Search Results (304)

Narcotics trafficking is a fundamental part of organized crime, posing significant and evolving challenges for forensic investigations. Addressing these challenges requires rapid, precise, and scientifically validated analytical methods for reliable identification of illicit substances. Over the past five years, forensic drug testing has advanced considerably, improving detection of traditional drugs—such as tetrahydrocannabinol, cocaine, heroin, amphetamine-type stimulants, and lysergic acid diethylamide—as well as emerging new psychoactive substances (NPS), including synthetic cannabinoids (e.g., 5F-MDMB-PICA), cathinones (e.g., α-PVP), potent opioids (e.g., carfentanil), designer psychedelics (e.g., 25I-NBOMe), benzodiazepines (e.g., flualprazolam), and dissociatives (e.g., 3-HO-PCP). Current technologies include colorimetric assays, ambient ionization mass spectrometry, and chromatographic methods coupled with various detectors, all enhancing accuracy and precision. Vibrational spectroscopy techniques, like Raman and Fourier transform infrared spectroscopy, have become essential for non-destructive identification. Additionally, new sensors with disposable electrodes and miniaturized transducers allow ultrasensitive on-site detection of drugs and metabolites. Advanced chemometric algorithms extract maximum information from complex data, enabling faster and more reliable identifications. An important emerging trend is the adoption of green analytical methods—including direct analysis, solvent-free extraction, miniaturized instruments, and eco-friendly chromatographic processes—that reduce environmental impact without sacrificing performance. This review provides a comprehensive overview of innovations over the last five years in forensic drug analysis based on the ScienceDirect database and highlights technological trends shaping the future of forensic toxicology. Full article

This study presents a comprehensive evaluation and an equivalent circuit modeling of the skin–electrode impedance characteristics of three types of ultra-thin tattoo electrodes, all based on Parylene C nanofilms but with different active materials: Gold, Silver, and PEDOT:PSS. Their performance was compared to standard disposable Ag/AgCl electrodes. Impedance measurements were carried out on six human subjects under controlled conditions, assessing the frequency response in the range of 20 Hz to 1 kHz. For each subject, the impedance was recorded six times over one hour to investigate the stability and the temporal performance. The collected data were subsequently analyzed to model the electrical properties and interface behavior of each electrode type. The findings demonstrate that the tattoo electrodes offer impedance levels comparable to those of Ag/AgCl electrodes (in the order of tens of kΩ at 20 Hz), while providing additional benefits such as enhanced conformability, improved skin adhesion, and reduced skin irritation during use. Furthermore, the modeling of the skin–electrode interface through a more detailed equivalent circuit than the single time constant model enables a more detailed interface analysis and description, with fitting algorithm R² scores of about 0.999 and 0.979 for the impedance magnitude and impedance phase, respectively. The proposed equivalent circuit offers valuable insights for optimizing electrode design, supporting the potential of Parylene C-based tattoo electrodes as promising alternatives for next-generation wearable bioelectronic applications. Full article

In this study, a simple and effective approach was developed for the quantitative detection of serotonin. Hexagonal copper selenide nanostructures (CuSe) were employed to modify a disposable screen-printed carbon electrode (SPCE), and their ability to electrochemically detect serotonin in serum samples was investigated. The fabricated CuSe nanostructures exhibited an interconnected, cluster-like morphology composed of irregularly shaped particles with a distinct hexagonal crystal structure. The electrochemical results revealed that the CuSe/SPCE sensor showed better electrochemical activity and good analytical sensing performance towards serotonin detection. The sensor exhibited a linear response in the concentration range of 10 to 1000 nM, with an excellent correlation coefficient (R² = 0.9998) and a low detection limit of 3 nM. Furthermore, the CuSe/SPCE showed better selectivity, impressive sensitivity (12.45 µM/µA cm⁻²), and good reproducibility toward serotonin detection, making it a promising electrochemical biosensor for serotonin detection in various real biological samples. Full article

The safe disposal of high-level radioactive waste (HLW) is imperative for sustaining China’s rapidly expanding nuclear power sector, with deep geological repositories requiring rigorous site evaluation via underground research laboratories (URLs). This study presents a controlled-source audio-frequency magnetotellurics (CSAMT) survey at the Xinchang site in China’s Beishan area, a region dominated by high-resistivity metamorphic rocks. To overcome electrical data acquisition challenges in such resistive terrains, salt-saturated water was applied to transmitting and receiving electrodes to enhance grounding efficiency. Using excitation frequencies of 9600 Hz to 1 Hz, the survey achieved a 1000 m investigation depth. Data processing incorporated static effect removal via low-pass filtering and smoothness-constrained 2D inversion. The results showed strong consistency between observed and modeled data, validating inversion reliability. Borehole correlations identified a 600-m-thick intact rock mass, confirming favorable geological conditions for URL construction. The study demonstrates CSAMT’s efficacy in characterizing HLW repository sites in high-resistivity environments, providing critical geophysical insights for China’s HLW disposal program. These findings advance site evaluation methodologies for deep geological repositories, though integrated multidisciplinary assessments remain essential for comprehensive site validation. This work underscores the feasibility of the Xinchang site while establishing a technical framework that is applicable to analogous challenging terrains globally. Full article

An electrochemical aptasensor was developed for the rapid and sensitive detection of ciprofloxacin (CPX) in milk samples. The device was fabricated on a polyethylene terephthalate (PET) substrate using a screen-printing technique with carbon-based conductive ink. Gold nanoparticles (AuNPs) were incorporated to enhance aptamer immobilization and facilitate electron transfer at the electrode surface. The sensor’s analytical performance was optimized by adjusting key parameters, including AuNP volume, DNA aptamer concentration, and incubation times for both the aptamer and the blocking agent (6-mercapto-1-hexanol, MCH). Differential pulse voltammetry (DPV) measurements demonstrated a linear response ranging from 10 to 50 nmol L⁻¹ and a low detection limit of 3.0 nmol L⁻¹. When applied to real milk samples, the method achieved high recovery rates (101.4–106.7%) with a relative standard deviation below 3.1%, confirming its robustness. This disposable and cost-effective aptasensor represents a promising tool for food safety monitoring, with potential for adaptation to detect other pharmaceutical residues in dairy products. Full article

Dopamine is a major catecholamine neurotransmitter that plays an essential role in the functioning of the human central nervous system. Imbalances in dopamine levels are associated with neurological disorders and depression. Thus, measuring the concentration of DA in human body fluids is significantly important. In this work, TEMPO-oxidized cellulose nanofibrils (TOCNFs) extracted from marram grass (Ammophilia arenaria), harvested in the central western part of Tunisia, were utilized to modify disposable screen-printed carbon electrodes (SPCEs) for the sensitive detection of dopamine in biological fluids. Differential pulse voltammetry (DPV) measurements displayed a sensitivity of 7.92 µA/µM and a detection limit of 10 nM. The disposable TOCNF-modified SPCE presents a charge transfer coefficient, α, comparable to that of a TOCNF/graphene/AgNP composite-modified GCE. Moreover, it exhibits good repeatability (RSD = 1.9%), good reproducibility (RSD = 2.3%), and appreciable storage stability (91% of its initial response after 3 weeks). The prepared disposable sensor showed satisfactory recovery of dopamine in human urine samples. Full article

The BRCA-1 protein, recognized for its diagnostic relevance in a wide spectrum of malignancies, has been the focus of extensive investigation. In this study, an electrochemical immunosensor specifically designed for BRCA-1 detection was fabricated. The sensing platform utilizes disposable pencil graphite electrodes modified with a nanocomposite composed of gold nanoparticles (AuNPs), molybdenum disulfide (MoS₂), and chitosan (CS). This multifunctional nanostructure significantly promotes electron transfer efficiency and supports the effective immobilization of antibodies. The constructed immunosensor exhibited excellent analytical performance, with a linear detection range between 0.05 and 20 ng/mL for BRCA-1 and a notably low limit of detection at 0.04 ng/mL. The device maintained a relative standard deviation of 3.59% (n = 3), indicating strong reproducibility. In addition, a high recovery rate of 98 ± 3% was achieved in spiked serum samples, even in the presence of common electroactive interferents such as dopamine and ascorbic acid. These findings highlight the sensor’s promising applicability for the clinical detection of BRCA-1 and potentially other cancer-related biomarkers. Full article

In this research, an interdigitated gear-shaped working electrode is presented for cortisol sensing. Overall, the sensor was designed in a three-electrode system and was fabricated using direct laser scribing. A synthesized conductive ink based on graphene and polyaniline was further employed to enhance the electrochemical performance of the sensor. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were employed for physicochemical characterization of the laser-induced graphene (LIG) sensor. Cortisol, a biomarker essential in detecting stress, was detected both in phosphate-buffered saline (PBS, pH = 7.4) and human serum within a linear range of 100 ng/mL to 100 µg/mL. Ferri/ferrocyanide was employed as the redox probe to detect cortisol in PBS. The electrochemical performance of the developed sensor was assessed via differential pulse voltammetry (DPV), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry. The electrochemical performance demonstrates high sensitivity and selectivity alongside strong repeatability (relative standard deviation (RSD) = 3.8%, n = 4) and reproducibility (RSD = 5.85%, n = 5). Overall, these results highlight the sensor’s reliability, high sensitivity, and repeatability and reproducibility in the detection of cortisol. The sensor successfully detected cortisol in the complex medium of human serum and effectively distinguished it in a ternary mixture containing cortisol and dopamine. Also, the use of direct laser writing on Kapton film makes the approach cost-effective and thus disposable, making it suitable for chronic stress diagnostics and neurological research applications. Full article

Copper-thiolate nanostructures, formed through the self-assembly of cysteine (Cys) and glutathione (GSH) with copper ions, offer a versatile platform for redox-active applications due to their structural stability and chemical functionality. In this study, Cu-Cys-GSH nanoparticles were synthesized and employed to develop a capacitive biosensor for the ultralow concentration detection of hydrogen peroxide (H₂O₂). The detection mechanism leverages a Fenton-like reaction, where H₂O₂ interacts with Cu-Cys-GSH nanoparticles to generate hydroxyl radicals (·OH) through redox cycling between Cu²⁺ and Cu⁺ ions. These redox processes induce changes in the sensor’s surface charge and dielectric properties, enabling highly sensitive capacitive sensing at gold interdigitated electrodes (IDEs). The influence of chirality on sensing performance was investigated by synthesizing nanoparticles with both L- and D-cysteine enantiomers. Comparative analysis revealed that the stereochemistry of cysteine impacts the catalytic activity and sensor response, with Cu-L-Cys-GSH nanoparticles exhibiting superior performance. Specifically, the biosensor achieved a linear detection range from 1.0 fM to 1.0 pM and demonstrated an ultra-sensitive detection limit of 21.8 aM, outperforming many existing methods for H₂O₂ detection. The sensor’s practical performance was further validated using milk and saliva samples, yielding high recovery rates and confirming its robustness and accuracy for real-world applications. This study offers a disposable, low-cost sensing platform compatible with sustainable healthcare practices and facilitates easy integration into point-of-care diagnostic systems. Full article

A voltammetric method based on the use of screen-printed carbon electrodes (SPCEs) is presented for the simultaneous determination of salbutamol (SAL), sulfamethoxazole (SMX), and trimethoprim (TMP), with high sensitivity, fast response, and excellent repeatability and reproducibility. Under the optimal voltammetric conditions, the simultaneous analysis showed linear ranges of 0.3–2.5 mg L⁻¹, 0.3–11.1 mg L⁻¹, and 0.5–9.0 mg L⁻¹ for SAL, SMX, and TMP, respectively, and detection limits of 83.8 μg L⁻¹, 88.7 μg L⁻¹, and 139.2 μg L⁻¹, respectively. Additionally, the developed method was successfully validated by the analysis of a spiked river water sample with satisfactory recovery values in the range of 97.0–98.8%. The added value of the presented method relays in combining cost-effective disposable SPCEs with rapid analysis (<30 s), providing portable electrochemical tools for the on-site monitoring of pharmaceutical residues, which is critical for addressing contamination linked to anthropogenic activity. Full article

Addressing hazards from dangerous pollutants requires specialized techniques and risk-control strategies, including detection, neutralization and disposal of contaminants. Smart polymers, designed for specific contaminants, provide powerful solutions for hazardous compound challenges. Their remarkable performance capabilities and potential applications present exciting opportunities for further exploration and development in this field. This editorial aims to provide a comprehensive overview of smart materials with unique features and emerging polymeric technologies that are being developed for isolation, screening, removal, and decontamination of hazardous compounds (e.g., heavy metals, pharmaceutically active contaminants, hormones, endocrine-disrupting chemicals, pathogens, and energetic materials). It highlights recent advancements in synthesis methods, characterization, and the applications of molecularly imprinted polymers (MIPs), along with alternative smart polymeric platforms including hydrogels, ion-imprinted composites, screen-printed electrodes, nanoparticles, and nanofibers. MIPs offer highly selective recognition properties, reusability, long-term stability, and low production costs. Various MIP types, including particles and films, are used in applications like sensing/diagnostic devices for hazardous chemicals, biochemicals, pharmaceuticals, and environmental safety. Full article

In the present work, we designed a straightforward and disposable voltammetric sensor utilizing a molybdenum disulfide/multi-walled carbon nanotube nanostructure-modified screen-printed carbon electrode (MoS₂/MWCNTs/SPCE) for 4-nitrophenol (4-NP) determination. The successful synthesis of the MoS₂/MWCNT nanostructure was characterized using Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EXD) mapping. The electrochemical behavior of 4-NP at the MoS₂/MWCNTs/SPCE was examined using differential pulse voltammetry (DPV), cyclic voltammetry (CV), and chronoamperometry techniques. The MoS₂/MWCNTs/SPCE exhibited outstanding electro-catalytic activity for the voltammetric detection of 4-NP. Under optimized conditions, the reduction peak current showed a linear dependence with the concentration of 4-NP in the range of 0.05 to 800.0 µM, and a detection limit (LOD) of 0.01 µM was determined. In addition, the MoS₂/MWCNTs/SPCE sensor has advantages including repeatability, reproducibility, stability, inexpensiveness, and practical application. The MoS₂/MWCNTs/SPCE-based sensor was also utilized for the determination of 4-NP in real water specimens. 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

The development of sensitive, selective, and reliable glucose biosensors remains a persistent challenge in clinical diagnostics. In this study, we exploited the advantageous (electro)catalytic properties of bismuth ruthenate (Bi₂Ru₂O₇) pyrochlore clusters, known for their high surface activity and metallic-like conductivity, and the favorable physicochemical properties of multi-walled carbon nanotubes (MWCNTs) by combining them with glucose oxidase (GOD) in a sensitive and selective disposable glucose biosensor. The integration of Bi₂Ru₂O₇ enabled an enhanced and more reproducible response of the biosensor along with fast and improved communication between the supporting electrode and the upper biosensing layer. The architecture of the biosensor involves the deposition of an MWCNT layer on a ferrocyanide-modified screen-printed carbon electrode (FCN-SPCE), followed by the application of a biorecognition layer including GOD and Bi₂Ru₂O₇ clusters. The voltammetric biosensor showed excellent electroanalytical performance, capable of detecting low glucose concentrations with a detection limit of 40 µM along with a linear response across the examined concentration range of 1.0–20.0 mM. The biosensor exhibited good reproducibility with a relative standard deviation (RSD) of 1.2% and interference-free operation against several of the most common interfering compounds. The practical applicability of the biosensor was demonstrated by the determination of glucose in a real serum sample spiked with different concentrations of glucose. Full article

Surface electromyography (sEMG) is increasingly important for prevention, diagnosis, and rehabilitation in healthcare. The continuous monitoring of muscle electrical activity enables the detection of abnormal events, but existing sEMG systems often rely on disposable pre-gelled electrodes that can cause skin irritation and require precise placement by trained personnel. Wearable sEMG systems integrating textile electrodes have been proposed to improve usability; however, they often suffer from poor skin–electrode coupling, leading to higher impedance, motion artifacts, and reduced signal quality. To address these limitations, we propose a preliminary model of smart socks, integrating biocompatible hybrid polymer electrodes positioned over the target muscles. Compared with commercial Ag/AgCl electrodes, these hybrid electrodes ensure lower the skin–electrode impedance, enhancing signal acquisition (19.2 ± 3.1 kΩ vs. 27.8 ± 4.5 kΩ for Ag/AgCl electrodes). Moreover, to the best of our knowledge, this is the first wearable system incorporating hydrogel-based electrodes in a sock specifically designed for the analysis of lower limb muscles, which are crucial for evaluating conditions such as sarcopenia, fall risk, and gait anomalies. The system incorporates a lightweight, wireless commercial module for data pre-processing and transmission. sEMG signals from the Gastrocnemius and Tibialis muscles were analyzed, demonstrating a strong correlation (R = 0.87) between signals acquired with the smart socks and those obtained using commercial Ag/AgCl electrodes. Future studies will further validate its long-term performance under real-world conditions and with a larger dataset. Full article