Colorimetric Detection Of Glucose Research Articles

Synthesis of a perylene diimide functionalized Sb2S3 nanocomposites and its application as a peroxidase mimic for colorimetric detection of H2O2 and glucose

N, N’-di (L-glutamic amine)-perylene-3,4,9,10-tetracarboxylic diimide (GAPDI) functionalized Sb2S3 nanocomposites (GAPDI-Sb2S3) were fabricated using a hydrothermal method and characterized. GAPDI-Sb2S3 nanocomposites can catalyze the oxidation of 3,3′,5,5′- tetramethyl benzidine (TMB) by H2O2. The experimental conditions including pH and temperature were optimized. GAPDI-Sb2S3 nanocomposites showed a strong affinity for TMB substrates, and their catalytic activity followed the Michaelis–Menten kinetics. The experimental results showed that GAPDI-Sb2S3 nanocomposites exhibited a low detection limit (LOD = 0.39 μM) and high sensitivity for H2O2 detection and showed good response to glucose detection with a LOD of 0.42 μM over arrange of 2–10 μM. These findings suggest broad application prospects in the fields of environmental chemistry, biotechnology, and biomedicine.

Sustainable Synthesis of CuO Nanoparticles for Colorimetric Detection of Hydrogen Peroxide and Glucose

Sustainable Synthesis of CuO Nanoparticles for Colorimetric Detection of Hydrogen Peroxide and Glucose

Copper oxide nanosheets as an effective nanozyme with haloperoxidase-like activity for the colorimetric detection of H2O2 and glucose

Copper oxide nanosheets (CuO NSs) have been successfully obtained by exploiting an effective one-step approach of sugar-blowing method followed by calcination. The nanosheets were characterized by several techniques like X-ray powder diffraction (XRD), Transmission electron microscopy (TEM), X-ray photoelectron Spectroscopy (XPS) and Fourier Transform Infrared Spectroscopy (FTIR). Impressively, CuO NSs display haloperoxidase (HPO) like catalytic activity which catalyses the oxidation of chloride ions by H2O2 giving rise to reactive chlorine species (RCS). A sensitive and selective colorimetric sensor was then demonstrated via the oxidation of chromogenic substrate 3,3′,5,5′- tetramethylbenzidine (TMB) by the novel nanoenzyme CuO NSs through the generation of RCS for H2O2 and glucose detection with limit of detection of 109 nM and 21 nM in the linear ranges of 4.6 µM to 769 µM and 0.22 µM to 19.57 µM respectively. Additionally, the methodology is validated for the analysis of glucose in real samples.

Fe-doped Zinc-MOF composites and its test-strip employed for colorimetric detection of glucose in model and real urine samples

A new MOF {[Zn3(Cei)2(COO)2(Bimb)3].C2H2}n(Zinc-MOF) and its Iron doped composite (Fe@Zinc-MOF) based luminescent probe is fabricated which is corroborated with various analytical techniques and employed for Glucose detection in model and real urine samples. The linear correlation coefficient for 110 and 150 mg/dl Glucose are R2 = 0.97118 and 0.97118 respectively and the calculated result of KSV at low concentration is 3.2 × 104 M−1 and 3.8 × 104 M−1 in real urine sample. The minimum detection limit is 1.17 ppm and 0.846 ppm for 110 and 150 mg/dl Glucose correspondingly in real urine sample. Furthermore, the amalgamated strip is derived from filter paper and Fe@Zinc-MOF composite which is establishing an ultra-sensitive detection relationship with noticeable fluorescence changes with respect to different concentrations of Glucose.

Smartphone-based colorimetric detection platform using color correction algorithms to reduce external interference

Smartphone-based digital image colorimetry is a powerful, fast, low-cost approach to detecting target analytes. However, lighting conditions and camera parameters easily affect the detection results, significantly curtailing its applicability in multiple scenarios. In this study, an Android-based mobile application (SMP-CC) is developed, which offers a comprehensive package that includes image acquisition, color correction, and colorimetric analysis functions. Using a custom color card, a built-in algorithm in SMP-CC can minimize the color difference between the standard color block image captured by different smartphones under different lighting conditions and the standard value by an LS171 colorimeter less than 4.36. The algorithm significantly eliminates the impacts of external lighting conditions and differences in cell phone models. Furthermore, the feasibility of SMP-CC was verified by successful colorimetric detection of urine pH, glucose, and protein, demonstrating its potential in smartphone-based digital image colorimetry.

Enhanced peroxidase-like activity of Cu–Cu2O composite film through PtPd immobilization for colorimetric glucose detection

In this study, Cu–Cu2O/PtPd nanocomposites were synthesized and characterized for their peroxidase-like enzyme activity. X-ray diffraction and energy dispersive X-ray spectroscopy analyses confirmed the successful synthesis of the nanocomposites, which exhibited a flower-like morphology and a more uniform dispersion than Cu–Cu2O. The catalytic activity of Cu–Cu2O/PtPd was evaluated using the chromogenic substrate 3,3′,5,5′-tetramethylbenzidine (TMB), finding that Cu–Cu2O/PtPd outperformed Cu–Cu2O. The optimal temperature and pH for the catalytic activity of Cu–Cu2O/PtPd were determined to be 40 °C and pH 4.0, respectively. A kinetic analysis revealed that Cu–Cu2O/PtPd followed Michaelis–Menten kinetics and exhibited a higher affinity toward TMB than the horseradish peroxidase enzyme. The catalytic mechanism of Cu–Cu2O/PtPd involved the generation of hydroxyl radicals, which facilitated the oxidation of TMB. Furthermore, the Cu–Cu2O/PtPd nanocomposite was successfully applied for the colorimetric detection of glucose, demonstrating a linear range of 8–90 μM, a detection limit of 2.389 μM, and high selectivity for glucose over other sugars.

Ultra-trace Ag doped carbon quantum dots with peroxidase-like activity for the colorimetric detection of glucose

Carbon quantum dots (CQDs) have significant applications in nanozymes. However, previous studies have not elucidated the structure–activity relationship and enzyme mechanism. In this study, we employed a one-step microwave method to synthesize ultra-trace Ag-doped carbon quantum dots (Ag-CQDs). In the presence of hydrogen peroxide (H2O2), we used the oxidative coupling reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) to evaluate the intrinsic peroxidase-like activity, kinetics, and mechanism of Ag-CQDs. The trace amount of doped Ag (1.64 %) facilitated electron transfer from the CQDs interior to the surface. The electron transfer triggered the peroxide activity of CQDs, producing hydroxyl radical (·OH), which oxidized the colorless TMB to blue-colored TMB (oxTMB). By coupling with glucose oxidase (GOx), the Ag-CQDs/H2O2/TMB system has been used for colorimetric glucose determination. The system demonstrated a low detection limit (0.17 µM), wide linear range (0.5–5.5 µM), and satisfactory results when fruit juice was analyzed. This study reports a feasible method for the colorimetric detection of glucose by synthesizing ultra-trace Ag-doped carbon quantum dots with peroxidase‐mimicking activity.

Bimetallic FeOx-TiO2@Carbon hybrid structure materials with notable peroxidase enzyme mimics applied toone-step colorimetric detection of glucose.

FeOx-TiO2@Carbon hybrid structure materials (FeOx-TiO2@CHs) with high peroxidase (POD)-like activity have been preparedby one-pot hydrothermal method. Based on the excellent POD activity of FeOx-TiO2@CHs, one pot colorimetric detection for glucose was constructed by using TMB as substrate with the synergistic reaction of glucose oxidase; the linear range and the limit of detection (LOD) are 25 ~ 1000 and 1.77µM, respectively. Using this method, the glucose in serum real samples was detected with satisfactory results, and the results are consistent with that of the glucometer method in the hospital. The recovery in diabetic and artificial urine samples was 95.71 ~ 104.67% and 99.01 ~ 103.16%, respectively. Themechanism of the catalytic colorimetric reaction was also investigated by multiple measurements, and the results indicated that superoxide anions (O2•-) between FeOx-TiO2@CHs and substrate play a main role, but a small quantity of hydroxyl radical •OH and singlet oxygen 1O2 is also generated simultaneously. The one-pot reaction method is simple and fast; the detection process only requires a simple mixing, which is suitable for application in special environment.

Ag-carbon dots with peroxidase-like activity for colorimetric and SERS dual mode detection of glucose and glutathione

Currently, nanozymes have made important research progress in the fields of catalysis, biosensing and tumor therapy, but most of nanozymes sensing systems are single-mode detection, which are easily affected by environment and operation, so it is crucial to construct nanozymes sensing system with dual-signal detection to obtain a more stable and reliable performance. In this paper, Ag-carbon dots (Ag-CDs) bifunctional nanomaterials were synthesized using carbon dots as reducing agent and protective agent by a facile and green one-step method. A simple and sensitive colorimetric-SERS dual-mode sensing platform was constructed for the detection of glucose and glutathione(GSH) in body fluids by taking advantage of good peroxidase-like and SERS activities of Ag-CDs. Ag-CDs catalyzes H2O2 to hydroxyl radicals(•OH), which oxidized TMB to form ox-TMB blue solution with characteristic absorption peak at 652 nm and Raman characteristic peak at 1607 cm−1. Ag-CDs sensing method exhibited high performance for glucose and GSH with detection limits for colorimetric and SERS as low as 11.30 μM and 3.54 μM, 0.38 μM and 0.24 μM respectively (S/N = 3). In addition, Ag-CDs have good stability and uniformity, ensuring long-term applicability of catalytic system. This colorimetric-SERS dual-mode sensing platform can be used for the determination of glucose and GSH in saliva and urine, and has the advantages of simple, low cost, rapid, and high accuracy, which has a potential application prospect in biosensor and medical research.

Multi-material 3D printed eutectogel microneedle patches integrated with fast customization and tunable drug delivery

Microneedle patches are emerging multifunctional platforms for transdermal diagnostics and drug delivery. However, it still remains challenging to develop smart microneedles integrated with customization, sensing, detection and drug delivery by 3D printing strategy. Here, we present an innovative but facile strategy to rationally design and fabricate multifunctional eutectogel microneedle (EMN) patches via multi-material 3D printing. Polymerizable deep eutectic solvents (PDES) were selected as printing inks for rapid one-step fabrication of 3D printing functional EMN patches due to fast photopolymerization rate and ultrahigh drug solubility. Moreover, stretchable EMN patches incorporating rigid needles and flexible backing layers were easily realized by changing PDES compositions of multi-material 3D printing. Meanwhile, we developed multifunctional smart multi-material EMN patches capable of performing wireless monitoring of body movements, painless colorimetric glucose detection, and controlled transdermal drug delivery. Thus, such multi-material EMN system could provide an effective platform for the painless diagnosis, detection, and therapy of a variety of diseases.

Construction of Mn-decorated zeolitic imidazolate framework-90 nanostructure as superior oxidase-like mimic for colorimetric detection of glucose and choline

A Mn decorated zeolitic imidazolate framework-90 (ZIF-90) nanozyme (Mn/ZIF-90) was constructed through an effective and rapid post-synthetic strategy for the first time. The Mn in Mn/ZIF-90 exists in mixed valence states, which is doped to the ZIF-90 through the formation of Mn–O bond. The Zn–N coordination structure of ZIF-90 may change the electronic arrangement of oxygen atoms in the free carbonyl groups (–CHO), allowing the coordination of Mn with O. The prepared Mn/ZIF-90 possesses outstanding oxidase-like activity and remarkable stability. Besides, the catalytic activity of Mn/ZIF-90 can be inhibited in the presence of H2O2. Therefore, using the Mn/ZIF-90-triggered chromogenic reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) as an amplifier, a versatile enzyme cascade-based colorimetric method for the detection of glucose and choline with good sensitivity and selectivity was developed. The linear ranges for glucose and choline are 6.25–500 μM and 5–1000 μM, respectively. Furthermore, the developed method was applied in the detection of glucose and choline in rabbit plasma samples, and the recoveries are 89.5–107.3 % and 96.0–109.3 %, respectively. In short, the simple and efficient post-synthetic doping method may provide a new thought for the rational designs of enzyme mimics with improved catalytic performance. Moreover, the colorimetric method based on the excellent catalytic activity of Mn/ZIF-90 may be extended to detect other H2O2-generating or consuming molecules and evaluate the activity of bio-enzymes that can catalyze the generation of glucose or choline.

Microwave-assisted synthesis of Limonia acidissima Groff gum stabilized palladium nanoparticles for colorimetric glucose sensing

Herein, we present a novel microwave-assisted method for the synthesis of palladium nanoparticles (PdNPs) supported by Limonia acidissima Groff tree extract gum. The synthesized PdNPs were characterized using various analytical techniques, including FTIR, SEM, TEM, UV–visible, and powder XRD analyses. TEM and XRD analysis confirmed that the synthesized LAG-PdNPs are highly crystalline nature spherical shapes with an average size diameter of 7–9 nm. We employed these gum-capped PdNPs to investigate their peroxidase-like activity for colorimetric detection of hydrogen peroxide (H2O2) and glucose. The oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) by H2O2, catalyzed by PdNPs, produces oxidation products quantified at 652 nm using spectrophotometry. The catalytic activity of PdNPs was optimized with respect to temperature and pH. The developed method exhibited a linear range of detection from 1 to 50 µm, with detection limits of 0.35 µm for H2O2 and 0.60 µm for glucose.

High-sensitivity flip chip blue Mini-LEDs miniaturized optical instrument for non-invasive glucose detection

The colorimetric detection of glucose typically involves a peroxidase reaction producing a color, which is then recorded and analyzed. However, enzyme detection has difficulties with purification and storage. In addition, replacing enzyme detection with chemical methods involves time-consuming steps such as centrifugation and purification and the optical instruments used for colorimetric detection are often bulky and not portable. In this study, ammonium metavanadate and sulfuric acid were used to prepare the detection solution instead of peroxidase to produce color. We also analyzed the effect of different concentrations of detection solution on absorbance sensitivity. Finally, a flip chip blue Mini-LEDs miniaturized optical instrument (FC blue Mini-LEDs MOI) was designed for glucose detection using optics fiber, collimating lenses, a miniaturized spectrometer, and an FC Blue Mini-LEDs with a center wavelength of 459 nm. While detecting glucose solutions in the concentration range of 0.1–10 mM by the developed MOI, the regression equation of y = 0.0941x + 0.1341, R2 of 0.9744, the limit of detection was 2.15 mM, and the limit of quantification was 7.163 mM. Furthermore, the preparation of the detection solution only takes 10 min, and the absorbance sensitivity of the optimized detection solution could be increased by 2.3 times. The detection solution remained stable with only a 0.6% decrease in absorbance compared to the original after storing it in a refrigerated environment at 3 °C for 14 days. The method proposed in this study for detecting glucose using FC blue light Mini-LEDs MOI reduces the use of peroxidase. In addition, it has a wide detection range that includes blood as well as non-invasive saliva and tear fluids, providing patients with a miniaturized, highly sensitive, and quantifiable glucose detection system.

Mesoporous silica-supported platinum nanocatalysts for colorimetric detection of glucose, cholesterol, and C-reactive protein

Noble metal nanoparticles decorated on a catalyst support with a large specific surface area can exhibit enhanced catalytic activity. To this end, a synthetic method to heterogeneously and evenly nucleate...

A phenylboronic acid-based smart photonic crystal hydrogel sensor for colorimetric detection of glucose

A phenylboronic acid-based smart photonic crystal hydrogel (PNAPB) sensor with good recyclability was reported for the sensitive and colorimetric detection of glucose.

Encapsulation of an enzyme-immobilized smart polymer membrane in a metal-organic framework for enhancement of catalytic performance.

Encapsulation of enzymes within porous materials has shown great promise for protecting enzymes from denaturation, increasing their tolerance to harsh environments and promoting their industrialization. However, controlling the conformational freedom of the encapsulated enzymes to enhance their catalytic performance remains a great challenge. To address this issue, herein, following immobilization of GOx and HRP on a thermo-responsive porous poly(styrene-maleic-anhydride-N-isopropylacrylamide) (PSMN) membrane, a GOx-HRP@PSMN@HZIF-8 composite was fabricated by encapsulating GOx-HRP@PSMN in hollow ZIF-8 (HZIF-8) with liposome (L) as the sacrificial template. The improved conformational freedom for enzymes arising from the hollow cavity formed in ZIF-8 through the removal of L enhanced the mass transfer and dramatically promoted the catalytic activity of the composite. Interestingly, at high temperature, the coiled PN moiety in PSMN provided the confinement effect for GOx-HRP, which also significantly boosted the catalytic performance of the composites. Compared to the maximum catalytic reaction rates (Vmax) of GOx-HRP@PSMN@LZIF-8, the free enzyme and GOx-HRP@ZIF-8, the Vmax of the GOx-HRP@PSMN@HZIF-8 composite exhibited an impressive 17.8-fold, 10.8-fold and 6.0-fold enhancement at 37 °C, respectively. The proposed composites successfully demonstrated their potential as catalytic platforms for the colorimetric detection of glucose in a cascade reaction. This study paves a new way for overcoming the current limitations of immobilizing enzymes in porous materials and the use of smart polymers for the potential fabrication of enzyme@polymer@MOF composites with tunable conformational freedom and confinement effect.

Mesoporous silica-supported platinum nanocatalysts for colorimetric detection of glucose, cholesterol, and C-reactive protein.

Noble metal nanoparticles decorated on a catalyst support with a large specific surface area can exhibit enhanced catalytic activity. To this end, a synthetic method to heterogeneously and evenly nucleate platinum nanoparticles (Pt NPs) onto mesoporous silica nanoparticles (MSNs) is developed. The obtained Pt NP-modified MSNs (Pt-MSNs) are characterized as a thin layer of 3 nm-sized Pt NPs densely assembled on the MSN surface, by which the throughput of the peroxidase-like activity of Pt-MSNs is greatly improved. The utility of Pt-MSNs in colorimetric detection of analytes is validated for two different assay schemes. Firstly, colloidally dispersed Pt-MSNs are employed as a peroxidase-mimic in a two-step cascade reaction to quantitate glucose/cholesterol based on the amount of H2O2 produced by glucose/cholesterol oxidase. Secondly, detection of C-reactive protein (CRP) is conducted on a solid substrate by adopting a sandwich immunoassay format. Detection limits are estimated to be 20 μM, 55 μM, and 3.9 pM for glucose, cholesterol, and CRP, respectively.

Colorimetric detection of glucose with smartphone-coupled µPADs: harnessing machine learning algorithms in variable lighting environments

Recent advances in microfluidic paper-based analytical devices (µPADs) have shown immense potential for point-of-care testing (POCT) in resource-constrained settings, especially for monitoring glucose levels in patients with diabetes. However, the practical adoption of smartphone-coupled µPADs has been limited due to the variability in ambient lighting conditions, which affects the colorimetric detection. In this study, we have developed a machine learning-based algorithm together with a flash/no-flash technic, adaptable to various µPADs and capable of accurately monitoring plasma glucose levels across a wide range (25 µM to 30 mM), addressing issues related to environmental illumination variations, and shooting angles.The algorithm is implemented in an Android application, Gluco estimator. It utilizes images captured by smartphones and incorporates intelligent feature engineering. The XYZ color space is adopted for device-independent analysis. KI and TMB color indicators are used to enhance resolution for low and high glucose concentrations, respectively. The EBC classifier, combined with a handcrafted feature set, exhibits outstanding performance, achieving an accuracy of 95% and 91% for TMB and KI, respectively. Additionally, multiple linear regression (MLR) yields high reliability among regression models, with R2 values of 0.95 at 0.25 µM to 3 mM and 0.97 at 3–30 mM. This work represents a significant stride toward realizing a portable, high-resolution, and reliable smartphone-coupled µPAD in uncontrolled environments.

Colorimetric and fluorescent detection of glucose based on Fe7S8 nanosheets catalyzed oxidation of o-phenylenediamine

Fe7S8 nanosheets (Fe7S8 NSs) was prepared from ferrous sulfate and thiourea, showing peroxidase-like activity and enabling the oxidation of o-phenylenediamine (OPD) in the presence of H2O2 to produce 2,3-diaminophenol (DAP) with strong absorption and fluorescence peaks at 450 and 560 nm, respectively. Furthermore, both the level of absorbance at 450 nm (A450) and the intensity of fluorescence at 560 nm (F560) depended on the concentration of H2O2. As a result, a dual response (colorimetry and fluorescence) method for the assay of H2O2 was established. Due to the fact that H2O2 can be produced from glucose oxidase catalyzed glucose oxidation, A450 and F560 were further used for indirectdetermination of glucose. The results indicated that the absorbance and fluorescence responses were closely related to glucose concentration in the range of 1.0–100 μM and 1.0––70 μM with the detection limit of 0.83 and 0.52 μM, respectively. To verify its practicality, the method has been used for determining glucose in human serum samples with recoveries ranging from 92.2 to 106.2 %, suggesting its promising potential applications.

A smartphone-assisted one-step bicolor colorimetric detection of glucose in neutral environment based on molecularly imprinted polymer nanozymes

In order to improve the specificity and the peroxidase-like activity of nanozyme at the neutral pH as well as to facilitate the naked-eye visual detection of the analyte concentration, a nanozyme based on molecularly imprinted polymers (MIPNs) for selective and bicolor colorimetric detection of glucose in neutral environment was developed. Compared with free nanozyme, the synthesized MIPNs showed a better catalytic capability, with a catalytic efficiency (kcat/Km) 9.5 times higher than that of free nanozyme. The kinetics experiment showed that the MIPNs demonstrated a fast kinetic feature and the kinetic data fitted a pseudo-first-order model. In practical application, the color of the detection system changed gradually from pink to blue as the glucose concentration increased in a broad linear range from 0 to 3 mM, with a detection limit of 6.22 μM. The colorimetric visualization of glucose concentration was read with a smartphone and no other instrument was needed. Therefore, a manageable and highly efficient method for the MIPNs-catalyzed visualization at the neutral pH and the one-step bicolor visual detection was constructed. This newly established method may also provide a new idea for further development and application of nanozymes.