Glucose Oxidase Molecules Research Articles

Conductive single enzyme nanocomposites prepared by in-situ growth of nanoscale polyaniline for high performance enzymatic bioelectrode.

Enzyme-based electrochemical biosensors hold great promise for applications in health/disease monitoring, drug discovery, and environmental monitoring. However, inherently non-conductive nature of proteinaceous enzymes often hampers effective electron transfer at enzyme-electrode interface, limiting biosensor performance of enzyme bioelectrodes. To address this problem, we present an approach to synthesize polyaniline (PAN)-based conductive single enzyme nanocomposites of glucose oxidase (GOx) (denoted as PAN-GOx). To prevent multimerization of enzymes during nanocomposite synthesis and enable single enzyme wrapping, we activate GOx surface with phenylamine groups based on the programmed diffusion of reactants in the reaction solution. Subsequent in-situ polymerization enables the synthesis of nanoscale conductive PAN layer (∼2.7nm thickness) grafted from individual GOx molecule. PAN-GOx retains 83% and 74% of its specific activity and catalytic efficiency, respectively, compared to free GOx, while demonstrating a ∼500% improved conductivity. Furthermore, PAN-GOx-based glucose biosensors show an approximately 16- and 3-fold higher sensitivity compared to biosensors prepared by using free GOx and a mixture of PAN and GOx, respectively. This study provides a facile method to fabricate conductive single enzyme nanocomposites with enhanced electron transfer, which can potentially be further modified and/or compounded with conductive materials for demonstrating high performance enzymatic bioelectrodes.

Cascade Hydroxyl Radical-Generating and Ferroptosis-Inducing Nanofiber System for the Therapy of Oral Squamous Cell Carcinoma.

Nanofiber (NF) membrane systems that can provide cascade catalytic reaction and ferroptosis induction were developed for oral cancer therapy. Glucose oxidase (GOx) and aminoferrocene (AF) were introduced into the NF system for glucose deprivation/H2O2 generation and OH radical generation, respectively. GOx offers starvation therapy and AF (including iron) provides chemodynamic therapy/ferroptosis for combating oral cancer. GOx (water-soluble) and AF (poorly water-soluble) molecules were successfully entrapped in the NF membrane via an electrospinning process. GOx and AF were incorporated into the polyvinyl alcohol (PVA)-based NF, resulting in PVA/GOx/AF NF with fast disintegration and immediate drug-release properties. In oral squamous cell carcinoma (YD-9 cells), the PVA/GOx/AF NF group exhibited higher cytotoxicity, antiproliferation potential, cellular ROS level, apoptosis induction, lipid ROS level, and malondialdehyde level compared to the other NF groups. The electrospun PVA/GOx/AF NF can be directly applied to oral cancer without causing pain, offering starvation/chemodynamic therapy and ferroptosis induction.

Сенсорное покрытие на основе липидного ленгмюровского монослоя с молекулами фермента глюкозооксидазы

A sensor coating was created based on a Langmuir monolayer of 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) with immobilized molecules of the enzyme glucose oxidase and its sensor properties were studied. The process of incorporation of glucose oxidase enzyme molecules into a Langmuir monolayer of phospholipid DPPE molecules was studied using the compression isotherm method. Adsorption of glucose oxidase molecules has an expanding effect on the Langmuir monolayer of DPPE and leads to an increase in the area per molecule from 32.5 Å2 to 49 Å2 and a decrease in the compression modulus of the monolayer from 133 mN/m to 83 mN/m. Also, the adsorption of glucose oxidase leads to an increase in the desorption coefficient of the monolayer into the kd subphase from 0.5·10-3 to 1.2·10-3. The morphology of films with immobilized enzyme molecules at different adsorption times was characterized by atomic force microscopy. Increasing the enzyme adsorption time leads to a decrease in the surface roughness of the formed film from 3.6 nm at 5 minutes to 2.4 nm at 60 minutes. The formed DPPE monolayers with immobilized enzyme molecules were transferred to graphite electrodes. Their sensory properties were studied using cyclic voltammetry and impedance measurements. The resulting coatings were sensitive to glucose in solutions with concentrations from 0 to 1 mg/ml. The presence of a linear concentration dependence of the maximum and minimum currents and resistances in the specified concentration range makes the created films promising for use as touch coatings.

Structure-Function Studies of Glucose Oxidase in the Presence of Carbon Nanotubes and Bio-Graphene for the Development of Electrochemical Glucose Biosensors.

In this work, we investigated the effect of multi-walled carbon nanotubes (MWCNTs) and bio-graphene (bG) on the structure and activity of glucose oxidase (GOx), as well as on the performance of the respective electrochemical glucose biosensors. Various spectroscopic techniques were applied to evaluate conformational changes in GOx molecules induced by the presence of MWCNTs and bG. The results showed that MWCNTs induced changes in the flavin adenine dinucleotide (FAD) prosthetic group of GOx, and the tryptophan residues were exposed to a more hydrophobic environment. Moreover, MWCNTs caused protein unfolding and conversion of α-helix to β-sheet structure, whereas bG did not affect the secondary and tertiary structure of GOx. The effect of the structural changes was mirrored by a decrease in the activity of GOx (7%) in the presence of MWCNTs, whereas the enzyme preserved its activity in the presence of bG. The beneficial properties of bG over MWCNTs on GOx activity were further supported by electrochemical data at two glucose biosensors based on GOx entrapped in chitosan gel in the presence of bG or MWCNTs. bG-based biosensors exhibited a 1.33-fold increased sensitivity and improved reproducibility for determining glucose over the sweat-relevant concentration range of glucose.

Unraveling the Molecular Dynamics of Glucose Oxidase Desorption Induced by Argon Cluster Collision.

The bombardment of a protein multilayer target by an energetic argon cluster ion beam enables protein transfer onto a collector in the vacuum while preserving their bioactivity (iBEAM method). In parallel to this new soft-landing variant, protein transfer in the gas phase is a prerequisite for their characterization by mass spectrometry. The successful transfer of bioactive lysozymes (14 kDa) by cluster-induced soft landing and its mechanistic explanation by molecular dynamics (MD) simulations have sparked an important inquiry: Can heavier biomolecules be desorbed while maintaining their tridimensional structure and hence their bioactivity? To address this question, we employed MD simulations using a reactive force field (ReaxFF). Specifically, the Ar cluster-induced desorption of glucose oxidase from either a gold substrate or a lysozyme underlayer was modeled using the LAMMPS code. First, the force field parameters were trained by computing the dissociation energetics of a series of organic molecules with ReaxFF and DFT, in order to realistically describe N-S and O-S interactions in the bombarded glucose oxidase molecule. Second, bombardment simulations investigated the effects of cluster size (ranging from 1000 to 10000 Ar atoms) and kinetic energy (1.5 and 3.0 eV/atom) on the structural features and energetics of the desorbing glucose oxidase. Our results show that large argon clusters (≥7000) are needed to desorb glucose oxidase from a gold surface, yet protein fragmentation and/or pronounced denaturation occur. However, the transfer of structurally preserved glucose oxidase in the gas phase is predicted by the simulations when an organic layer is used as a substrate.

Glucose Oxidase/Egg White Protein Microparticles with a Redox Mediator for Glucose Biosensors on a Screen-Printed Electrode and a Decomposable Electrode.

Glucose oxidase (GOx) is a typical model enzyme used to create biosensors. Exploring a strategy to prepare ready-to-use functional enzymatic microparticles combining GOx and food-based proteins offers compelling advantages. However, no reports exist on the integration of egg white materials to synthesize functional biorecognition particles with glucose oxidation catalytic functions for electrochemical biosensors. Here, we demonstrate functional microparticles combining egg white proteins, GOx, and 9,10-phenanthrenequinone (PQ). The egg white proteins crosslink to form three-dimensional scaffolds to accommodate GOx and redox molecules. The PQ mediator enhances electron transfer between the electrode surface and the GOx enzyme's flavin adenine dinucleotides. The functional microparticles are directly applied to the printed electrode. The performance of these microparticles is evaluated using a screen-printed carbon nanotube (CNT)-modified electrode coated with GOx/PQ/egg white protein microparticles. The analytical performance of the system exhibits a linear range of 0.125-40 mM, with a maximum current (Imax) and a Michaelis-Menten constant (Km) being 0.2 µA and 4.6 mM, respectively. Additionally, a decomposable electrode composed of CNTs and edible oil conjugated with functional enzyme microparticles is shown to undergo degradation under gastric conditions. Utilizing food-based proteins to accommodate enzymes and to create redox-active microparticles for catalyzing glucose oxidation offers advantages in developing affordable and degradable bioelectrodes. This concept holds promise for advancing biocompatible electrodes in biosensor and bioelectronics applications.

Fluorescence-Amplified Origami Microneedle Device for Quantitatively Monitoring Blood Glucose.

Exploration of clinically acceptable blood glucose monitors has been engaging in the past decades, yet the ability to quantitatively detect blood glucose in a painless, accurate, and highly sensitive manner remains limited. Herein, a fluorescence-amplified origami microneedle (FAOM) device is described that integrates tubular DNA-origami nanostructures and glucose oxidase molecules into its inner network to quantitatively monitor blood glucose. The skin-attached FAOM device can collect glucose molecules in situ and transfer the input into a proton signal after the oxidase's catalysis. The proton-driven mechanical reconfiguration of DNA-origami tubes separates fluorescent molecules and their quenchers, eventually amplifying the glucose-correlated fluorescence signal. The function equation established on clinical examinees suggests that FAOM can report blood glucose in a highly sensitive and quantitative manner. In clinical blind tests, the FAOM achieves well-matched accuracy (98.70±4.77%) compared with a commercial blood biochemical analyzer, fully meeting the requirements of accurate blood glucose monitoring. The FAOM device can be inserted into skin tissue in a trivially painful manner and with minimal leakage of DNA origami, substantially improving the tolerance and compliance of the blood glucose test.

Characterization of Enzymatic Glucose Biosensors Based on A Glassy Carbon Electrode Modified with MoS2 Nanorods

: In this work, molybdenum disulfide (MoS2) nanorods (NRs) were prepared by a simple hydrothermal method. A sensitive electrochemical glucose biosensor was developed based on the immobilization of glucose oxidase (GOx) on MoS2 NRs modified glassy carbon electrode (GCE). The SnO2 NRs were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). SnO2 NRs have large specific area and can load large amounts of GOx molecules. The cyclic voltammetry (CV) of GOx/MoS2 NR/GCE exhibited a linear relationship between the peak current density of CV with glucose concentration in the range of 3.0 mM to 7.0 mM with the limit of detection (LOD) of 3.0 mM and high sensitivity of mA.mM. The parameters affecting the oxidation current density such as pH, temperature, GOx concentration were also investigated. This study demonstrates the feasibility of realizing inexpensive, reliable, and highly effective performance glucose biosensors using MoS2 nanorods.
 

In silico study of interaction of (ZnO)12 nanocluster to glucose oxidase-FAD in absence and presence of glucose

Diabetes mellitus is one of the foremost global concerns, as it has impacted millions of lives. Therefore, there is an urgent need to develop a technology for continuous glucose monitoring in vivo. In the current study, we employed computational methods such as docking, MD simulations, and MM/GBSA, to obtain molecular insights into the interaction between (ZnO)12 nanocluster and glucose oxidase (GOx) that cannot be obtained through experiments alone. For this, theoretical modeling of the 3D cage-like (ZnO)12 nanocluster in ground state configuration was performed. Further docking of (ZnO)12 nanocluster with GOx molecule was carried out to find the nano-bio-interaction of (ZnO)12-GOx complex. To understand the whole interaction and dynamics of (ZnO)12-GOx-FAD-with and without glucose, we performed MD simulation and MM/GBSA analysis of (ZnO)12-GOx-FAD complex and glucose-(ZnO)12-GOx-FAD complex separately. The interaction was found to be stable, and the binding energy of (ZnO)12 to GOx-FAD increases in the presence of glucose by 6 kcal mol−1. This may be helpful in nano probing of the interaction of GOx with glucose. It can help in making a device like fluorescence resonance energy transfer (FRET) based nano-biosensor to monitor the glucose level in pre and post diabetic patient. Communicated by Ramaswamy H. Sarma

Materials and Carriers Development for Glucose-Responsive Insulin

ConspectusInsulin replacement therapy is an essential and effective treatment strategy for controlling the blood glucose level (BGL) of people without sufficient endogenous insulin production. However, insulin therapy faces challenges such as daily multiple injections and hypoglycemia risk arising from its narrow therapeutic index, which together leads to poor BGL control. Thus, glucose-responsive insulin delivery systems that can mimic β-cell function are developed to improve BGL control and reduce injection frequency. Glucose-responsive materials-based insulin delivery systems are competent in tightly controlling the BGL with an additional benefit of reducing the hypoglycemia risk. Glucose-responsive materials generally work together with three major glucose-sensing elements: glucose oxidase (GOx), phenylboronic acid (PBA), and glucose-binding molecules. Based on glucose-sensing elements, glucose-responsive materials are rationally designed to sense the change in glucose concentration or indirect signals associated with glucose fluctuation, such as pH, H2O2 concentration, and O2 level, and adjust their physical or chemical characteristics accordingly. Many advanced glucose-responsive materials have been developed along this line, aiming to achieve robust glucose-responsive insulin release performance and elevate their therapeutic outcome. These advanced materials mainly include organic materials such as biomacromolecules, synthetic polymers, polypeptides, liposomes, and inorganic materials such as calcium phosphate (Ca3(PO4)2) and metal organic frameworks (MOFs). Built on these glucose-responsive materials, other groups and we have developed various carriers such as hydrogels, micro/nanoparticles, liposomes, complexes, cell–drug conjugates, and microneedle (MN) array patches. These delivery systems can release insulin via glucose-stimulated swelling/contraction, dissolution, pore size change, charge reversal, and polymer deterioration. Also, these carriers are continuously under development to accelerate responsive rate, increase response index, and improve biocompatibility. Our group focuses on the synthesis of glucose-responsive materials and the design of glucose-responsive MN array patches, hydrogels, insulin complexes, and cell–drug conjugates for the treatment of diabetes in a dose-, spatial-, and temporal-controlled fashion. These closed-loop insulin delivery systems can respond to BGL alternation and secrete the correct amount of insulin accordingly. Also, MN array patches have the additional merits of reducing pain and easy administration.In this Account, we briefly introduce the glucose-responsive mechanisms and the relevant requirements of materials that can work cooperatively with these mechanisms. Then, we highlight our group’s work in preparing various materials for constructing glucose-responsive carriers. We are mainly aiming to improve glucose-responsive properties, administration feasibility, and in vivo biocompatibility. The challenges and perspectives associated with glucose-responsive materials for clinical translation are also discussed. We envision that our glucose-responsive MN array patch for insulin release will facilitate the clinical use of glucose-responsive materials.

Polydopamine mediator for glucose oxidation reaction and its use for membraneless enzymatic biofuel cells

Polydopamine (PDA) is used as a biocompatible mediator for fabricating glucose oxidase (GOx) based bioanode of enzymatic biofuel cells (EBFCs). Through the autoxidation and polymerization of dopamine monomer, spherical PDA particles are well synthesized, and their chemical and optical characteristics are verified. Although the durability of bioanode including CNT and PDA (CNT/PDA/GOx/Nafion) is poor, when catalyst including polyethyleneimine (PEI) upper layer (CNT/PDA/GOx/PEI/Nafion) is fabricated, CNT/PDA/GOx/PEI/Nafion shows excellent durability. This indicates PEI plays a critical role in suppressing the leaching out of PDA and GOx molecules. By the role of PEI, the anodic current density of CNT/PDA/GOx/PEI/Nafion (142.6 ± 1.98 μA cm−2 at 0.6 V (vs. Ag/AgCl)) is 17.3 times better than that of CNT/PDA/GOx/Nafion. When maximum power density (MPD) of EBFC using CNT/PDA/GOx/PEI/Nafion is measured, that of EBFC including membrane and platinum-based air–cathode is 552.8 ± 5.4 µW cm−2, and that of membraneless EBFC including bilirubin oxidase biocathode is 135.2 ± 5.45 μW cm−2, which is better than that of other reported EBFCs studies. This confirms that the suggested new catalyst is a viable option as bioanode for EBFC.

Electrochemically confined effects on single enzyme detection with nanopipettes

• Label-free detection of single enzymes using nanopipettes with varying orifices in near physiological solutions. • The ionic enhancement sensing strategy for single protein. • Nanopore confinement effect modulated translocation behavior of single enzymes. Dynamic conformational changes of enzymes during enzyme catalysis are crucial to the catalytic activities, however the subtle variations are usually buried in ensemble-averaged measurements. The nanopore sensing technique is a promising tool for single-molecule analysis by providing a nanoscale confined space to capture and insolate a single analyte from a bulk solution. Here, we employed nanopipettes with different diameters to analyze the translocation process of single glucose oxidase molecules in an electrolyte solution with low salt concentration. The unique confinement effect of pore including the volume exclusion and charge effect contributed to the current fluctuations, resulting in the current blockade and current enhancement protein traversing through the nanopipettes tip orifice with diameters of 67 nm and 34 nm, respectively. Our research shed light that the interaction between the enzyme and inner wall of nanopipette could significantly extend the duration time of analyte at the orifice, which may facilitate to capturing a single molecule and tracing the subtle conformational changes during enzyme catalysis without any labeling, providing new insights into single enzyme analysis.

Immobilization of Glucose Oxidase on pH-Responsive Polyimide-Polyacrylic Acid Smart Membranes Fabricated Using 248 nm KrF Excimer Laser for Drug Delivery

The permeability of polyimide–polyacrylic acid (PI-PAAc) pH-responsive membrane fabricated using a 248 nm KrF laser was investigated. These membranes were further immobilized with glucose oxidase enzyme, which led to the successful development of a glucose-responsive membrane. The base PI membranes were developed using a simple photolithographic technique. Further grafting of PAAc inside the pores was carried out using the same laser wavelength. The effect of various solution parameters and laser parameters were studied and discussed in detail in our previous work. A variety of grafting yields were obtained by changing laser exposure time. Glucose Oxidase (GOD) enzyme was then immobilized on the membrane using a carbodiimide-based amidation method. The polyacrylic acid grafted inside the pores shows pH-responsive gating. The immobilized GOD molecules show glucose sensitivity and convert the glucose into gluconic acid. The experiment results show that these membranes can detect the amount of glucose and release the corresponding solute amount.

A comparative study of greener alternatives for nanocellulose production from sugarcane bagasse

Use of enzyme for extraction of nanocellulose from sugarcane bagasse is greener alternative. Literature indicates that effectiveness of these enzymes can be improved by auxiliary enzymes or mediators. In the current study, extraction of nanocellulose using laccase with these moderators, auxiliary enzyme glucose oxidase and mediator molecule, ABTS [2,2′-azinobis(3-ethylbenzthiazoline-6-sulfonate)] individually was done. Cellulose and lignin content, FT-IR, TGA and DSC analysis, XRD, SEM and PSA were done. Enzyme moderators improved the performance of laccase in lignin degradation. Lignin and cellulose content, crystallinity were used as parameters to optimize the concentrations, which was found to be ABTS (at 1.4 mM) and glucose oxidase (at 0.15 mg ml−1). At the optimal concentration, nanocellulose was extracted. Properties of nanocellulose obtained from both routes were compared. Size analysis revealed 339 nm and 636 nm for nanocellulose obtained with glucose oxidase and ABTS, respectively. Defibrillation was better in the case of the former one as seen from SEM.Graphical

Development of a new biocathode for a single enzyme biofuel cell fuelled by glucose

In this study, we reported the development of Prussian blue (PB), poly(pyrrole-2-carboxylic acid) (PPCA), and glucose oxidase (GOx) biocomposite modified graphite rod (GR) electrode as a potential biocathode for single enzyme biofuel cell fuelled by glucose. In order to design the biocathode, the GR electrode was coated with a composite of PB particles embedded in the PPCA shell and an additional layer of PPCA by cyclic voltammetry. Meanwhile, GOx molecules were covalently attached to the carboxyl groups of PPCA by an amide bond. The optimal conditions for the biocathode preparation were elaborated experimentally. After optimization, the developed biocathode showed excellent electrocatalytic activity toward the reduction of H2O2 formed during GOx catalyzed glucose oxidation at a low potential of 0.1 V vs Ag/AgCl, as well as good electrochemical performance. An electrocatalytic current density of 31.68 ± 2.70 μA/cm2 and open-circuit potential (OCP) of 293.34 ± 15.70 mV in O2-saturated 10 mM glucose solution at pH 6.0 were recorded. A maximal OCP of 430.15 ± 15.10 mV was recorded at 98.86 mM of glucose. In addition, the biocathode showed good operational stability, maintaining 95.53 ± 0.15% of the initial response after 14 days. These results suggest that this simply designed biocathode can be applied to the construction of a glucose-powered single enzyme biofuel cell.

Maximizing the enzyme immobilization of enzymatic glucose biofuel cells through hierarchically structured reduced graphene oxide

The number of immobilized glucose oxidase (GOx) molecules is considerably increased by the structural modification of reduced graphene oxide (rGO), and the performance of enzymatic biofuel cells (EBFCs) is positively affected by the modification process. To do this, new rGO with three-dimensional open porous structure is formed by spray freeze drying method (sprGO), while tetrathiafulvalene (TTF) as mediator, and GOx are sequentially immobilized onto sprGO. To improve the loading amount of catalyst, rGO structure is modified to open porous sprGO structure possessing numerous anchoring sites, after which gelatin film crosslinked by glutaraldehyde is fabricated onto sprGO to prevent any losses of other components (sprGO/[TTF-GOx]/crosslinked-gelatin). Specific surface area and charge transfer resistance of sprGO are quantitatively measured, and the actual amount of immobilized GOx and the performance of EBFC using this catalyst are electrochemically examined. With this, it is found that the amount of GOx immobilized in sprGO/[TTF-GOx]/crosslinked-gelatin is twice better that in rGO/[TTF-GOx]/crosslinked-gelatin. More specifically, EBFC using this catalyst shows open circuit voltage of 0.85 V and maximum power density of 380 μW/cm2, and this is 1.4 times better than that using rGO/[TTF-GOx]/crosslinked-gelatin. These results indicate that the amount of immobilized GOx strongly affects the performance capabilities of EBFCs.

Biodegradable cascade nanocatalysts enable tumor-microenvironment remodeling for controllable CO release and targeted/synergistic cancer nanotherapy

Gas therapy as an emerging therapeutic modality for cancer treatment is still facing critical challenges such as precise delivery and controllable release of therapeutic gas. Herein, we report a “tumor-microenvironment remodeling” strategy for in situ sustained release of CO gas and magnetic resonance imaging (MRI)-monitored targeted/synergistic cancer gas/starvation nanotherapy by engineering cascade biodegradable nanocatalyst. The nanocatalyst integrates the enzyme catalyst glucose oxidase (GOD) and H2O2-sensitive molecule manganese carbonyl (MnCO) entrapped biodegradable hollow mesoporous organosilica nanoparticles (HMONs). Especially, GOD is initially exploited as a gatekeeper, followed by surface engineering with arginine-glycine-aspartic acid (RGD) for specifically targeting αvβ3 integrin-overexpressed cancer cells. The GOD is dissociated under reduced pH to release the loaded MnCO, and sequentially produce gluconic acid and H2O2 to remodel the TME for facilitating the in situ generation of CO/Mn2+. As systematically demonstrated both at cellular level and in an animal tumor xenograft model, the engineered nanocatalyst achieves superior theranostics performance via combinatorial CO gas and starving-like nanotherapy. This work provides an effective strategy for augmenting CO-mediated antitumor efficacy by remodeling the tumor microenvironment.

Cyclic reactions-mediated self-supply of H2O2 and O2 for cooperative chemodynamic/starvation cancer therapy

Hydroxyl radical (·OH)-mediated chemodynamic therapy (CDT) and glucose oxidase (GOx)-based starvation therapy (ST) are two emerging antitumor strategies, limited by acid/H2O2 deficiency and tumor hypoxia, respectively. Herein, we developed a liposomal nanoplatform co-delivering Fe(OH)3-doped CaO2 nanocomposites and GOx molecules for synergistic CDT/ST with a complementary effect. Based on Fenton reactions initiated by iron ions, CaO2-supplied H2O2 could not only generate ·OH for H2O2-sufficient CDT, but also produce O2 to promote the catalytic efficiency of GOx under hypoxia. In return, the enhanced ST generated gluconic acid and H2O2, further amplifying CDT. Through in vitro and in vivo experiments, we demonstrated that such a mutually reinforced modality based on the cyclic Fenton/starvation reactions provided a novel and potent anticancer mechanism for the effective treatment of hypoxic cancers.

A New One-Pot Way to Prepare Enzyme-Containing Coordination Polymers by Sonochemistry.

Enzyme-containing Coordination Polymers (CPs) were prepared by a one-pot sonochemical method, mixing Glucose Oxidase (GOx) enzyme, 4,4'-bipyridine as spacer ligand, and chloride zinc salt. The reaction took place in a very short time (a few minutes) with a minimum use of solvents compared to conventional methods. The obtained composite material, named GOx-[Zn(4,4'-bipy)Cl₂]∞, resulted from embedding the GOx molecules into uniformly sized [Zn(4,4'-bipy)Cl₂] nanocrystals. The structural and thermal characterization, confirmed that the adopted strategy allows the preparation of hybrid bio-nanomaterials in a very fast, facile and eco-friendly method, by simply synthesising the [Zn(4,4'-bipy)Cl₂] nanocrystals in the presence of the enzyme.

Bird nest-like zinc oxide nanostructures for sensitive electrochemical glucose biosensor

In this research, a novel bird nest-like zinc oxide (BN-ZnO) nanostructures were prepared by a simple solvothermal method. A sensitive electrochemical glucose biosensor was for the first time developed based on the immobilization of glucose oxidase (GOx) on nanostructured BN-ZnO modified electrode. The BN-ZnO nanostructure and the resultant biosensor were characterized by scanning electron microscope, X-ray diffraction spectroscopy, Fourier transform infrared spectroscopy, and electrochemical impedance spectroscopy. BN-ZnO nanostructures have large specific surface area and can load large amounts of GOx molecules. Meanwhile, BN-ZnO provides an excellent microenvironment to retain the native bioactivity of enzymes and to promote direct electron transfer between GOx and electrode surface. The proposed biosensor shows a wide linear range of 0.005–1.6 mmol/L, high sensitivity of 15.6 mA L mol−1 cm−2 with a low detection limit of 0.004 mmol/L. The resulting biosensor also shows excellent selectivity, acceptable stability and reproducibility, and can be successfully applied in the detection of glucose in human serum samples at −0.37 V.