. The sensor also exhibited excellent selectivity and high stability, with at least 2000-fold higher sensitivity than similar previously reported methods. Importantly, the aptasensor exhibited promising properties for the determination of AA in real fruits, vegetables, and infant milk powder, thereby showing potential for food analysis.

The Smart Drifter Cluster: Monitoring Sea Currents and Marine Litter Transport Using Consumer IoT Technologies.

The study of marine Lagrangian transport holds significant importance from a scientific perspective as well as for practical applications such as environmental-pollution responses and prevention (e.g., oil spills, dispersion/accumulation of plastic debris, etc.). In this regard, this concept paper introduces the Smart Drifter Cluster: an innovative approach that leverages modern "consumer" IoT technologies and notions. This approach enables the remote acquisition of information on Lagrangian transport and important ocean variables, similar to standard drifters. However, it offers potential benefits such as reduced hardware costs, minimal maintenance expenses, and significantly lower power consumption compared to systems relying on independent drifters with satellite communication. By combining low power consumption with an optimized, compact integrated marine photovoltaic system, the drifters achieve unlimited operational autonomy. With the introduction of these new characteristics, the Smart Drifter Cluster goes beyond its primary function of mesoscale monitoring of marine currents. It becomes readily applicable to numerous civil applications, including recovering individuals and materials at sea, addressing pollutant spills, and tracking the dispersion of marine litter. An additional advantage of this remote monitoring and sensing system is its open-source hardware and software architecture. This fosters a citizen-science approach, enabling citizens to replicate, utilize, and contribute to the improvement of the system. Thus, within certain constraints of procedures and protocols, citizens can actively contribute to the generation of valuable data in this critical field.

Electrochemical sensor applying ZrO2/nitrogen-doped three-dimensional porous carbon nanocomposite for efficient detection of ultra-trace Hg2+ ions.

In this study, a ZrO2/nitrogen-doped three-dimensional porous carbon (ZrO2/N-3DPC) nanocomposite was manufactured to fabricate an effective electrochemical sensor for the detection of ultra-trace mercury ion (Hg2+). The synthesized N-3DPC had an open pore structure, large specific surface area and enough continuous mass transfer channels, which can facilitate the diffusion and transmission of electrons and ions at the sensing interface, providing an effective adhesion platform for electrochemical deposition of ZrO2 nanoparticles. Benefiting from the synergistic effect of ZrO2 and N-3DPC, the developed electrochemical sensor had good adsorption and catalytic performance for Hg2+ with a wider linear range of 0.1-220 µg L-1 and a lower detection limit of 0.062 µg L-1. Meanwhile, the sensor exhibited remarkable repeatability, reproducibility, stability and anti-interference, and was further applied to detect Hg2+ in seafood and tap water with satisfactory recoveries (97.1-103.1%) and lower relative standard deviation (≤4.3%). The proposed strategy of electrochemical sensing detection of Hg2+ provides a new idea and direction for the research of ZrO2/N-3DPC nanocomposite in the field of analysis and detection, which is also of great significance to ensure foods, environmental safety and human health.

Application of a Screen-Printed Sensor Modified with Carbon Nanofibers for the Voltammetric Analysis of an Anticancer Disubstituted Fused Triazinone.

In this paper, we propose the first analytical procedure-using a screen-printed carbon electrode modified with carbon nanofibers (SPCE/CNFs)-for the detection and quantitative determination of an electroactive disubstituted fused triazinone, namely 4-Cl-PIMT, which is a promising anticancer drug candidate. The electrochemical performances of the sensor were investigated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and square-wave adsorptive stripping voltammetry (SWAdSV). The presence of carbon nanofibers on the sensor surface caused a decrease in charge-transfer resistance and an increase in the active surface compared to the bare SPCE. Under the optimised experimental conditions, the proposed voltammetric procedure possesses a good linear response for the determination of 4-Cl-PIMT in the two linear ranges of 0.5-10 nM and 10-100 nM. The low limits of detection and quantification were calculated at 0.099 and 0.33 nM, respectively. In addition, the sensor displays high reproducibility and repeatability, as well as good selectivity. The selectivity was improved through the use of a flow system and a short accumulation time. The SWAdSV procedure with SPCE/CNFs was applied to determine 4-Cl-PIMT in human serum samples. The SWAdSV results were compared to those obtained by the ultra-high-performance liquid chromatography coupled with electrospray ionization/single-quadrupole mass spectrometry (UHPLC-ESI-MS) method.

TBISTAT: An open-source, wireless portable, electrochemical impedance spectroscopy capable potentiostat for the point-of-care detection of S100B in plasma samples.

Point-of-Care (POC) testing for biomarker detection demands techniques that are easy to use, readily available, low-cost, and with rapid response times. This paper describes the development of a fully open-source, modular, wireless, battery-powered, smartphone-controlled, low-cost potentiostat capable of conducting electrochemical impedance spectroscopy for the electrochemical detection of the S100B protein captured in an ANTI-S100B functionalized thin-film gold interdigitated electrode platform to support traumatic brain injury diagnosis and treatment. EIS results from the developed potentiostat were validated with a commercial benchtop potentiostat by comparing impedance magnitude and phase values along the EIS frequency range. In addition, an experimental design was performed for detecting S100B in spiked human plasma samples with S100B concentrations of clinical utility, and a calibration curve was found for quantifying S100B detection. No statistically significant differences were found between EIS results from the developed potentiostat and the commercial potentiostat. Statistically significant differences in the changes in charge transfer resistance signal between each tested S100B concentration (p < 0.05) were found, with a limit of detection of 35.73 pg/mL. The modularity of the proposed potentiostat allows easier component changes according to the application demands in power, frequency excitation ranges, wireless communication protocol, signal amplification and transduction, precision, and sampling frequency of ADC, among others, when compared to state-of-the-art open-source EIS potentiostats. In addition, the use of minimal, easy acquirable open-source hardware and software, high-level filtering, accurate ADC, Fast Fourier Transform with low spectral leakage, wireless communication, and the simple user interface provides a framework for facilitating EIS analysis and developing new affordable instrumentation for POC biosensors integrated systems.

Highly Stable Buffer-Based Zinc Oxide/Reduced Graphene Oxide Nanosurface Chemistry for Rapid Immunosensing of SARS-CoV-2 Antigens.

The widespread and long-lasting effect of the COVID-19 pandemic has called attention to the significance of technological advances in the rapid diagnosis of SARS-CoV-2 virus. This study reports the use of a highly stable buffer-based zinc oxide/reduced graphene oxide (bbZnO/rGO) nanocomposite coated on carbon screen-printed electrodes for electrochemical immuno-biosensing of SARS-CoV-2 nuelocapsid (N-) protein antigens in spiked and clinical samples. The incorporation of a salt-based (ionic) matrix for uniform dispersion of the nanomixture eliminates multistep nanomaterial synthesis on the surface of the electrode and enables a stable single-step sensor nanocoating. The immuno-biosensor provides a limit of detection of 21 fg/mL over a linear range of 1-10 000 pg/mL and exhibits a sensitivity of 32.07 ohms·mL/pg·mm2 for detection of N-protein in spiked samples. The N-protein biosensor is successful in discriminating positive and negative clinical samples within 15 min, demonstrating its proof of concept used as a COVID-19 rapid antigen test.

Electrochemical quantification of mancozeb through tungsten oxide/reduced graphene oxide nanocomposite: A potential method for environmental remediation.

The extensive use of pesticides for better yield of crops have become major human concern over the decades. Pesticides are widely used in the fields to kill weeds and pests on the vegetable and crops to improve the quality and yield of the food knowing the fact that pesticides residue in food are very lethal for human being. Amongst, the hazardous pesticides, mancozeb is widely applied in the protection of crops. Thus the quantification of mancozeb residue is of great importance. This study reports the electrochemical monitoring of mancozeb through tungsten oxide reduced graphene oxide (WO3/rGO) nanocomposite. The engineered nanocomposite was characterized though different analytical tools such as FTIR, XRD and TEM to examine crystallinity, internal texture and the size. The FTIR result confirm the functionalities of GO and WO3/rGO nanocomposite in finger print and functional group region. Through XRD analysis, the size of the WO3/rGO nanocomposite was calculated as 31.6 nm. While the TEM analysis was also exploited to examine the 2D texture of GO and nanometric size of the WO3/rGO. To ensure the conductive nature of the WO3/rGO nanocomposite, the glassy carbon electrode was modified and exploited for cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under the optimal conditions, the modified sensor showed exceptional response for mancozeb. The linear dynamic range was set from 0.05 to 70 µM in BRB buffer of pH 4. The LOD and LOQ for proposed method was calculated as 0.0038 and 0.0115 µM. The analytical applicability of chemically modified sensor was investigated in real matrix of different vegetable samples and the recovery values were observed in acceptable range. The electrochemical examination of present work reveals that WO3/rGO nanocomposite can be an exceptional aspirant for the determination of mancozeb at commercial level.

Portable electrochemical micro-workstation platform for simultaneous detection of multiple Alzheimer's disease biomarkers.

Alzheimer's disease, as a most prevalent type of dementia, is quickly becoming one of the most expensive, lethal, and burdening diseases of this century. Though there are still no efficient therapies, early diagnosis and intervention are important directive significance to clinical works. Here, we develop a portable electrochemical micro-workstation platform consisting of an electrochemical micro-workstation and integrated electrochemical microarray for simultaneously detecting multiple AD biomarkers including Aß40, Aß42, T-tau, and P-tau181 in serum. The integrated electrochemical microarray is mainly used for droplet sample manipulation and signal generation. The micro-workstation can regulate signals and transfer the signals to a smartphone by Bluetooth embedded inside. This portable electrochemical micro-workstation platform exhibits excellent analysis performance. The LODs for Aß40, Aß42, T-tau, and P-tau181 are 0.125 pg/mL, 0.089 pg/mL, 0.142 pg/mL, and 0.176 pg/mL, respectively, which satisfies the needs of detecting AD biomarkers in serum. The combination of portable micro-workstation and integrated electrochemical microarray provides a promising strategy for the early diagnosis of Alzheimer's disease and personal healthcare.

Numerical Simulation of S-Shaped Current-Voltage Curves Induced by Electron Traps in Inverted Organic Photovoltaics.

Organic photovoltaics (OPVs) differ from their inorganic counterparts because of inevitable electronic disorders and structural heterogeneity. Charge carrier traps are inevitable in organic semiconductors. A common failure mechanism of OPVs is the development of an S-shaped current density-voltage characteristic (J-V curve). Herein, we focus on investigating the underlying physical mechanism of S-shaped deformation of J-V curve of the inverted organic photovoltaic devices with bulk-heterojunction, proven by experiments with the n-doped electron extraction layer and numerical simulations assuming electron traps (0.1 eV deeper) in the electron extraction layer. The numerical simulations are quite consistent with the experimental results. In addition, the open circuit voltage induced by S-kink is exemplified to be enhanced after removing the electron traps in the interlayer by introducing a dopant of cesium carbonate.

Fabrication of rGO/MXene-Pd/rGO hierarchical framework as high-performance electrochemical sensing platform for luteolin detection.

A  nanocomposite of rGO/MXene-Pd/rGO with hierarchical structure based on Ti3C2Tx MXene, Pd nanoparticles, and reduced graphene oxide (rGO) was synthesized by a green approach. Ti3C2Tx MXene decorated with Pd nanoparticles (MXene-Pd) was prepared first. Then, graphene oxide (GO), MXene-Pd, and GO were coated on the surface of the glassy carbon electrode (GCE) in sequence. After each coating of the GO layer, the GO nanosheets were reduced to rGO electrochemically. The fabricated rGO/MXene-Pd/rGO hierarchical framework performs a pie structure with MXene-Pd as the stuffing and rGO nanosheets as the crust, which will be beneficial to the enhancement of its electrochemical sensing performance. As compared with other electrodes, the rGO/MXene-Pd/rGO/GCE exhibited higher electrocatalytic activity and better sensing performance for luteolin detection, with a wide linear range of 6.0 × 10-10 to 8 × 10-7 M and 1.0 × 10-6 to 1.0 × 10-5 M (oxidation peak potential Epa = 0.34 V vs. SCE), a low detection limit of 2.0 × 10-10 M, and a high sensitivity of 112.72 µA µM-1 cm-2. Moreover, the fabricated sensor also showed high selectivity, reproducibility, and repeatability toward the detection of luteolin. The real sample analysis for luteolin in honeysuckle was successfully carried out by rGO/MXene-Pd/rGO and verified with high-performance liquid chromatography (HPLC) analysis techniques with acceptable results. All the above tests indicate the promising application prospect of the rGO/MXene-Pd/rGO framework for luteolin detection in honeysuckle and other herbs containing luteolin.

Three-dimensional graphene/amino-functionalized metal-organic framework for simultaneous electrochemical detection of Cd(II), Pb(II), Cu(II), and Hg(II).

Trace detection of multiple toxic heavy metals is a very important and difficult problem, conveniently, sensitively, and reliably. In this work, we developed an innovative electrochemical sensor for simultaneously detected heavy metal ions (Cd2+, Hg2+, Cu2+, and Pb2+). In order to detect trace amounts of Cd(II), Pb(II), Cu(II), and Hg(II) in food quickly, accurately, and at low cost, this study used electrochemical reduction to prepare a screen-printed electrode (3DGO) modified with 3DGO and UiO-66-NH2 composite nanomaterials (UiO-66-NH2/SPCE). The sensing platform is composed of three-dimensional graphene (3DGO), aminated UiO-66 metal-organic framework, named 3DGO/UiO-66-NH2. It is worth noting that the porous structure, amino functional groups on the surface, and large specific surface area of UiO-66-NH2 can enrich and promote the absorption of heavy metal ions. 3DGO was introduced to improve the electrochemical activity and conductivity of UiO-66-NH2 material. The construction of this new sensing platform, which can synchronously, reliably, and sensitively simultaneously detect Cd2+, Pb2+, Cu2+, and Hg2+ only in 150 s in the linear range of 0.01-0.35 pM with the detection limitations, is 10.90 fM, 5.98 fM, 2.89 fM, and 3.1 fM, respectively. This method provides a new strategy that uses MOF materials for electrochemical detection of a variety of heavy metal ions in food.

Electrochemical determination of several biofuel antioxidants in biodiesel and biokerosene using polylactic acid loaded with carbon black within 3D-printed devices.

Low oxidation stability is the main drawback of biodiesels and biokerosenes that is overcome by using antioxidants, which can be combined due to synergistic effects. This paper demonstrates that 3D-printed electrochemical devices can be applied to biofuel electroanalysis, including the monitoring of oxidation stability by quantifying the antioxidant content in biofuels. Fabrication requires 3D-printed acrylic templates at which a polylactic acid (PLA) filament with conducting carbon-black filling sensors is extruded by a 3D pen. The antioxidants butyl hydroxyanisole (BHA) and tert-butylhydroquinone (TBHQ) are the most employed additives in biodiesel production, and thus, their electrochemical behavior was investigated; 2,6-ditertbutylphenol (2,6-DTBP) was included in this investigation because it is commonly added to biokerosenes. The electrochemical surface treatment of the 3D-printed electrodes improved the current responses of all antioxidants; however, the electrochemical oxidation of TBHQ was clearly more affected by an electrocatalytic action shifting its oxidation towards less positive potentials (~200 mV), which resulted in a better separation of TBHQ and BHA oxidation peaks (+0.4 and +0.6 V vs Ag|AgCl, respectively). The oxidation of 2,6-DTBP occurred at more positive potentials (+1.2 V vs Ag|AgCl). The simultaneous determination of TBHQ and BHA by differential-pulse voltammetry resulted in linear responses in the range 0.5 and 175 µmol L-1 with limits of detection and quantification of 0.15 µmol L-1 and 0.5 µmol L-1, respectively. The presence of Fe3+, Cu2+, Pb2+, Mn2+, Cd2+, and Zn2+, even in high concentrations, did not interfere in the determination of TBHQ and BHA. The determination of 2,6-DTBP in biokerosene was achieved by cyclic voltammetry. All relative standard deviations (RSD) were lower than 6.0 %, indicating adequate precision of the methods. Spiked biofuel samples were analyzed (after dilution in electrolyte) and recovery values between 85 and 120% were obtained, which indicates absence of sample matrix effects.

Multiplexed and simultaneous biosensing in a 3D-printed portable six-well smartphone operated electrochemiluminescence standalone point-of-care platform.

3D-printed portable devices have immense and proven potential to transform the field of electrochemiluminescence (ECL) for diverse biochemical applications. 3D printing (3DP) offers unparalleled ability to build tiny devices in a single step with high accuracy and compatibility, and integrability as per the requirement. In this study, for the first time, a six-well 3D-printed closed bipolar electrochemiluminescence (3DP-CBPE-ECL) device has been successfully fabricated and validated by performing single-step detection of various biochemicals such as glucose and choline. Luminol/H2O2-based enzymatic reactions were performed with optimized parameters for selective sensing of glucose and choline. The single-step detection of glucose and choline was accomplished for the linear ranges of 0.1 to 10 mM and 0.1 to 5 mM, with a limit of detections (LODs) of 24 µM and 10 µM, respectively. A smartphone was leveraged to execute multiple activities such as powering the ECL device, capturing ECL images, and calculating the ECL intensity of the obtained ECL signal. The feasibility of a six-well 3DP-CBPE-ECL device was tested by sensing glucose and choline simultaneously in a single device at three different concentrations. Furthermore, the concentration of glucose and choline was calculated in real blood serum using the conventional additive (spiking) method, demonstrating the high practicability of the fabricated ECL device and yielding promising findings. Finally, based on the obtained results and other advantages such as low-cost, fast prototyping and requirement of a minimum sample volume, the fabricated six-well 3DP-CBPE-ECL device has shown potential to be used in the field of biochemical applications.

T7 Endonuclease I-mediated voltammetric detection of KRAS mutation coupled with horseradish peroxidase for signal amplification.

Rapid and selective sensing of KRAS gene mutation which plays a crucial role in the development of colorectal, pancreatic, and lung cancers is of great significance in the early diagnosis of cancers. In the current study, we developed a simple electrochemical biosensor by differential pulse voltammetry technique for the specific detection of KRAS mutation that uses the mismatch-specific cleavage activity of T7-Endonuclease I (T7EI) coupled with horseradish peroxidase (HRP) to catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) substrate in the presence of hydrogen peroxide (H2O2). In addition, we synthesized the nanocomposite composed of multi-walled carbon nanotube/chitosan-ionic liquid/gold nanoparticles (MWCNT/Chit-IL/AuNPs) on screen-printed carbon electrode surface to increase the electrode surface area and electrochemical signal. In principle, T7E1 enzyme recognized and cleaved the mismatched site formed by the presence of KRAS gene mutation, removing 5'-biotin of capture probes and subsequently reducing the differential pulse voltammetry signal compared to wild-type KRAS gene. With this proposed strategy, a limit of detection of 11.89 fM was achieved with a broad linear relationship from 100 fM to 1 µM and discriminated 0.1% of mutant genes from the wild-type target genes. This confirms that the developed biosensor is a potential platform for the detection of mutations in early disease diagnosis.