Oxygen Concentration In Solution Research Articles

Effect of terahertz radiation on the transport properties of albumin: binding with metal ions

The effect of terahertz radiation on clusterization of bovine serum albumin (BSA) molecules and on BSA binding with nickel, cobalt and cadmium ions is investigated by means of high performance liquid chromatography and EPR spectroscopy under variation of the concentration of molecular oxygen in solution. Irradiation is detected to remove steric hindrance for oxygen adsorption. The degree of nickel and cobalt ion binding with irradiated BSA samples is substantially higher than with non-irradiated ones, while for cadmium the binding degree is the same and rather low in both cases. The functional groups in BSA molecule participating in metal ion binding are revealed by means of modeling.

The effects of sodium sulfite on Helicobacter pylori by establishing a hypoxic environment

Helicobacter pylori (H. pylori) is an obligate microaerobion and does not survive in low oxygen. Sodium sulfite (SS) reacts and consume oxygen in solutions. The present study aimed to investigate the effects of SS on H. pylori. The effects of SS on oxygen concentrations in solutions and on H. pylori in vivo and in vitro were examined, and the mechanisms involved were explored. The results showed that SS decreased the oxygen concentration in water and artificial gastric juice. In Columbia blood agar and special peptone broth, SS concentration-dependently inhibited the proliferation of H. pylori ATCC43504 and Sydney strain-1 in Columbia blood agar or special peptone broth, and dose-dependently decreased the number of H. pylori in Mongolian gerbils and Kunming mouse infection models. The H. pylori was relapsed in 2 weeks withdrawal and the recurrence in the SS group was lower than that in the positive triple drug group. These effects were superior to positive triple drugs. After SS treatments, the cell membrane and cytoplasm structure of H. pylori were disrupted. SS-induced oxygen-free environment initially blocked aerobic respiration, triggered oxidative stress, disturbed energy production. In conclusion, SS consumes oxygen and creates an oxygen-free environment in which H. pylori does not survive. The present study provides a new strategy and perspective for the clinical treatment of H. pylori infectious disease.

Efficient degassing and ppm-level oxygen monitoring flow chemistry system.

Low oxygen levels are critical for a long range of chemical transformations carried out in both flow and batch chemistry. Here, we present an inline continuous flow degassing system based on a gas-permeable membrane inside a vacuum chamber for achieving and monitoring ppm-level oxygen concentrations in solutions. The oxygen presence was monitored with a molecular oxygen probe and a continuously running UV-vis spectrometer. An automated setup for discovering optimal reaction conditions for minimal oxygen presence was devised. The parameters tested were: flow rate, vacuum pressure, solvent back-pressure, tube material, tube length and solvent oxygen solubility. The inline degassing system was proven to be effective in removing up to 99.9% of ambient oxygen from solvents at a flow rate of 300 μl min-1 and 4 mbar vacuum pressure inside the degassing chamber. Reaching lower oxygen concentrations was limited by gas permeation in the tubing following the degassing unit, which could be addressed by purging large volume flow reactors with an inert gas after degassing or by using tubing with lower gas permeability, such as stainless steel tubing. Among all factors, oxygen solubility in solvents was found to play a significant role in achieving efficient degassing of solvents. The data presented here can be used to choose optimal experimental parameters for oxygen-sensitive reactions in flow chemistry reaction setups. The data were also fitted to an analytically derived model from simple differential equations in physical context of the experiment.

Mechanistic kinetic modelling of enzyme-catalysed oxidation reactions of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA)

Six enzymes were tested against HMF and its oxidation intermediates to determine substrate specificity, product yield and pathways. A Michaelis–Menten kinetic mathematical model was constructed and some rate parameters calculated. The best 2,5-diformylfuran (DFF) productivity was obtained with alcohol oxidase (AO) and 10.0 mM HMF, where 3.0 mM DFF was formed, followed by galactose oxidase (GO) and 10.0 mM HMF with a 0.5 mM DFF yield. Oxygen concentration in solution remained unchanged during processes. Substrate concentration affected only AO, where around 10 mol.% more DFF was formed with 5.0 mM HMF. The model was mostly in good agreement with single-enzyme reactions. Multi-enzyme reactions were used for model validation. The combination of AO and catalase was optimal, converting 10.0 mM HMF to 9.7 mM DFF. Small discrepancy between measured and modeled multi-enzyme reactions was observed due to the exclusion of the specific interactions in mechanisms.

Multiplexed Bioanalysis Based on Light-Sensitive Electrodes

IntroductionQuantum dots (QDs) have become attractive tools in bioanalysis because of their advantageous optical and electrochemical properties. This relates to applications exploiting fluorescence, electrochemiluminescence or photocurrent generation [1]. For the latter case QDs are immobilized on conductive electrodes. By light excitation charge carriers are formed inside the nanoparticles which can be used for photocurrent generation. Signal chains can be constructed when appropriate donor or acceptor components are present in solution. The special feature of such electrodes is that the response is triggered by illumination of the sensing electrode [1]. In this study, a light-addressable photoelectrochemical sensor was built by coupling QDs with oxidases to detect different enzyme substrates.Results and ConclusionsFirst CdSe/ZnS QDs have been immobilised via a dithiol compound on gold electrodes. Two different enzymes, glucose oxidase (GOD) and sarcosine oxidase (SOD) have been deposited on this QDs-electrode at spatially well resolved places. Here small spots have been achieved by a dropping method. A laser beam is moved over the spots to detect photocurrents. Since oxygen can act as electron acceptor at the illuminated QDs the photocurrent is correlated to the oxygen concentration in solution. By action of the enzymes in the presence of the corresponding substrate a competitive situation for oxygen is created in front of the QD layer and thus, the photocurrent decreases [2, 3]. Since this happens in a concentration dependent way, analysis of the enzyme substrate is feasible.Furthermore, due to the spatially separated immobilisation of the two enzymes, an independent read-out of the two enzyme reactions is possible. The results indicate good lateral resolution and selectivity of the multi-detection system without any crosstalk between the two sensing regions and also without any response at regions, which have not been modified with an enzyme [4].After that, the possibility of an imaging of the enzyme spot by photocurrent measurement has been studied. When the laser is moved over the spot of GOD with a constant speed, the size of the spot can be determined from the photocurrent - time curve (with a defined moving speed). The photocurrent correlates to different local enzyme activities. Consequently, an imaging of the enzyme activity distribution on the surface has also been achieved by this method.

Quantification of dissolved O2 in bulk aqueous solutions and porous media using NMR relaxometry

Effects of dissolved paramagnetic oxygen (O2) in water on 1H nuclear magnetic resonance (NMR) Carr-Purcell-Meiboom-Gill (CPMG) experiments is evaluated at a 1H Larmor frequency of 2 MHz. Dissolution of O2 into water significantly reduces the 1H transverse relaxation coefficient (T2). For deoxygenated water, T2 is 3388 ms, water at ambient atmospheric conditions (7.4 mg/L O2) exhibits a T2 of 2465 ms, and dissolution of 2710 mg/L O2 further reduces T2 to 36 ms. The results were fit with an empirical model to facilitate prediction of T2 times for bulk water as a function of paramagnetic oxygen concentrations in solution. Dissolved O2 also greatly influences 1H NMR CPMG experiments of confined water in a model system composed of Berea sandstone. For this system, 90 mg/L O2 in H2O enhances T2 relaxation of bulk water such that the relaxation time is comparable to physically confined water in the sandstone pores. Given the sensitivity of NMR T2 coefficients to paramagnetic oxygen, low-field NMR-based characterization of fluid and porous media structure requires control of dissolved oxygen, as geospatial variation in the partial pressure of O2 alone is expected to perturb fluid and pore relaxation times by up to 60 and 36%, respectively.

Multiplexed Bioanalysis Based on Light-sensitive Electrodes

Introduction Quantum dots (QDs) have become attractive tools in bioanalysis because of their advantageous optical and electrochemical properties. This relates to applications exploiting fluorescence, electrochemiluminescence or photocurrent generation [1]. For the latter case QDs are immobilized on conductive electrodes. By light excitation charge carriers are formed inside the nanoparticles which can be used for photocurrent generation. Signal chains can be constructed when appropriate donor or acceptor components are present in solution. The special feature of such electrodes is that the response is triggered by illumination of the sensing electrode [1]. In this study, a light-addressable photoelectrochemical sensor was built by coupling QDs with oxidases to detect different enzyme substrates. Results and Conclusions At first CdSe/ZnS QDs have been immobilised via a dithiol compound on gold electrodes. Two different enzymes, glucose oxidase (GOD) and sarcosine oxidase (SOD) have been deposited on this QDs-electrode at spatially well resolved places. Here small spots have been achieved by a dropping method. A laser beam is moved over the spots to detect photocurrents. Since oxygen can act as electron acceptor at the illuminated QDs the photocurrent is correlated to the oxygen concentration in solution. By action of the enzymes in the presence of the corresponding substrate a competitive situation for oxygen is created in front of the QD layer and thus, the photocurrent decreases [2, 3]. Since this happens in a concentration dependent way, analysis of the enzyme substrate is feasible.Furthermore, due to the spatially separated immobilisation of the two enzymes, an independent read-out of the two enzyme reactions is possible. The results indicate good lateral resolution and selectivity of the multi-detection system without any crosstalk between the two sensing regions and also without any response at regions, which have not been modified with an enzyme [4].After that, the possibility of an imaging of the enzyme spot by photocurrent measurement has been studied. When the laser is moved over the spot of GOD with a constant speed, the size of the spot can be determined from the photocurrent - time curve (with a defined moving speed). The photocurrent correlates to different local enzyme activities. Consequently, an imaging of the enzyme activity distribution on the surface has also been achieved by this method.

Laccase-Catalyzed Reduction of Oxygen at Electrodes Modified by Carbon Nanotubes with Adsorbed Promazine or Acetosyringone

One of the problems with the use of enzymes as catalysts in biofuel cells is to achieve good contact between the enzyme and the electrode surface. One solution to this problem is the use of various nanostructures such as carbon nanotubes, fullerenes, graphene derivatives, gold nanoparticles, as well as mediators for the construction of electrodes. Acetosyringone and promazine adsorbed on glassy carbon electrodes (GCEs) covered with multiwall carbon nanotubes (MWCNTs) and laccase were used as biocathodes. These mediators showed very efficient adsorption on modified glassy carbon electrodes covered with MWCNTs and enabled efficient and stable adsorption of laccase, which acts as the bioelectrocatalyst. Very good electrical contact between the electrode surface and the laccase enzymatic active sites made it possible to increase the catalytic current density of oxygen-reduction by about 82% compared to electrodes without mediators. Application of acetosyringone and promazine used in the construction of biocathode also improved the current and power of the biobattery ca. twice comparing to the system without mediators. The device output reached the power that equaled approximately 2 mW/cm2 at 0.8 V and open circuit potential (OCP) was 1.6 V. The systems elaborated proved also useful in oxygen sensing and allowed to determine lower oxygen concentrations in solution compared to the GCE modified with MWCNTs and laccase alone. The electrode showed also better stability in long-timescale measurements.

Theoretical study of the dissolution kinetics of galena and cerussite in an abandoned mining area (Zaida mine, Morocco)

In the abandoned mine in Zaida, the pit lakes filled with water constitute significant water reserves. In these lakes, the waters are permanently in contact with ore deposit (cerussite and galena). The modelling of the interaction of waters with this mineralization shows that cerussite dissolves more rapidly than galena. This dissolution is controlled by the pH and dissolved oxygen concentration in solution. The lead concentrations recorded in these lakes come largely from the dissolution of cerussite.

Tunable electron affinity with electronic band alignment of solution processed dielectric

We report the tunability of the electronic band structure, especially the electron affinity, of an all-inorganic precursor processed sol-gel aluminium oxide phosphate dielectric by the influence of processing temperature. The dielectric offers tunable electron affinity ranging from 1.42 eV to 0.72 eV with the change in processing temperature from as-prepared to 1000 °C, respectively. The remarkable change in electron affinity is ascribed to the variation in the bulk oxygen concentration in solution processed oxide. As a result, the leakage current of the dielectric is affected significantly by a factor of ∼103.

Photodriven Oxygen Removal via Chromophore-Mediated Singlet Oxygen Sensitization and Chemical Capture.

We report a general, photochemical method for the rapid deoxygenation of organic solvents and aqueous solutions via visible light excitation of transition metal chromophores (TMCs) in the presence of singlet oxygen scavenging substrates. Either 2,5-dimethylfuran or an amino acid (histidine or tryptophan methyl ester) was used as the substrate in conjunction with an iridium or ruthenium TMC in toluene, acetonitrile, or water. This behavior is described for solutions with chromophore concentrations that are pertinent for both luminescence and transient absorption spectroscopies. These results consistently produce TMC lifetimes comparable to those measured using traditional inert gas sparging and freeze-pump-thaw techniques. This method has the added benefits of providing long-term stability (days to months); economical preparation due to use of inexpensive, commercially available oxygen scrubbing substrates; and negligible size and weight footprints compared to traditional methods. Furthermore, attainment of dissolved [O2] < 50 μM makes this method relevant to any solution application requiring low dissolved oxygen concentration in solution, provided that the oxygenated substrate does not interfere with the intended chemical process.

Negligible interaction of [Ru(Phen)3]2+ with human serum albumin makes it promising for a reliable invivo assessment of the tissue oxygenation

The interaction between a ruthenium - based water soluble oxygen probe ([Ru(Phen)3]2+, phen - phenanthroline) and human serum albumin (HSA) was investigated with the aim of describing the influence of HSA on the [Ru(Phen)3]2+ luminescence properties. Nowadays, several oxygen sensitive luminescent probes are used to determine the oxygen level in different compartments of living organisms. However, they can interact, depending on their hydrophilic/hydrophobic characters, with various serum proteins, and/or lipids, during their utilization for invivo oxygen measurement. Since HSA is the most abundant serum protein in most biological organisms, its presence may affect the spectral properties of the employed probes and, consequently, the determination of the oxygen concentration. Having this in mind, we have applied several spectroscopic and calorimetric techniques to study [Ru(Phen)3]2+ - HSA mixtures. Only a negligible effect of HSA on the absorption and luminescence spectra of [Ru(Phen)3]2+ was observed. In addition, differential scanning calorimetric studies showed that [Ru(Phen)3]2+ does not significantly influence HSA thermal stability. Importantly, [Ru(Phen)3]2+ retained a reliable luminescence lifetime sensitivity to the oxygen concentration in solutions supplemented with HSA and in U87 MG cancer cells. Finally, the biodistribution of [Ru(Phen)3]2+ in the presence of serum proteins in the blood stream of chick embryo's chorioallantoic membrane (CAM) was investigated. Fast [Ru(Phen)3]2+ and similar extravasations were observed in the presence or absence of CAM-serum. We can conclude that HSA-[Ru(Phen)3]2+ complex interaction does not significantly influence the potential of [Ru(Phen)3]2+ to be a suitable candidate for a reliable oxygen probe in living organisms.

Sensing oxygen at the millisecond time-scale using an ultra-microelectrode array (UMEA)

We report a novel sensing protocol based on ultra-short (<5ms) measurements, which is using a dedicated sensor consisting of an ultra-microelectrode array (UMEA) for monitoring the concentration in dissolved oxygen concentrations in solution. The UMEA sensor is fabricated from Pt and oxide-nitride-oxide (ONO) as an insulating material, and electrodes are recessed in a glass substrate. The UMEA sensor is operated in its linear regime, and the oxygen concentration in solution is derived in less than 5ms from the slope of the measured current I as a function of 1/√t, t being the measurement time. To validate the proposed measurement protocol and to calibrate the sensor, variations in the concentration of dissolved oxygen are monitored simultaneously using the UMEA-based sensor and an external electrochemical sensor in a 10-mL wet-cell. An excellent agreement (R2=0.994) is found between the two sensors, and a sensitivity of 0.49nAs−0.5/mg/L is determined for the UMEA sensor operated in this ultra-short measurement regime. Finally, and most importantly, the amount of oxygen consumed during the electrochemical measurements in this configuration is drastically reduced, i.e., by about 10 orders of magnitude, compared to a commercial electrochemical sensor, which is very valuable to monitor in situ the respiratory activity of microtissues in nL volumes as found in microfluidic systems.

The influence of excitation radiation parameters on photosensitized generation of singlet oxygen in water

Photosensitized generation of singlet oxygen with the aid of Radahlorin® photosensitizer has been investigated. The dependences of the intensity of singlet oxygen phosphorescence and photosensitizer fluorescence on the excitation radiation wavelength in the range of 350–440 nm and on the irradiation dose have been obtained. The dependence of the ratio of the sensitizer fluorescence intensity at about 670 nm to the singlet oxygen phosphorescence intensity at a wavelength of 1270 nm on the excitation radiation wavelength is found to be nonmonotonic and have a minimum near the center of the absorption band on its red wing. The results obtained can be used to monitor the singlet oxygen concentration in solutions.

Transient study of the oxygen reduction reaction on reduced Pt and Pt alloys microelectrodes: evidence for the reduction of pre-adsorbed oxygen species linked to dissolved oxygen.

Using chronoamperometry at preconditioned oxide-free Pt microdisc electrodes in aqueous media, we investigated the oxygen reduction reaction (ORR) on the millisecond timescale and obtained results consistent with the reduction of oxygen species which adsorb on the electrode before the ORR is electrochemically driven. Furthermore these adsorbed species are clearly linked to oxygen in solution. At long times, the amperometric response is solely controlled by the diffusion of dissolved oxygen towards the microelectrode. However, at short times, typically below 50 ms, the reduction of pre-adsorbed oxygen produces a large extra current whose magnitude depends on the oxygen concentration in solution, deliberate electrode poisoning and the rest time before the potential step. Using sampled current voltammetry we show that this extra current affects the entire potential range of the ORR. Using microdisc electrodes made with Pt alloys we find that the amperometric response is sufficiently sensitive to distinguish oxygen coverage differences between Pt, Pt0.9Rh0.1 and Pt0.9Ir0.1 microdiscs. These unexpected and, to our knowledge, never previously reported results provide new insight into the oxygen reduction reaction on Pt. The existence over a wide potential range of irreversibly adsorbed oxygen species arising from dissolved oxygen and different from Pt oxide is particularly relevant to the development of oxygen reduction catalysts for low temperature fuel cells.

Effects of oxygen concentration in solution and uptake rate by roots on cut roses yield, and nutrients and sugars content in leaves

The response of rose flower yield to hypoxia has been discussed in the literature, but there is still a lack of sufficient data on plant performance as affected by dissolved oxygen concentration in solution (DOC) and uptake flux by roots, to support efficient aeration control. The objective was to study Rosa L. response to DOC by characterizing oxygen consumption rates, leaf contents of nutrients and sugars, and cut-flower yield. Five levels of DOC in solution, ranging from 7.5 to 1.7mg/L, were investigated. In winter and early spring DOC ≥2.5mg/L was sufficient to satisfy plant demands for oxygen. In late spring and summer the required DOC was ~5mg/L, corresponding to an O2 influx of 0.55mggfw−1h−1. When DOC in summer was 1.7mg/L the accumulation rate of Mn, Zn, P, Mg, and K in leaves was inhibited relative to DOC ~5mg/L, transpiration declined, starch and polymerized glucose accumulated in leaves, and cut-flower yield decreased. Indications in solution were reduced capacity to decrease pH after the May harvest, which stemmed from reduced H+ efflux from roots, and stronger decline in EC due to decreased transpiration.

Non-invasive determination of cellular oxygen consumption as novel cytotoxicity assay for nanomaterials

Investigating the safety of nanoparticles is essential for many fields of their applications, in particular for consumer products, food and medicines. The conventional dye and fluorescence-based cytotoxicity assays are limited by the interference of such readouts with nanomaterials. This holds in particular when nanomaterials have been fluorescently labelled for other purposes, for example, confocal microscopy. Moreover, most of these assays are invasive, that is, typically involve irreversible changes or destruction of cells and hence only allowing one endpoint measurement. Therefore, a non-invasive method for the detection of cytotoxicity was developed which is based on the automated online monitoring of the oxygen concentration in solution (SensorDish® Reader). Fluorescently labelled silica nanoparticles with different sizes and surface modifications were used as model systems to explore this novel assay. Thereby, the SensorDish® Reader allows a life documentation of the cellular behaviour and clarifies that size, time, concentration and surface modification of nanoparticles affect cellular viability.

Ratiometric Molecular Sensor for Monitoring Oxygen Levels in Living Cells

A ratiometric oxygen sensor (C343-Pro4-BTP) that uses coumarin 343 (blue in picture) as an oxygen-insensitive fluorophore and an iridium complex (BTP, red in picture) as an oxygen-sensitive phosphor can be used to determine the oxygen concentration in solution and in living cells, which was demonstrated by ratiometric measurements of the blue coumarin 343 fluorescence and the red BTP phosphorescence in C343-Pro4-BTP (see picture). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

The Comparison of Rotenone and an Environmentally Safe Insecticide (Azadirachtin) on Cultured Cell Respiration

Background: Both azadirachtin and rotenone, two botanical pesticides have shown inhibit the growth of cultured insect cells. The inhibitory effect of rotenone on cell growth is through disruption of electron transport chain, but exact mechanism of effect of azadirachtin on growth of cell is unknown. This study was carried out to compare the effect of these phytochemical on oxygen consumption by cultured cells . Methods: Electron transport and oxygen uptake were measured using the oxygen electrode, which continuously determines the concentration of oxygen in solution. Rotenone was used as a positive control to investigate if azadirachtin had its effect on respiration of the cells. Estimates of oxygen uptake for Sf9 and C6/36 were done at 30°C and for L929 at 37°C. Results: Preliminary results indicated that concentration of 10 4 M of azadirachtin had the maximum effect on cell respiration. Also rotenone in concentration of 10 -8 M reduced the cell respiration by 50%. However using purified mitochondria, the effect of azadirachtin on respiration rate was not significant . Conclusion: Interestingly in present test, both azadirachtin and rotenone could reduce the total oxygen consumption. Azadirachtin had only a minor effect on the respiration rate in both mammalian and insect cultured cells and there was only a slight difference between them. Due to low sensitivity of insect cells and also presence of same sensitivity in mammalian cells it seems that the effect of azadirachtin on cell respiration is different to that of rotenone. Also the results of this study suggest that while cell growth assessment .is not appropriate for all phytochemical pesticides, it is useful for those, such as azadirachtin and rotenone whose effect is on the essential mechanisms of insect cells in general .

Assessing bioenergetic function in response to oxidative stress by metabolic profiling

It is now clear that mitochondria are an important target for oxidative stress in a broad range of pathologies, including cardiovascular disease, diabetes, neurodegeneration, and cancer. Methods for assessing the impact of reactive species on isolated mitochondria are well established but constrained by the need for large amounts of material to prepare intact mitochondria for polarographic measurements. With the availability of high-resolution polarography and fluorescence techniques for the measurement of oxygen concentration in solution, measurements of mitochondrial function in intact cells can be made. Recently, the development of extracellular flux methods to monitor changes in oxygen concentration and pH in cultures of adherent cells in multiple-sample wells simultaneously has greatly enhanced the ability to measure bioenergetic function in response to oxidative stress. Here we describe these methods in detail using representative cell types from renal, cardiovascular, nervous, and tumorigenic model systems while illustrating the application of three protocols to analyze the bioenergetic response of cells to oxidative stress.