共查询到20条相似文献,搜索用时 120 毫秒
1.
本文以中性红为核,二氧化硅为壳,利用反相微乳液技术,通过正硅酸四乙酯的水解制备了掺杂有中性红的二氧化硅纳米粒子,并用TEM技术进行了表征。核中性红能够催化测定葡萄糖,乳酸和L-谷氨酸的反应,而壳二氧化硅不仅克服了电活性物质中性红易流失的缺点,且具有高的生物亲和性。分别与葡萄糖氧化酶、乳酸氧化酶以及L-谷氨酸氧化酶混合后,修饰在碳阵列电极表面。最后在该酶阵列电极表面滴加一层Nafion, 防止电活性物质抗坏血酸、尿酸等的干扰。该酶阵列传感器与流动注射分析技术(FIA)相结合,可应用于同时检测大鼠血样中的葡萄糖,乳酸和L-谷氨酸浓度。该方法无需通过传统的色谱柱的分离,大大简化了实验条件,为这一领域的研究提供了有效的分析方法。 相似文献
2.
Zakir Hossain SM Shinohara H Wang F Kitano H 《Analytical and bioanalytical chemistry》2007,389(6):1961-1966
There is an increasing interest in new strategies to detect neurotransmitters released from nerve cells in real time for brain
science, drug assessment, and so on. Previously we reported real-time monitoring of dopamine release from nerve model cells
by enzyme-catalyzed luminescence measurement with tyramine oxidase and peroxidase. In the present study, the system was modified
with glutamate oxidase instead of tyramine oxidase to detect L-glutamate sensitively (≈ 10 nM) and rapidly with high temporal resolution (<1 s). We applied this modified method successfully
to perform real-time monitoring of L-glutamate release from brain model cell (C6 glioma cell) using a luminescence plate reader upon stimulation with high concentration
of KCl (>10 mM) or 5-hydroxytryptamine (>1 μM). The measurement solution was not toxic and therefore the L-glutamate release from the cell was measured by the second stimulation after exchanging the measurement solution. We conclude
that the developed monitoring system is suitable for real-time detection of dynamic L-glutamate release from nerve cells in vitro and will be suitable for application in assessment of drugs acting on the nervous
system.
Figure Enzyme luminescence detection of L-glutamate released from cells 相似文献
3.
Nakamura N Negishi K Hirano A Sugawara M 《Analytical and bioanalytical chemistry》2005,383(4):660-667
Real-time monitoring of L-glutamate release from various neuronal regions of mouse hippocampal slices under ischemia (a glucose-free hypoxia condition)
is described. A glass capillary microelectrode with a tip size of ∼10 μm containing a very small volume (∼2 μL) of a solution
of glutamate oxidase (GluOx) and ascorbate oxidase was used. First, the amperometric response behavior of the electrode at
0 V versus Ag/AgCl was characterized with a standard glutamate solution in terms of continuous measurements, effect of oxygen,
viscosity of solution and concentration dependence. The electrode was applied to the real-time monitoring of L-glutamate released from different neuronal regions of acute hippocampal slices submerged in a hypoxia solution. The time-resolved
amounts of L-glutamate released at various neuronal regions (CA1, CA3 and DG) of mouse hippocampal slices were quantified and compared
with the reported L-glutamate fluxes using difference-image analysis during ischemia. 相似文献
4.
A glass capillary-based enzyme electrode (tip size ≈10 μm) was implanted in the target neuronal region, i.e., dentate gyrus
(DG) or cornu ammonis 1 (CA1), of acute brain slices at a depth of ≈10 μm from the slice surface in order to allow the monitoring
of chemical stimulant-induced changes in L-glutamate levels. First, the sampling behavior of a glass capillary in a slice was investigated by visualizing the transport
of a fluorescence dye. Then, the electrode was applied to real-time monitoring of L-glutamate release in acute hippocampal slices stimulated by surface application of a stimulant solution. The extracellular
application of KCl (0.10 M) increased the glutamate levels in the DG and CA1 regions, respectively. The enhancement of L-glutamate concentration at DG was much larger than at CA1. The application of tetraethylammonium chloride (TEA) (25 mM) enhanced
the L-glutamate level in the DG region and the enhanced level did not return to the initial value before TEA application even when
washed with an artificial cerebrospinal fluid (ACSF). The usefulness of a surface-implanted capillary electrode for monitoring
L-glutamate release in acute brain slices is discussed. 相似文献
5.
Jun Yao Hong Xu Ningning Shi Xin Cao Xiaohai Feng Sha Li Pingkai Ouyang 《Applied biochemistry and biotechnology》2010,160(8):2332-2341
Bacillus subtilis NX-2 produces γ-polyglutamic acid (γ-PGA) when using glucose and l-glutamate as carbon sources. The conversion of carbon sources into γ-PGA was analyzed with the 13C-NMR method after enriching the media with 13C-labeled glucose. The results showed that the percentage of γ-PGA monomers derived from glucose was relatively low, approximately
6% and 9%, respectively, with an initial glucose concentration of 30 and 40 g L−1. It was concluded that glucose was utilized mainly as the growth-limiting substrate for cell growth and supplied the required
energy during γ-PGA biosynthesis, while l-glutamate was preferred as the main substrate for γ-PGA formation. To achieve an efficient conversion of l-glutamate and enhance the γ-PGA production, a fed-batch culture was proposed by feeding of glucose. By this method, supplied
l-glutamate (40 g L−1) was completely depleted, and γ-PGA yield was attained 42 g L−1. 相似文献
6.
Silver nanoparticles enhanced glucose oxidase electrodes were prepared on the basis of chitosan matrix. The enzyme electrodes exhibited high sensitivity and excellent response performance to glucose with a linear range from 1×10?6 to 8×10?3 mol · L?1. And the time reaching the steady‐state amperometric response was less than 5 seconds. The inhibition percentage of this enzyme electrode against copper ions concentration was linear ranging from 1.2×10?6 to 5×10?5 mol · L?1. These properties of enzyme electrodes are probably due to the excellent electron transfer of silver nanoparticles and the orientation of glucose oxidase molecule. 相似文献
7.
An electrochemical in vivo flow-injection system with an on-line microdialysis sampling is proposed for the simultaneous monitoring of L-lactate and glucose in rat brain. In the first stage of the operation, the dialysate from the microdialysis probe is delivered to a sample loop of the six-way autoinjector by perfusing Ringer's solution for 80 s at 5 microl min(-1). In the second stage, the dialysate collected in the sample loop is automatically injected for 10 s into the flow-injection line. Injected dialysate is split into two streams and two portions pass through two channels with two different immobilized enzyme reactors (glucose oxidase and lactate oxidase immobilized reactors) to produce hydrogen peroxide from glucose and L-lactate in the dialysate. After a subsequent confluence of the streams, produced hydrogen peroxide can be detected amperometrically at a downstream poly(1,2-diaminobenzene) film-coated platinum electrode, without any interference from oxidizable species and proteins present in the dialysate. Because each channel has a different residence time, two peaks are obtained. The first peak corresponds to L-lactate and the second peak to glucose. The peak current is linearly related to the concentrations of L-lactate between 0.2 and 10 mM and glucose between 0.1 and 20 mM. The present method can be successfully applied to the simultaneous in vivo monitoring of L-lactate and glucose in rat brain. The analytical speed is 45 dialysates h(-1). 相似文献
8.
Paolo Bollella Sanjiv Sharma Anthony Edward George Cass Riccarda Antiochia 《Electroanalysis》2019,31(2):374-382
Here we report the first mediated pain free microneedle‐based biosensor array for the continuous and simultaneous monitoring of lactate and glucose in artificial interstitial fluid (ISF). The gold surface of the microneedles has been modified by electrodeposition of Au‐multiwalled carbon nanotubes (MWCNTs) and successively by electropolymerization of the redox mediator, methylene blue (MB). Functionalization of the Au‐MWCNTs/polyMB platform with the lactate oxidase (LOX) enzyme (working electrode 1) and with the FAD‐Glucose dehydrogenase (FADGDH) enzyme (working electrode 2) enabled the continuous monitoring of lactate and glucose in the artificial ISF. The lactate biosensor exhibited a high sensitivity (797.4±38.1 μA cm?2 mM?1), a good linear range (10–100 μM) with a detection limit of 3 μM. The performance of the glucose biosensor were also good with a sensitivity of 405.2±24.1 μA cm?2 mM?1, a linear range between 0.05 and 5 mM and a detection limit of 7 μM. The biosensor array was tested to detect the amount of lactate generated after 100 minutes of cycling exercise (12 mM) and of glucose after a normal meal for a healthy patient (10 mM). The results reveal that the new microneedles‐based biosensor array seems to be a promising tool for the development of real‐time wearable devices with a variety of sport medicine and clinical care applications. 相似文献
9.
Immobilization of bioactive molecules on the surface of magnetic nanoparticles is of great interest, because the magnetic properties of these bioconjugates promise to greatly improve the delivery and recovery of biomolecules in biomedical applications. Here we present the preparation and functionalization of magnetite (Fe3O4) nanoparticles 20 nm in diameter and the successful covalent conjugation of the enzyme glucose oxidase to the amino-modified nanoparticle surface. Functionalization of the magnetic nanoparticle surface with amino groups greatly increased the amount and activity of the immobilized enzyme compared with immobilization procedures involving physical adsorption. The enzymatic activity of the glucose oxidase-coated magnetic nanoparticles was investigated by monitoring oxygen consumption during the enzymatic oxidation of glucose using a ruthenium phenanthroline fluorescent complex for oxygen sensing. The glucose oxidase-coated magnetite nanoparticles could function as nanometric glucose sensors in glucose solutions of concentrations up to 20 mmol L–1. Immobilization of glucose oxidase on the nanoparticles also increased the stability of the enzyme. When stored at 4°C the nanoparticle suspensions maintained their bioactivity for up to 3 months. 相似文献
10.
Bruno P. Crulhas Juliane R. Sempionatto Murilo F. Cabral Sergiy Minko Valber A. Pedrosa 《Electroanalysis》2014,26(4):815-822
The construction and characterization of a biosensor based on polymer brushes is reported. The use of polymer brushes combined with nanoparticles was applied to show its suitability as a biosensor platform – with glucose oxidase as an enzyme probe. The biosensor demonstrated a pH‐sensitive on‐off property, and it was further used to control or modulate the electrochemical responses. In terms of the kinetic behavior, we were able to show the changing in the kinetic parameters of glucose oxidase operating in “on” and “off” state of the polymer brushes. The performance of the bioelectrode was investigated by chronoamperometry, impedance electrochemistry and cyclic voltammetric techniques. At optimized experimental conditions the dynamic concentration range was 2.0 to 16.0 mmol L?1 with a detection limit of 5.6×10–6 mol L?1. The repeatability of current responses for injections of 5.0 mmol L?1 glucose was evaluated to be 5.3 % (n=10). The resulting biosensor seemed to provide the enzymes with a biocompatible nanoenvironment as it sustained the enhanced enzyme activity for an extended time and promoted possible good electron transfer through the polymer brushes to the electrode. 相似文献
11.
D. V. Vokhmyanina E. E. Karyakina E. A. Andreev A. A. Karyakin 《Moscow University Chemistry Bulletin》2018,73(5):216-222
A planar multibiosensor for the simultaneous determination of glucose and lactate is developed by combining the Prussian Blue-based electrocatalyst and the protocol for immobilization of glucose oxidase and lactate oxidase enzymes from solutions with a high content of an organic solvent. High sensitivity coefficients (>80 mA M–1 cm–2 for lactate and >20 mA M –1 cm–2 for glucose) are demonstrated by the multibiosensors operating in the flow-injection mode in a thin-layer measuring cell. The linear range of the analyzed concentration is 1–500 μM for lactate and 5–1000 μM for glucose. A multibiosensor can be used repeatedly (the exhibited operational stability is not less than 100 measurements without the need for recalibration), which allows using it for the analysis of diluted blood samples and blood serum. The electrocatalytic system with a multibiosensor demonstrates performance characteristics that are superior to the commercial analyzers. 相似文献
12.
Yodthong Baimark Mangkorn Srisa-ard Jirasak Threeprom Nual-Anong Narkkong 《Colloid and polymer science》2007,285(13):1521-1525
Nanoparticle colloids of methoxy poly(ethylene glycol)-b-poly(D,L-lactide) (MPEG-b-PDLL) diblock copolymer were prepared by a modified spontaneous emulsification solvent diffusion method using acetone/ethanol
as the mixture organic solvents. The MPEG-b-PDLL was synthesized by ring-opening polymerization of D,L-lactide using stannous octoate and MPEG with molecular weight of 5,000 g/mol as the initiating system. The MPEG-b-PDLL obtained was an amorphous polymer with molecular weight of 73,600 g/mol. Influences of acetone/ethanol (v/v) ratios
and Tween 80 surfactant concentrations on characteristics of the colloidal nanoparticles were investigated and discussed.
Light-scattering analysis showed that average diameters of the surfactant-free colloidal nanoparticles were in the range of
86–124 nm. The nanoparticle sizes decreased as the ethanol ratio increased. The Tween 80 did not show the significant effect
on the nanoparticle sizes. Scanning electron micrographs of dried nanoparticles that demonstrated the aggregation of most
particles suggested they were the soft nanoparticles. However, the dried nanoparticle morphology can be observed from scanning
electron microscopy as having a spherical shape and smooth surfaces. 相似文献
13.
Endo H Hayashi Y Kitani Y Ren H Hayashi T Nagashima Y 《Analytical and bioanalytical chemistry》2008,391(4):1255-1261
l-Lysine (l-Lys) in living bodies is critical for metabolism; therefore, determination of its levels in food is important. Most enzymatic
methods for l-Lys analysis are performed using l-lysine oxidase (LyOx), but commercially manufactured LyOx is generally not highly selective for l-Lys among amino acids. We previously isolated LyOx as an antibacterial protein secreted from the skin of the rockfish Sebastes schlegeli. In the present study, we developed an optical enzyme sensor system for rapid and continuous determination of l-Lys using this LyOx. The system comprised an immobilized LyOx membrane, an optical oxygen probe, a flow system, and a personal
computer. The amount of l-Lys was detected as a decrease in the oxygen concentration due to the LyOx reaction. The specificity of the sensor was examined
against various amino acids. The sensor response was specific for l-Lys. Good reproducibility was obtained in 58 assays. The response of the sensor using commercially prepared LyOx was unstable
compared with the response using LyOx isolated in our laboratory. Our sensor system could be used for 5 weeks without our
having to change the enzyme membrane. The calibration curve for a standard l-Lys solution was linear from 0.1 to 3.0 mmol L−1. One assay could be completed within 2 min. The sensor was applied to determine the l-Lys content in food samples such as bonito cooking water and scallop hepatopancreas. The values obtained using the sensor
and conventional high-performance liquid chromatography methods were well correlated. 相似文献
14.
《Electroanalysis》2006,18(15):1499-1504
An amperometric method for the determination of glucose using a screen printed carbon electrode is reported. The electrode material was bulk modified with rhodium dioxide and the enzyme glucose oxidase immobilized in a Nafion‐film on the electrode surface and investigated for its ability to serve as a detector of glucose in flow injection analysis. The sensor exhibited a linear increase of the amperometric signal with the concentration of glucose in the range of 1–250 mg L?1 with a detection limit (evaluated as 3σ) of 0.2 mg L?1 under optimized flow rate of 0.4 mL min?1 in 0.1 M phosphate buffer (pH 7.5) carrier. At the potential applied (?0.2 V vs. Ag/AgCl), interferences from redox species present in the sample matrix were negligible. The biosensor reported here retained its activity for more than 40 injections or 4 months of storage at 6 °C. The RSD was determined as 1.8% for a glucose concentration of 25 mg L?1 (n=5) with a typical response time of about 28 s. 相似文献
15.
A sensitive enzymed‐based biosensor for glucose has been obtained by introducing dendrimer encapsulated Pt nanoparticles via a layer‐by‐layer assembling method. The free amine groups located on each poly(amidoamine) dendrimer molecule were exploited to covalently attach enzyme to the dendrimer chains using carbodiimide coupling. The resultant enzyme electrodes are shown to have excellent sensitivity (as high as 30.33 μA mM?1 cm?2) and a limit of detection (about 0.1 μmol L?1), depending on metal nanoparticles within dendrimers and the biocompatibility of dendrimers, the linear response range to glucose (from 5 μM to 1.0 mM), a fast response time (within 5 s), and good reproducibility (<8% relative standard deviation between electrodes at low substrate concentration). The sensitivities, and stabilities determined experimentally have demonstrated the potential of dendrimer encapsulated Pt nanoparticles as a novel candidate for enzymatic glucose biosensors. 相似文献
16.
Glucose 2-oxidase (pyranose oxidase, pyranose:oxygen-2-oxidoreductase, EC 1.1.3.10) from Coriolus versicolor catalyses the oxidation of d-glucose at carbon 2 in the presence of molecular O2 producing d-glucosone (2-keto-glucose and d-arabino-2-hexosulose) and H2O2. It was used to convert d-glucose into d-glucosone at moderate pressures (i.e. up to 150 bar) with compressed air in a modified commercial batch reactor. Several
parameters affecting biocatalysis at moderate pressures were investigated as follows: pressure, [enzyme], [glucose], pH, temperature,
nature of fluid and the presence of catalase. Glucose 2-oxidase was purified by immobilized metal affinity chromatography
on epoxy-activated Sepharose 6B-IDA-Cu(II) column at pH 6.0. The rate of bioconversion of d-glucose increased with the pressure since an increase in the pressure with compressed air resulted in higher rates of conversion.
On the other hand, the presence of catalase increased the rate of reaction which strongly suggests that H2O2 acted as inhibitor for this reaction. The rate of bioconversion of d-glucose by glucose 2-oxidase in the presence of either nitrogen or supercritical CO2 at 110 bar was very low compared with the use of compressed air at the same pressure. The optimum temperature (55°C) and
pH (5.0) of d-glucose bioconversion as well as kinetic parameters for this enzyme were determined under moderate pressure. The activation
energy (E
a) was 32.08 kJ mol−1 and kinetic parameters (V
max, K
m, K
cat and K
cat/K
m) for this bioconversion were 8.8 U mg−1 protein, 2.95 mM, 30.81 s−1 and 10,444.06 s−1 M−1, respectively. The biomass of C. versicolor as well as the cell-free extract containing glucose 2-oxidase activity were also useful for bioconversion of d-glucose at moderate pressures. The enzyme was apparently stable at moderate pressures since such pressures did not affect
significantly the enzyme activity. 相似文献
17.
An enzymatic method for determining L-malic acid in wine based on an L-malate sensing layer with nicotinamide adenine dinucleotide (NAD+), L-malate dehydrogenase (L-MDH) and diaphorase (DI), immobilized by sol-gel technology, was constructed and evaluated. The sol-gel glass was prepared
with tetramethoxysilane (TMOS), water and HCl. L-MDH catalyzes the reaction between L-malate and NAD+, producing NADH, whose fluorescence (λ
exc = 340 nm, λ
em = 430 nm) could be directly related to the amount of L-malate. NADH is converted to NAD+ by applying hexacyanoferrate(III) as oxidant in the presence of DI. Some parameters affecting sol-gel encapsulation and the
pH of the enzymatic reaction were studied. The sensing layer has a dynamic range of 0.1–1.0 g/L of L-malate and a long-term storage stability of 25 days. It exhibits acceptable reproducibility [s
r(%)≈10] and allows six regenerations. The content of L-malic acid was determined for different types of wine, and polyvinylpolypyrrolidone (PVPP) was used as a bleaching agent
with red wine. The results obtained for the wine samples using the sensing layer are comparable to those obtained from a reference
method based on UV-vis molecular absorption spectrometry, if the matrix effect is corrected for. 相似文献
18.
Electroactive nanostructured membranes have been produced by the layer-by-layer (LbL) technique, and used to make electrochemical enzyme biosensors for glucose by modification with cobalt hexacyanoferrate redox mediator and immobilisation of glucose oxidase enzyme. Indium tin oxide (ITO) glass electrodes were modified with up to three bilayers of polyamidoamine (PAMAM) dendrimers containing gold nanoparticles and poly(vinylsulfonate) (PVS). The gold nanoparticles were covered with cobalt hexacyanoferrate that functioned as a redox mediator, allowing the modified electrode to be used to detect H2O2, the product of the oxidase enzymatic reaction, at 0.0 V vs. SCE. Enzyme was then immobilised by cross-linking with glutaraldehyde. Several parameters for optimisation of the glucose biosensor were investigated, including the number of deposited bilayers, the enzyme immobilisation protocol and the concentrations of immobilised enzyme and of the protein that was crosslinked with PAMAM. The latter was used to provide glucose oxidase with a friendly environment, in order to preserve its bioactivity. The optimised biosensor, with three bilayers, has high sensitivity and operational stability, with a detection limit of 6.1 μM and an apparent Michaelis–Menten constant of 0.20 mM. It showed good selectivity against interferents and is suitable for glucose measurements in natural samples. 相似文献
19.
Cong Qin Chao ChenQingji Xie Lihua WangXiuhui He Yi HuangYaping Zhou Fangyun XieDawei Yang Shouzhuo Yao 《Analytica chimica acta》2012
Sodium alginate (AlgNa) and poly(diallyldimethylammonium chloride) (PDDA) were mixed to obtain an interpenetrating polymer composite via electrostatic interaction and then cast on an Au electrode surface, followed by incorporation of metal ions (e.g. Fe3+ or Ca2+, to form AlgFe or AlgCa hydrogel) and glucose oxidase (GOx) (or lactate oxidase (LOx)), to prepare amperometric enzyme electrodes. The interactions of PDDA, Alg, and Fe3+ are studied by visual inspection as well as microscopic and electrochemical methods. Under optimized conditions, the PDDA-AlgFe-enzyme/Au and PDDA-AlgCa-enzyme/Au electrodes can give good analytical performance (e.g. nM-scale limit of detection of glucose or lactate, and sensitivities > 50 μA cm−2 mM−1) in the first-generation biosensing mode, which are better than the reported analogs using typical polysaccharide biopolymers as enzyme-immobilization matrices. The enzyme electrodes also worked well in the second-generation biosensing mode in the coexistence of p-benzoquione or ferrocene monocarboxylic acid artificial mediator. Biofuel cells (BFCs) with the enzyme electrodes as the bioanodes and glucose (or lactate) as the biofuel were also fabricated with satisfactory results. The proposed protocols for preparation of high performance Alg-based biocomposites may find wide applications in bioanalysis. 相似文献
20.
Yinyin Wei Ningdan Zhang Ying Li Prof. Dr. Guoyue Shi Prof. Dr. Litong Jin 《中国化学》2010,28(12):2489-2493
A highly efficient enzyme immobilization method has been developed for electrochemical biosensors using polydopamine films with gold nanoparticles (AuNPs) embedded. This simple enzyme fabrication method can be performed in very mild conditions and stored in a long time with high bioactivity. The fabricated amperometric glucose biosensor exhibited a high and reproducible sensitivity, wide linear dynamic range and low limit of detection (LOD) (0.1 μmol·L?1). A low value of 1.5 mmol·L?1 for the apparent Michaelis‐Menten constant KappM was obtained. The high sensitivity, wide linear range, good reproducibility and stability make this biosensor a promising candidate for portable amperometric glucose biosensor. 相似文献