Non-enzymatic Glucose Biosensor Research Articles

Fabrication and Potential Characterization of Silver‐Doped Zinc Oxide Glucose Biosensor

This work is devoted to studying and manufacturing a highly sensitive nonenzymatic glucose biosensing system of metal oxides via the sol–gel technique. The X‐ray diffraction patterns of all the prepared samples confirm that the samples present hexagonal crystal lattice structures of ZnO and Ag–ZnO nanoparticles. Ultraviolet (UV) analysis of all the samples is carried out to evaluate the absorption of silver in the UV region for electrical and chronoamperometric analysis. The transmittance of all the samples is observed, and the maximum transmittance is 11% for 4% AgZnO. Fourier transform infrared spectroscopy reveal the functional group stretching and vibration of the particles at different wavelength ranges. Scanning electron microsocpy analysis reveals the grain size and morphology of the samples, which decrease with increasing doping agent. Chronoamperometric analysis of all the samples reveals that the value increases with time for the 4% doped sample. The sensing response is also observed and is enhanced with increasing temperature for the 4% doped sample. The sensing response of the samples coated with carbon fiber electrodes is assessed from −0.2 to +0.5 V at a scan rate of 50 mV s−1.

Study on the performance of MoS2/Au composites for non-enzymatic electrochemical glucose detection

Abstract Glucose concentration is considered an indicator for the diagnosis of diabetes, highlighting the importance of accurate glucose detection. Non-enzymatic electrochemical sensors have been extensively studied for glucose detection applications, with nanocomposites composed of molybdenum disulfide (MoS2) and gold nanoparticles (Au NPs) demonstrating high catalytic activity. In this study, a nanocomposite material composed of MoS2 and Au NPs (MoS2/Au) was synthesized and employed to construct a non-enzymatic electrochemical glucose biosensor. The detection limit of this sensor was explored, reaching as low as 1 mM. Additionally, compared to MoS2, the MoS2/Au nanocomposite exhibited a higher linear correlation coefficient and sensitivity, with a linear range of 1–25 mM and a sensitivity of 417.556 μA mM−1 cm−2. The sensor demonstrated excellent performance within the range of human blood glucose concentrations, showing potential for real-time monitoring and precise measurement of glucose levels. Furthermore, it exhibited good stability and reproducibility. These findings indicate the potential applications of MoS2/Au in biosensors and immunoassays.

Electrochemical non-enzymatic glucose biosensors based on Au-thiol-linked molecular architectures

In this work, an electrochemical non-enzymatic glucose sensor consisting of di-methanethiol-grafted poly (3,4-propylenedioxythiophene), gold nanoparticles (Au NPs), and reduced graphene oxide (rGO) was synthesized by a one-step method through Au-S chemisorption. The structure and morphology of the as-prepared poly (ProDOT-(MeSH)2)/Au/rGO composite were characterized by FT-IR, XRD, EDX, TEM, SEM, and XPS, and the electrochemical performance of the composite was investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) on glassy carbon electrode (GCE). The results show that because of the hydrogen bond interaction between the thiol group on the polymer units and the functional groups on GO, poly (ProDOT-(MeSH)2)/Au/rGO was successfully prepared. In addition, due to the unique morphological structure of the composite and the ability to absorb glucose molecules through hydrogen bonds, the poly(ProDOT-(MeSH)2)/Au/rGO electrode possesses excellent selectivity and unique sensitivity (46.13 μA mM−1 cm−2) for sensing glucose in the linear range of 0.04–16.0 mM with a detection limit of (S/N = 3) 0.01. This paper demonstrates that the poly(ProDOT-(MeSH)2)/Au/rGO composite holds great promise for application as a new glucose sensor in life science.

Enhanced Nonenzymatic Glucose Biosensor of ZnO Nanostructure via Nonthermal Plasma

The sensitive nonenzymatic sensing of glucose has been made feasible for the first time using a nonthermal plasma (NTP)-synthesized ZnO nanostructure. This work presents an interesting and novel method for surface modification. The effects of flow gas of Argon/Oxygen (20, 30 and 40 l/min) on the Zn foil surface and various properties were investigated. Optical emission spectroscopy OES has been used to characterize transmissions for positive and negative systems of Ar/O plasma. X-ray diffraction showed close adjacent tops and the strongest peak at Zn (101). EDX displays the constants (Ok_[Formula: see text], (Znk_[Formula: see text] and (Znk_[Formula: see text] and change in (ZnL_[Formula: see text]. Photoluminescence (PL) Analysis shows a shift at the vertex toward the left and then toward the right confirming the reaction of all PL spectra within a strong UV emission peak. Raman spectroscopy analysis demonstrates two clear peaks gradually shifting to the right with an increase in the percentage of gas flowing compared to the blank metal, and scanning electron microscopy (FE-SEM) images show changes in the shape of nanoparticles due to increasing gas flow, the surface of zinc metal is affected by cold plasma and forms particles with very small diameters ranging from 10.8[Formula: see text]nm to 123[Formula: see text]nm. Also altered the surface morphology where the nano shape changed from flower-like particles to sheets with diameters ranging 282.7–643.5[Formula: see text]nm and the sheets grew with the increase of gas flow to diameters ranging 132–710[Formula: see text]nm. ZnO nanostructures are employed as biosensor electrodes (nonenzymatic) glucose as the increase in current is proportional to the flowing gas (2.06E-03[Formula: see text]mA, 2.09E-03[Formula: see text]mA and 4.34E-03[Formula: see text]mA).

Growth of WO3 nanostructure deposited on TiO2 nanotube arrays for electrochemical enzyme-free glucose sensor

In this study, a novel WO3-TiO2 hybrid nanostructure-based electrochemical non-enzymatic glucose biosensor has been developed. The anodization method was utilized to successfully produce TiO2 nanotubes on Ti6Al4V alloy functioning as substrates and WO3 nanomaterial decorate on the surface of TiO2 nanotubes (TNTs) deposited through electrochemical technique. The incorporation of WO3 on TNTs has resulted in a high electroactive surface and more degradation resistance in comparison to pure TNTs, resulting in enhanced electron transfer rate and electrode stability. High-resolution transmission electron microscopy (HR-TEM), field emission scanning electron microscopy (FE-SEM), and X-ray diffraction were used to investigate the crystalline structure and morphology of the WO3-TiO2 nanostructure. The electrochemical properties of the hybrid electrodes were investigated employing amperometry, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The hybrid electrode had a promising sensitivity (1228.12 μA/mM/cm2), low detection limit (0.19 mM), wide linear range (1.0–6.5 mM), and short response time (2-s). The sensors also demonstrated superior levels of reproducibility, repeatability, and stability.

PH-Dependent Morphology of Copper (II) Oxide in Hydrothermal Process and Their Photoelectrochemical Application for Non-Enzymatic Glucose Biosensor

In this study, we investigated the influence of pH on the hydrothermal synthesis of copper (II) oxide CuO nanostructures with the aim of tuning their morphology. By varying the pH of the reaction medium, we successfully produced CuO nanostructures with three distinct morphologies including nanoparticles, nanorods, and nanosheets according to the pH levels of 4, 7, and 12, respectively. The observed variations in surface morphology are attributed to fluctuations in growth rates across different crystal facets, which are influenced by the presence of intermediate species within the reaction. This report also compared the structural and optical properties of the synthesized CuO nanostructures and explored their potential for photoelectrochemical glucose sensing. Notably, CuO nanoparticles and nanorods displayed exceptional performance with calculated limits of detection of 0.69 nM and 0.61 nM, respectively. Both of these morphologies exhibited a linear response to glucose within their corresponding concentration ranges (3–20 nM and 20–150 nM). As a result, CuO nanorods appear to be a more favorable photoelectrochemical sensing method because of the large surface area as well as the lowest solution resistance in electroimpedance analysis compared to CuO nanoparticles and nanosheets forms. These findings strongly suggest the promising application of hydrothermal-synthesized CuO nanostructures for ultrasensitive photoelectrochemical glucose biosensors.

MOF-derived NiCo hydroxide for highly efficient non-enzymatic glucose biosensing

An efficient and robust electrocatalyst is significant for glucose biosensing. The emergence of metal–organic framework (MOF) derived materials opens up new avenues for the development of high-performance glucose sensing catalysts. Herein, MOF derived nickel-cobalt hydroxide supported on conductive copper sheet (NiCo-OH/Cu sheet) is prepared at room temperature. The as-obtained NiCo-OH is endowed with three-dimensional network structure which enables the effective exposure of active materials, sufficient contact between glucose molecule and catalyst. The NiCo-OH/Cu sheet is revealed as good glucose electrochemical sensing material with a wide linear range of 0.05∼6.0 mM and a high sensitivity of 1340 μA mM−1 cm−2. Additionally, the as-fabricated NiCo-OH/Cu sheet displays good anti-interference ability and long-term stability.

Highly Efficient Non-Enzymatic Electrochemical Glucose Biosensor Based on Copper Metal Organic Framework Coated on Graphite Sheet

Detection of glucose is highly informative, creating a constant demand for fabricating high-precision glucose biosensors. Metal–organic frameworks, a family of porous materials renowned for their tunability, can be an excellent choice for developing such sensors. We have developed a highly-sensitive, non-enzymatic sensor for electrochemical detection of glucose fabricated using Copper Metal–Organic Framework (Cu MOF), synthesized by a simple, room-temperature stirring method using Benzene-1,3,5-tricarboxylic acid (BTC) as ligand and Copper nitrate trihydrate as precursor. The synthesized nanostructure was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray analytical techniques. Powder X-ray diffraction study and thermogravimetric analysis were also done. Further, Brunnauer-Emmett-Teller analysis revealed the porous nature of Cu MOF. The materials exhibited strong electro-catalytic activity for glucose oxidation as revealed from cyclic voltammetry and chronoamperometric studies done under alkaline pH conditions. The Cu MOF deposited on a conducting graphite sheet electrode displayed a significantly low detection limit of 0.019 mM through a broad detection range (1–15 mM) and a strong sensitivity of 229.4 μAmM−1 cm2. Overall, the Cu MOF/GS exhibits exceptional stability, short response time (less than 1 s), and good repeatability and reproducibility, making it a promising future material for non-enzymatic glucose detection.

Bamboo-derived activated carbon-functionalized ZnO NPs for non-enzymatic glucose sensing

Recently, bamboo activated carbon (BAC) attracted the researchers with considerable attention and as electrode material for biosensor application, due to its high surface to volume ratio, low cost, easy of synthesis, good stability, and better profit in the matter of commercialization. The present work report the synthesis of bamboo activated carbon and functionalization of bamboo carbon with ZnO nanoparticles through the green approached method with different weight ratios for non-enzymatic glucose biosensing. Moreover, bamboo leaves work as a capping and stabilizing agent for the functionalization of activated carbon. As synthesized BAC, biosynthesized ZnO and BAC functionalized ZnO NPs with different ratios of ZnO/BAC1wt%, ZnO/BAC 2 wt% and ZnO/BAC 3 wt% were analyzed with nano-characterization tools such as XRD, FTIR, UV–Visible spectroscopy, FESEM, EDX analysis, TEM. As fabricated modified electrodes ZnO/BAC 2 wt% showed better conductivity followed by ZnO/BAC 3 wt% and ZnO/BAC1wt%. Moreover, the electrochemical performance of the modified ZnO/BAC 2 wt% /Screen printed gold electrode (SPCE) exhibited good catalytic nature towards the enzyme-free glucose oxidation and the results showed an excellent sensitivity of 5048.61 μA mM−1 Cm−2, the limit of detection 0.40 μM with linearity of 1–2 mM with better stability and repeatability. This proves that a fabricated ZnO/BAC 2 wt% /SPCE sensor will be a cost-effective biosensor.

Synthesis of CuSe/PVP/GO and CuSe/MWCNTs for their applications as nonenzymatic electrochemical glucose biosensors.

Copper selenide (CuSe) is an inorganic binary compound which exhibits metallic behavior with zero band gap. CuSe has multiple applications in electrocatalysis, photothermal therapy, flexible electronic and solar cells. In the current study, copper selenide based nanocomposites CuSe/PVP/GO and CuSe/MWCNTs were synthesized by using the sol-gel method for application as a non-enzymatic glucose biosensor. Different characterization methods were employed, such as X-ray diffraction (XRD), photoluminescence (PL), Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible (UV-Vis) spectroscopy, and photoluminescence for determining various aspects of CuSe/PVP/GO and CuSe/MWCNTs nanocomposites including phase formation, functional group analysis, band gaps and morphology. Electrochemical impedance spectroscopy (EIS) showed that the resistances of modified electrode/bare electrode were 12.3 kΩ/17.3 kΩ and 6.3 kΩ/17.3 kΩ for CuSe/PVP/GO and CuSe/MWCNTs nanocomposites, respectively. Cyclic voltammetry showed that both CuSe/PVP/GO and CuSe/MWCNTs nanocomposites are promising biosensors for detection and monitoring of the glucose level in an analyte. The sensitivity and limit of detection are 2328 μA mM-1 cm-2/0.2 μM and 4157 μA mM-1 cm-2/0.3 μM for CuSe/PVP/GO and CuSe/MWCNTs, respectively. Chronoamperometry confirmed that our nanocomposite was the best sensor for glucose even in the presence of other interferents like ascorbic acid (AA), uric acid (UA) and dopamine (DA).

Correction: Synthesis of CuSe/PVP/GO and CuSe/MWCNTs for their applications as nonenzymatic electrochemical glucose biosensors

Correction for ‘Synthesis of CuSe/PVP/GO and CuSe/MWCNTs for their applications as nonenzymatic electrochemical glucose biosensors’ by Junaid Yaseen et al., RSC Adv., 2024, 14, 6896–6905, https://doi.org/10.1039/D3RA06713K.

Ni@TiO2 nanoribbon array electrode for high-efficiency non-enzymatic glucose biosensing.

The exploration of noble metal-free nanoarrays as high-activity catalytic electrodes for glucose biosensing holds great significance. Herein, we propose a Ni nanoparticle-decorated TiO2 nanoribbon array on a titanium plate (Ni@TiO2/TP) as an effective non-enzymatic glucose biosensing electrode. The as-prepared Ni@TiO2/TP electrode demonstrates rapid glucose response, a wide linear response range (1 μM to 1 mM), a low detection limit (0.08 μM, S/N = 3), and high sensitivity (10 060 and 3940 μA mM-1 cm-2), with good mechanical flexibility and stability. Moreover, it proves efficient in glucose biosensing in real human blood serum and cell culture fluid. Thus, it is highly promising for practical applications.

Investigation of Glucose Sensing via Controlled Copper Concentration in CuO for Non-Enzymatic Glucose Biosensor

Non-enzymatic glucose sensors have emerged as pivotal tools for monitoring blood glucose levels, offering advantages over traditional enzymatic methods in terms of sensitivity, selectivity, and cost-effectiveness. This study explores the utilization of a simple and low-cost method for preparation of copper oxide (CuO) nanostructures to look for the non-enzymatic glucose sensing. Morphological and structural analysis via Scanning Electron Microscopy and X-ray diffraction of synthesized CuO nanostructures revealed nearly same size, shape, and a pure monoclinic crystal structure. Fourier transform infrared spectroscopy further confirmed the monoclinic phase. More importantly, we employed CuO nanostructures-modified glassy carbon electrodes (GCE) to investigate the glucose sensing and sensing parameters. The electrodes exhibited comparable sensitivity, selectivity, and an extended dynamic range 0.4–0.6 V applied potentials with regard to earlier reports. Amperometric responses of lower concentration based synthesized CuO sample recorded at 0.5 V unveiled a low limit of detection of 5.9 μM, a sensitivity of approximately 10.6 μA/(mM·cm2), and a rapid 2 s response time. Manipulating the CuO-nanostructures and integrating on the GCE can offer a promising opportunity for enhanced non-enzymatic glucose sensing with high sensitivity, selectivity, and broad dynamic range towards utility in real-time glucose monitoring, contributing to improved healthcare diagnostics and diabetes management.

A sensitive non-enzymatic dual-conductive biosensor for continuous glucose monitoring

BackgroundDiabetes and diabetic wound management have always been urgent issues for global healthcare. In the demand for blood glucose monitoring and wound management, phenylboronic acid (PBA)-based glucose biosensors are effective assistance due to their excellent glucose specificity, high sensitivity, and response stability. Nevertheless, PBA-based glucose biosensors still have challenges in terms of wide linearity and large deformation requirements. Therefore, it is necessary to develop PBA-based glucose biosensors with satisfactory mechanical properties, high response sensitivity, excellent stability, and wide linearity. ResultsIn this work, a glucose-responsive PBA-based biosensor was successfully synthesized for the first time. The sensor materials exhibited excellent mechanical properties with an elongation at break reached up to 1000%, and the healing efficiency was over 90% within 30 min at 45 °C. Furthermore, the biosensor exhibited exceptional electromechanical responsiveness, stability, high sensitivity, and wide linearity due to the specificity of phenylboronic acid to glucose and the construction of a special HCNT/PEDOT:PSS dual conductive structure. In addition, the assembled biosensor displayed remarkable glucose, pH and temperature responses, exhibiting a linear response to glucose concentration range from 0.20 mM to 2.0 mM, with a sensitivity coefficient of 47.11 mA mM−1 and regression coefficient of 0.942. Moreover, the sensor materials showed satisfactory cytocompatibility, hemocompatibility, and antibacterial properties against Escherichia coli and Staphylococcus aureus. SignificanceFor the first time, a dual conductive structural glucose biosensor based on PBA-based copolymer was synthesized. In addition to excellent glucose sensitivity and response stability, the biosensor has a wide linearity range, excellent self-healing property, and satisfactory mechanical performance. As a promising substitute for non-enzymatic glucose biosensors, this new material with special structure and characteristics would also be beneficial to wound management in diabetic patients.

Electrodeposited Fabrication of CeO2 Branched-like Nanostructure Used for Nonenzymatic Glucose Biosensor

The fabrication of nonenzymatic glucose sensors is essential because of the enhancement in the selectivity and accuracy of these sensors. In this work, we used the electrodeposition approach to prepare a CeO2-based electrode for nonenzymatic glucose detection. A CeO2 branched-like nanostructure was successfully fabricated by electrodeposition on the surface of a Au substrate electrode at room temperature. The effects of cyclic voltammetry, CH3COOH content, and scan cycle number on the formation of the CeO2 branched-like nanostructure were investigated. The fabricated electrodes were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The results showed that a CeO2 branched-like nanostructure could be obtained with a CH3COOH content of 1.0 mL and a scan cycle number of 100 in a solution containing 0.015 M Ce(NO3)3, 0.01 M KCl, and 0.02 M CH3COONH4 and with a scan rate of 400 mV/s. The electrochemical characteristics of the sensor were examined by chronoamperometry and cyclic voltammetry. The results showed that the sensitivity of the sensor was 37.72 μA/mM·cm2 and the limit of detection (LOD) of the sensor was 0.093 mM. The findings in this work prove that it is feasible to fabricate CeO2-based sensors for nonenzymatic glucose detection.

Ultrasmall platinum nanoclusters densely immobilized on hairy metal organic framework for nonenzymatic glucose detection

Rational design of non-enzymatic nanomaterials that possess the similar functions to natural enzymes holds great promise in chemical and biological molecule detection. In this work, a non-enzymatic electrochemical biosensor for detection of glucose was developed based on poly(2-vinylpyridine) (P2VP) grafted UiO-66 metal organic framework decorated with ultrafine platinum nanoclusters (PtNCs). The as-fabricated UiO-66-g-P2VP/PtNCs nanocomposite was then placed on an indium tin oxide (ITO) electrode to construct non-enzymatic glucose biosensor for electrochemical detection of glucose in alkaline electrolyte. The resulting UiO-66-g-P2VP/PtNCs/ITO modified electrode showed two linear responses over glucose concentration ranging of 0.01–5 mM and 5–18 mM with a low detection limit of 2.18 μM (S/N = 3). Moreover, the UiO-66-g-P2VP/PtNCs/ITO serving as an electrochemical biosensor was successfully applied to the rapid determination of glucose in human serum sample with a desirable result. Our findings pave the way for design and development of a promising artificial enzyme for the construction of high performance sensing platform.

Inorganic Chemistry in Dalian University of Technology: Fundamental Science and Solution for Renewable Energy, Environment, Health, and Materials

Inorganic Chemistry in Dalian University of Technology: Fundamental Science and Solution for Renewable Energy, Environment, Health, and Materials

Highly efficient and sensitive non-enzymatic glucose biosensor based on flower-shaped CuO-colloid nanoparticles decorated with graphene-modified nanocomposite electrode

In this work, copper nanoparticles were synthesized through the colloidal and solution combustion method, and their electrochemical properties were evaluated using three electrode systems to detect glucose content. The solution combustion method using the fuels glycine (Gly) and hydrazine (Hyd) produces nanoparticles with amorphous spherical forms and a small flake-like structure. The colloidal method yields Cu-Colloid nanoparticles that have a homogenous phase and a flower-like structure with high electro-oxidative current due to the large surface area of the developed nanoparticle which is in contact with the glucose. A glucose biosensor was then fabricated using the developed colloidal copper nanoparticles modified with graphene-coated on indium-coated tin oxide (ITO) glass substrate (Flower shaped-CuO/G/ITO) as a working electrode. The copper nanoparticles were characterized by an X-ray diffractometer, UV–VIS spectrometer, Transmission, and Scanning electron microscope for crystalline, morphological, surface studies with 10–20 nm in diameter, 280–310 nm absorption range, and energy bandgap of 1.45ev. The lower detection limit of 1 μmol L−1, the sensitivity of 1610 μA mM−1 cm−2, and the linear range of 1 μMto μ850 M at an applied potential of +0.60 V vs. Ag/AgCl was obtained for the developed nanocomposite electrode. The developed bioelectrode shows good stability and reproducibility with less response time making it a promising electrode for developing a non-enzymatic glucose biosensor.

Molybdenum-cobalt micro-nano interface assisted ultrasensitive and selective non-enzymatic glucose biosensor

In the present work, we report highly sensitive and selective non-enzymatic glucose biosensor using novel hybrid CoOOH nanospheres decorated MoO3 nanobelts (MoCo). MoCo nanocomposite exhibits superior sensing properties toward glucose detection due to its improved electron transfer capability along with the large surface area. The biosensor achieved an excellent linear range within the concentration of 0.001–1.0 mM correspond to the amperometric current response was obtained from GCE/MoCo/Nafion electrode. The biosensing electrode is resulted a linear regression coefficient (R2 = 0.9959) and limit of detection (LOD) is 56 µM at (S/N = 3). The performance optimization of the biosensor was performed at a different operating temperature subjected to successive glucose additions. A remarkable selectivity is obtained against to the glucose at presence of different interfering substance and long-term stability of 30 days reached without a noticeable decay in the amperometric current response.

Nonenzymatic Glucose Biosensors: Latest Advances and Perspectives

Over the sixty years since glucose biosensor was introduced, development of glucose biosensor had experienced three generations. Considering the increasing demand of glucose biosensor, research and development has been carried out for more promising nonenzymatic glucose biosensor. Compared to the traditional enzyme-based glucose biosensor, nonenzymatic sensor is more capable to continuous glucose detection and has higher stability. Additionally, nonenzymatic glucose biosensor has a lower fabrication cost, which can be beneficial to the wide range of patients with the need for constant checking for blood glucose concentration. This paper introduces two proposed nonenzymatic glucose detection models: activated chemisorption and incipient hydrous oxide adatom mediator. As the developing trend of glucose biosensors is toward wearable and continuous glucose monitoring, two wearable sensors and working principles are introduced. This paper describes the application progress of different types of materials in enzyme-free blood glucose sensors, puts forward the existing problems in the application of enzyme-free blood glucose sensors, and looks forward to its future application prospects.