Search Results (156)

The detection of glucose concentration has a wide range of applications and plays a significant role in the fields of the food industry, medical health, and illness diagnostics. The utilization of sensor technology for glucose concentration detection is an effective approach. Glucose sensors utilizing nanomaterials, with high sensitivity, strong resistance to interference, and compact size, exhibit tremendous potential in glucose concentration detection. Traditional enzyme-based sensors exhibit superior selectivity and high sensitivity; however, they are deficient in terms of interference resistance capabilities. With the development of nanotechnology, the performance of glucose sensors has been significantly improved. This review discusses the research progress in non-enzymatic electrochemical glucose nanosensors, including noble metal-based glucose sensors and non-noble transition metal compound-based glucose sensors, as well as the applications of multimetallic materials in nanosensors. Additionally, the application of nanosensors based on fluorescence and colorimetric principles in the detection of glucose concentration is introduced in this review. Finally, a perspective on the challenges and prospects of nanosensors in the field of glucose detection is presented. Full article

The increasing prevalence of diabetes mellitus necessitates the development of advanced glucose-monitoring systems that are non-invasive, reliable, and capable of real-time analysis. Wearable electrochemical biosensors have emerged as promising tools for continuous glucose monitoring (CGM), particularly through sweat-based platforms. This review highlights recent advancements in enzymatic and non-enzymatic wearable biosensors, with a specific focus on the pivotal role of nanomaterials in enhancing sensor performance. In enzymatic sensors, nanomaterials serve as high-surface-area supports for glucose oxidase (GOx) immobilization and facilitate direct electron transfer (DET), thereby improving sensitivity, selectivity, and miniaturization. Meanwhile, non-enzymatic sensors leverage metal and metal oxide nanostructures as catalytic sites to mimic enzymatic activity, offering improved stability and durability. Both categories benefit from the integration of carbon-based materials, metal nanoparticles, conductive polymers, and hybrid composites, enabling the development of flexible, skin-compatible biosensing systems with wireless communication capabilities. The review critically evaluates sensor performance parameters, including sensitivity, limit of detection, and linear range. Finally, current limitations and future perspectives are discussed. These include the development of multifunctional sensors, closed-loop therapeutic systems, and strategies for enhancing the stability and cost-efficiency of biosensors for broader clinical adoption. Full article

Creatinine serves as a crucial diagnostic biomarker for assessing kidney disease. This work developed portable non-enzymatic and multienzyme-modified electrochemical biosensors for the detection of creatinine based on commercial screen-printed carbon electrodes (SPCEs). The non-enzymatic creatinine sensor was constructed by the electrochemical deposition of AuNPs onto the surface of a pre-activated SPCE by electrochemical activation, followed by the surface modification of a Nafion membrane. The developed AuNPs/SCPE exhibited excellent reproducibility, and the proposed Nafion/AuNPs/SPCE sensor showed excellent detection sensitivity and selectivity toward creatinine. In comparison, the enzymatic creatinine biosensor was gradually established by the electrodeposition of a Prussian blue (PB) membrane on the optimal AuNPs/SCPE surface, followed by multi-enzyme cascade modification (which consisted of creatinine amidohydrolase (CA), creatine oxidase (CI) and sarcosine oxidase (SOx)) and drop-casting the Nafion membrane to stabilize the interface. The introduction of a PB interlayer acted as the redox layer to monitor the generation of hydrogen peroxide (H₂O₂) produced by the enzymatic reaction, while the Nafion membrane enhanced the detection selectivity toward creatine, and the multi-enzyme cascade modification further increased the detection specificity. Both non-enzymatic and enzymatic creatinine sensors could detect the lowest concentrations of less than or equal to 10 μM. In addition, the efficiency and reproducibility of the proposed composite biosensor were also confirmed by repetitive electrochemical measurements in human serum, which showed a positive linear calibration relation of peak currents versus the logarithm of the concentration between 10 μM and 1000 μM, namely, i_p (μA) = −7.06 lgC (μM) −5.30, R² = 0.996. This work offers a simple and feasible approach to the development of enzymatic and non-enzymatic creatinine biosensors. Full article

We are reporting the development of a high-performance, non-enzymatic electrochemical biosensor for selective lactate detection, integrating laser-induced graphene (LIG), gold nanoparticles (AuNPs), and a molecularly imprinted polymer (MIP) synthesized from poly(3,4-ethylenedioxythiophene) (PEDOT). The LIG electrode offers a highly porous, conductive scaffold, while electrodeposited AuNPs enhance catalytic activity and signal amplification. The PEDOT-based MIP layer, electropolymerized via cyclic voltammetry, imparts molecular specificity by creating lactate-specific binding sites. Cyclic voltammetry confirmed successful molecular imprinting and enhanced interfacial electron transfer. The resulting LIG/AuNPs/MIP biosensor demonstrated a wide linear detection range from 0.1 µM to 2500 µM, with a sensitivity of 22.42 µA/log(µM) and a low limit of detection (0.035 µM). The sensor showed excellent selectivity against common electroactive interferents such as glucose and uric acid, long-term stability, and accurate recovery in artificial saliva (>95.7%), indicating strong potential for practical application. This enzyme-free platform offers a robust and scalable strategy for continuous lactate monitoring, particularly suited for wearable devices in sports performance monitoring and critical care diagnostics. Full article

The growing global burden of diabetes necessitates the development of glucose sensors that are not only reliable and sensitive but also cost-effective and amenable to point-of-care use. In this work, we report a non-enzymatic electrochemical glucose sensor based on laser-induced graphene (LIG), functionalized with zinc oxide (ZnO) and palladium (Pd) nanostructures. The ZnO nanostructures were systematically optimized on the LIG surface by varying electrochemical deposition parameters, including applied potential, temperature, and deposition time, to enhance the electrocatalytic oxidation of glucose in alkaline medium. Subsequent modification with Pd nanostructures further improved the electrocatalytic activity and sensitivity of the sensor. The performance of the LIG/ZnO/Pd sensor was investigated using chronoamperometric and cyclic voltammetric analysis in 0.1 M NaOH at an applied potential of 0.65 V. The sensor exhibited a wide dynamic range (2–10 mM; 10–24 mM) with a limit of detection of 130 μM, capturing hypo- and hyperglycemia conditions. Moreover, a sensitivity of 25.63 µA·mM⁻¹·cm⁻² was observed. Additionally, the sensor showcased selective response towards glucose in the presence of common interferents. These findings highlight the potential of the LIG/ZnO/Pd platform for integration into next-generation, non-enzymatic glucose monitoring systems for clinical and point-of-care applications. Full article

Urea level determination in biological fluids provides nutritional information regarding the body metabolism and/or the renal condition. In order to propose a rapid determination of this biomarker at low levels in biological fluid samples, the present work developed an electrochemical sensor based on a simple arrangement of a nickel-nanoparticle-modified glassy carbon electrode (GCE/NiNPs). Under optimal conditions for selective urea detection, a linear response was obtained in the range of 0.085 to 3.10 mmol L⁻¹ (R = 0.9993), with a limit of detection of 60.0 µmol L⁻¹ and limit of quantification of 198.0 µmol L⁻¹. The GCE/NiNPs sensor showed recovery rates from samples from 105 ± 0.2% (hemodialysis wastewater) to 111 ± 0.3% (dialysate) for urea determination in biological fluid samples. The results obtained showed that the proposed method is relatively easy to operate and has a good degree of reliability and the satisfactory sensitivity required for monitoring urea, as well as exhibiting excellent detection capacity in the presence of possible interferents in both samples. Full article

We demonstrate a flexible electrochemical biosensor for non-enzymatic glucose detection under different bending conditions. The novel flexible glucose sensor consists of a Cu nanoparticle (NP)/laser-induced graphene fiber (LIGF)/porous laser-induced graphene (LIG) network structure on a polyimide film. The bare LIGF/LIG electrode fabricated using an 8.9 W laser power shows a measured sheet resistance and thickness of 6.8 Ω/□ and ~420 μm, respectively. In addition, a conventional Cu NP electroplating method is used to fabricate a Cu/LIGF/LIG electrode-based glucose sensor that shows excellent glucose detection characteristics, including a sensitivity of 1438.8 µA/mM∙cm², a limit of detection (LOD) of 124 nM, and a broad linear range at an applied potential of +600 mV. Significantly, the Cu/LIGF/LIG electrode-based glucose sensor exhibits a relatively high sensitivity, low LOD, good linear detection range, and long-term stability at bending angles of 0°, 45°, 90°, 135°, and 180°. Full article

In this study, an electrochemical non-enzymatic glucose sensor based on cobalt oxide was developed using a simple chemical bath deposition method. The as-synthesized material exhibited no significant sensitivity; the latter emerged only after subsequent electrochemical activation. To the best of our knowledge, this is the first report demonstrating the successful application of electrochemical activation to achieve enhanced sensitivity. An X-ray diffraction analysis confirmed that a single-phase Co₂(OH)₂(CO₃) material was obtained immediately after synthesis, which was subsequently transformed into Co₃O₄ nanoparticles during electrochemical activation. SEM and TEM analyses revealed that the synthesized particles initially exhibited a nanorod structure, which evolved into a highly dispersed form after activation. The non-enzymatic glucose sensor based on the electrochemically activated material demonstrated excellent glucose sensitivity of 33,245 µA mM⁻¹ cm⁻² within the linear range of 0–0.5 mM, with a detection limit (LOD) of 5 µM. The starting material remained stable for over 12 months under ambient storage conditions and regained its high sensitivity following electrochemical activation. Full article

This study explores the development of a non-enzymatic electrochemical glucose sensor based on poly(3-aminobenzoic acid) (P3ABA) combined with silver nanoparticles (AgNPs). Incorporating AgNPs into the P3ABA matrix enhances the sensor’s electrocatalytic properties, leading to a system with greater stability. Cyclic voltammetry and chronoamperometry were employed to evaluate the sensor’s performance, demonstrating a sensitivity of 50.71 µA mM⁻¹ cm⁻² and a limit of detection (LOD) of 0.2 µM. The sensor exhibited a linear response over a broad concentration range (1 to 16 mM), with a coefficient of determination (R²) of 0.998, indicating good reproducibility and precision. These results highlight the potential of the P3ABA/AgNP composite for glucose sensing applications, offering an extended linear range, allowing for the quantification of glucose concentrations from very low to significantly high levels, covering both physiological and pathological conditions. Full article

Freestanding electrode designs, cost-effective catalysts, and enhanced electrical conductivity are crucial for improving the performance of fourth-generation non-enzymatic glucose electrochemical sensors. These factors enable more efficient, scalable, and durable sensors with better sensitivity, stability, and affordability for real-time glucose monitoring. In this study, we explore a freestanding electrode design combining carbon nanotubes (CNTs) with MnO₂ nanorods to enhance charge transfer, increase surface area, and optimize catalytic activity. This CNTs/MnO₂ electrode demonstrates exceptional catalytic activity for glucose oxidation, achieving a high sensitivity of 309.73 µA cm⁻² mM⁻¹ within a linear range of 0.5 to 10 mM—well above typical physiological glucose levels (3–8 mM), with a detection limit of 0.19 mM at a signal-to-noise ratio of 3. The electrode also shows excellent durability and remarkable selectivity for glucose over common interferents like ascorbic acid and uric acid, as well as antifouling properties in the presence of KCl. These attributes are essential for accurate glucose detection in complex biological samples. The integration of MnO₂ nanorods with CNTs in freestanding nanostructures opens up exciting opportunities for developing high-performance, robust electrochemical sensors for diverse applications. Full article

The development of micro glucose sensors plays a vital role in the management and monitoring of diabetes, facilitating real-time tracking of blood glucose levels. In this paper, we developed a three-layer core-sheath microwire (NW@CuO@Co₃O₄) with nickel wire as the core and copper oxide and cobalt oxide nanowires as the sheath. The unique core-sheath structure of microwire enables it to have both good conductivity and excellent electrochemical catalytic activity when used as an electrode for glucose detecting. The non-enzymatic glucose sensor base on a NW@CuO@Co₃O₄ core-sheath wire exhibits a high sensitivity of 4053.1 μA mM⁻¹ cm⁻², a low detection limit 0.89 μM, and a short response time of less than 2 s. Full article

A novel material composed of Au@SiO₂-(3-Aminopropyl Triethoxysilane) (Au@SiO₂-APTES) was successfully synthesised using the sol–gel method, and was used to modify glassy carbon electrodes. Its effectiveness as a molecular recognition element is evaluated in the design of an electrochemical sensor for the precise detection of dopamine. The Au@SiO₂-APTES composite was analysed using Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray diffraction. Elemental analysis verified the presence of oxygen, silicon, and gold, with atomic percentages of around 77.19%, 21.12%, and 1.65%, respectively. The corresponding elemental mapping for Au@SiO₂-APTES composite showed that the spatial distribution of all the elements was fairly homogeneous throughout the composite, indicating that the Au NPs are embedded in the silica structures. Traces of dopamine were detected by differential pulse voltammetry with a low limit of detection (S/N = 3) and quantification (S/N = 10) of 1.4 × 10⁻⁸ molL⁻¹ and 4.7 × 10⁻⁸ molL⁻¹, respectively. The Au@SiO₂-APTES composite had two linear ranges: from 4.7 × 10⁻⁸ to 1 × 10⁻⁷ molL⁻¹ and 1.25 × 10⁻⁷ to 8.75 × 10⁻⁷ molL⁻¹. Moreover, the sensor showed outstanding selectivity even in the presence of various potential interfering species. It also demonstrated good reusability and signal recovery when tested in human urine and plasma samples spiked with different dopamine concentrations. The electrochemical sensor, constructed using this novel composite material, shows great promise in the selective and sensitive detection of dopamine in the biological matrix. These results underscore the sensor’s capability for practical application in analysing real-world samples. Full article

Electrochemical glucose sensors are vital for clinical diagnostics and the food industry, where accurate detection is essential. However, the limitations of glucose oxidase (GOx)-based sensors, such as complex preparation, high cost, and environmental sensitivity, highlight the need for non-enzymatic sensors that directly oxidize glucose at the electrode surface. In this study, a self-supporting hierarchical Cu/Fe₃O₄ nanosheet electrode was successfully fabricated by in situ growth on Ni Foam using a hydrothermal method, followed by annealing treatment. The Cu/Fe₃O₄ hierarchical nanosheet structure, with its large surface area, provides abundant active sites for electrocatalysis, while the strong interactions between Cu/Fe₃O₄ and Ni Foam enhance electron transfer efficiency. This novel electrode structure demonstrates exceptional electrochemical performance for non-enzymatic glucose sensing, with an ultrahigh sensitivity of 12.85 μA·μM⁻¹·cm⁻², a low detection limit of 0.71 μM, and a linear range extending up to 1 mM. Moreover, the Cu/Fe₃O₄/NF electrode exhibits excellent stability, a rapid response (~3 s), and good selectivity against interfering substances such as uric acid, ascorbic acid, H₂O₂, urea, and KCl. It also shows strong reliability in analyzing human serum samples. Therefore, Cu/Fe₃O₄/NF holds great promise as a non-enzymatic glucose sensor, and this work offers a valuable strategy for the design of advanced electrochemical electrodes. Full article

Lactate is a key metabolite in cellular respiration, and elevated levels usually indicate tissue hypoxia or metabolic dysregulation. The real-time detection of lactate levels is particularly important in situations such as exercise, shock, severe trauma, and tissue injury. Conventional lactate assays are insufficient to address today’s complex and variable testing environments, and thus, there is an urgent need for highly sensitive biosensors. This review article provides an overview of the concept and composition of electrochemical lactate biosensors, as well as their recent advances. Comparisons of popular studies on enzymatic and non-enzymatic lactate sensors, the surface-related materials used for modifications to electrochemical lactate biosensors, and the detection methods commonly used for sensors are discussed separately. In addition, advances in implantable and non-implantable miniaturized lactate sensors are discussed, emphasizing their application for continuous real-time monitoring. Despite their potential, challenges such as non-specific binding, biomaterial interference, and biorecognition element stability issues remain during practical applications. Future research should aim to improve sensor design, biocompatibility, and integration with advanced signal processing techniques. With continued innovation, lactate sensors are expected to revolutionize personalized medicine, helping clinicians to increase treatment efficiency and improve the experience of their use. Full article

With the sudden advancement of glucose biosensors for monitoring blood glucose levels for the prevention and diagnosis of diabetes, non-enzymatic glucose sensors have aroused great interest owing to their sensitivity, stability, and economy. Recently, researchers have dedicated themselves to developing non-enzymatic electrochemical glucose sensors for the rapid, convenient, and sensitive determination of glucose. However, it is desirable to explore economic and effective nanomaterials with a high non-enzymatic catalysis performance toward glucose to modify electrodes. Metal oxides (MOs) and metal sulfides (MSs) have attracted extensive interest among scholars owing to their excellent catalytic activity, good biocompatibility, low cost, simple synthesis process, and controllable morphology and structure. Nonetheless, the exploitation of MOs and MSs in non-enzymatic electrochemical glucose sensors still suffers from relatively low conductivity and biocompatibility. Therefore, it is of significance to integrate MOs and MSs with metal/carbon/conducive polymers to modify electrodes for compensating the aforementioned deficiency. This review introduces the recent developments in non-enzymatic electrochemical glucose sensors based on MOs and MSs, focusing on their preparation methods and how their structural composition influences sensing performance. Finally, this review discusses the prospects and challenges of non-enzymatic electrochemical glucose sensors. Full article