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Determination of mercury(II) ion by electrochemical cold vapor generation atomic absorption spectrometry.

A technique for determination of mercury is described; it is based on electrolytic reduction of Hg(II) ion on a graphite cathode, the trapping of mercury vapor and its volatilization into a quartz tube aligned in the optical path of an atomic absorption spectrometer. The electrochemical cell consisted of a graphite cathode and an anode operating with constant direct current for the production of mercury atoms. A pre-activated graphite rod was used as the cathode material. The optimum conditions for electrochemical generation of mercury cold vapor (the electrolysis time and current, the flow rate, the type of electrode and electrolyte) were investigated. The characteristic electrochemical data with chemical cold vapor using NaBH4-acid were compared. The presence of cadmium(II), arsenic(III), antimony(III), selenium(IV), bismuth(III), silver(I), lead(II), lithium(I), sodium(I) and potassium(I) showed interference effects which were eliminated by suitable separation techniques. The calibration curve is linear over the range of 5-90 ng ml(-1) mercury(II). The detection limit is 2 ng ml(-1) of Hg(II) and the RSD is 2.5% (n = 10) for 40 ng ml(-1). The accuracy and recovery of the method were investigated by analyzing spiked tap water and river water.

Journal Article↗

Failure to detect dexamethasone phosphate in the local venous blood postcathodic lontophoresis in humans.

STUDY DESIGN: A single-blind, 2-factor (4 treatments by 8 time points) repeated-measures study design. OBJECTIVE: To analytically determine dexamethasone and dexamethasone phosphate concentrations in plasma derived from proximal effluent venous blood, following cathodic iontophoresis. METHODS AND MEASURES: Six volunteers received the following dexamethasone phosphate (2.5 ml, 4 mg/ml) treatments to their wrists on separate occasions: cathodic iontophoresis (4 mA, 10 minutes or 4 mA, 20 minutes), passive application (10 or 20 minutes). Plasma samples from the ipsilateral antecubital vein were obtained 10 minutes prior to and half way through the treatment (5 or 10 minutes), at the end of the treatment (10 or 20 minutes), and posttreatment (15, 30, 60, 90, and 120 minutes). The present investigation examined: (1) the sensitivity and linearity of extraction and analysis of dexamethasone and dexamethasone phosphate; (2) the necessity for determining both; and (3) the plasma levels from proximal effluent venous blood following cathodic iontophoresis. RESULTS: The aggregate (n = 18) of the 6-point standard curves were linear for dexamethasone (r > 0.974) and dexamethasone phosphate (r > 0.829). In vitro dephosphorylation of dexamethasone phosphate to dexamethasone occurred in plasma at 37 degrees C and during freeze-thaw. Measurable dexamethasone or dexamethasone phosphate concentrations were absent at all time points and under all conditions in the human subjects. CONCLUSIONS: These results demonstrate the sensitivity of the current assay and the need for evaluating both forms of the drug, as in vitro dephosphorylation results in the presence of dexamethasone and dexamethasone phosphate in samples. Absence of measurable dexamethasone or dexamethasone phosphate in the proximal effluent venous blood may require re-evaluation of the extent of drug delivery during the clinical iontophoresis of dexamethasone phosphate.

Adult↗

Design of experimentation with a platinum-magnesium bioelectric battery.

The utilization of metal electrodes in the fabrication of a bioelectric battery has been the subject of intensive study for several years. Up to this date, subcutaneous cathodes of black platinum or of silver-silver chloride have been used in conjunction with anodes of aluminum or zinc. The subcutaneous black platinum is not reliable as a function of time due to the growth of overlying heterogeneous tissues. The utilization of a smooth platinum cathode in the right endoauricular position allows good reliability with time, but does not allow using a large surface area. Furthermore we have a reduction of the H-+ ions and not of the oxygen. A pure Domal magnesium anode was utilized with this cathode, which seemed to be a good compromise between to battery's voltage, its lifetime, and its lack of toxicity to body tissues.

Animals↗

Effects of water source, dilution, storage, and bacterial and fecal loads on the efficacy of electrolyzed oxidizing water for the control of Escherichia coli O157:H7.

To evaluate the potential of using electrolyzed oxidizing (EO) water for controlling Escherichia coli O157:H7 in water for livestock, the effects of water source, electrolyte concentration, dilution, storage conditions, and bacterial or fecal load on the oxidative reduction potential (ORP) and bactericidal activity of EO water were investigated. Anode and combined (7:3 anode:cathode, vol/vol) EO waters reduced the pH and increased the ORP of deionized water, whereas cathode EO water increased pH and lowered ORP. Minimum concentrations (vol/vol) of anode and combined EO waters required to kill 10(4) CFU/ml planktonic suspensions of E. coli O157:H7 strain H4420 were 0.5 and 2.0%, respectively. Cathode EO water did not inhibit H4420 at concentrations up to 16% (vol/vol). Higher concentrations of anode or combined EO water were required to elevate the ORP of irrigation or chlorinated tap water compared with that of deionized water. Addition of feces to EO water products (0.5% anode or 2.0% combined, vol/vol) significantly reduced (P < 0.001) their ORP values to < 700 mV in all water types. A relationship between ORP and bactericidal activity of EO water was observed. The dilute EO waters retained the capacity to eliminate a 10(4) CFU/ml inoculation of E. coli O157:H7 H4420 for at least 70 h regardless of exposure to UV light or storage temperature (4 versus 24 degrees C). At 95 h and beyond, UV exposure reduced ORP, significantly more so (P < 0.05) in open than in closed containers. Bactericidal activity of EO products (anode or combined) was lost in samples in which ORP value had fallen to < or = 848 mV. When stored in the dark, the diluted EO waters retained an ORP of > 848 mV and bactericidal efficacy for at least 125 h; with refrigeration (4 degrees C), these conditions were retained for at least 180 h. Results suggest that EO water may be an effective means by which to control E. coli O157:H7 in livestock water with low organic matter content.

Colony Count, Microbial↗

[Focal morphological changes in the bone tissue of the mandible and tibia of rabbits under the influence of different metal inclusions].

Morphological changes in bone tissue were studied in an experimental model with electrochemical polarization of the bone, which was achieved by applying electrodes (anode made of silver-palladium alloy SPS-250 and cathode of copper-aluminum alloy manufactured as orthodontic ligature wire) on the mandibular periosteum and tibial bone of rabbits. Macroscopic changes were as follows: osseous tissue hypertrophy at the zone of cathode polarization with a corresponding increase in the area of transverse section of the mandible and atrophy of the bone under the anode, all this causing pronounced asymmetry of the jaw bones. Microscopic changes in the bone were adequate to the macroscopic and characterized by sharp activation of its apposition (under cathode) and resorption (under anode).

Alloys↗

The mechanisms of the vulnerable window: the role of virtual electrodes and shock polarity.

Vulnerability and defibrillation are mechanistically dependent upon shock strength, polarity, and timing. We have recently demonstrated that shock-induced virtual electrode polarization (VEP) may induce reentry. However, it remains unclear how the VEP mechanism may explain the vulnerable window and polarity dependence of vulnerability. We used a potentiometric dye and optical mapping to assess the anterior epicardial electrical activity of Langendorff-perfused rabbit hearts (n = 7) during monophasic shocks (+/-100 V and +/-200 V, duration of 8 ms) applied from a transvenous defibrillation lead at various coupling intervals. Arrhythmias were induced in a coupling interval and shock polarity dependent manner: (i) anodal and cathodal shocks induced arrhythmias in 33.2 +/- 30.1% and 53.1 +/- 39.3% cases (P < 0.01), respectively, and (ii) the vulnerable window was located near the T-wave. Optical maps revealed that VEP was also modulated by the coupling interval and shock polarity. Recovery of excitability produced by negative polarization, known as de-excitation, and the resulting reentry was more readily achieved during the relative refractory period than the absolute refractory period. Furthermore, anodal shocks produced wavefronts propagating in an inward direction with respect to the electrode, whereas cathodal shocks propagated in an outward direction. Wavefronts produced by anodal shocks were more likely to collide and annihilate each other than those caused by cathodal shocks. The probability of degeneration of the VEP-induced phase singularity into a sustained arrhythmia depends upon the gradient of VEP and the direction of the VEP-induced wavefront. The VEP gradient depends upon the coupling interval, while the direction depends upon shock polarity; these factors explain the vulnerable window and polarity-dependence of vulnerability, respectively.

Action Potentials↗

Anodal excitation of intact peripheral nerves in humans.

The median nerves of six normal subjects were electrically stimulated at different locations on the wrist in a bipolar fashion. The evoked compound sensory nerve action potentials (CSNAPs) were recorded at the index finger. Electrical stimuli consisted of constant-current monophasic rectangular pulses. Initially, the nerve was stimulated with a cathodal current and a just supramaximal CSNAP was obtained. Then, at the same stimulus location, the nerve was excited with an anodal current. A just supramaximal response in the anodal-CSNAP was obtained, or until a maximum current of 100 mA was delivered. CSNAPs obtained from anodal excitation required several times more electrical stimulus intensity when compared to those derived from cathodal stimulation. Morphologically, they were similar, except the onset latency of the anodal-CSNAPs was approximately 0.2 to 0.3 msec early compared to that derived from cathodal stimulation. This implies that during anodal excitation, the site of nerve depolarization was not located underneath the anode, but was situated at some distance from it. Also, it appears that a minimum nerve length (10 mm or more) should be exposed to the anodal current in order to induce depolarization. A very localized application of the anodal stimulus often failed to elicit nerve depolarization.

Action Potentials↗

Simultaneous nitrification and denitrification in a single reactor using bio-electrochemical process.

Feasibility of a bio-electrochemical process for simultaneous nitrification and denitrification in a single reactor was experimentally investigated. The reactor consisted of anodic and cathodic electrodes, on which nitrifying and denitrifying biofilms, respectively, were fixed. Effects of the applied electric current and DO concentration in the bulk solution were examined. The TN removal could be achieved through the occurrence of nitrification and denitrification in anodic and cathodic biofilms, respectively. Both nitrification and denitrification rates increased with an increase in the applied electric current. Even at low DO concentration in the bulk solution, nitrification proceeded at a high rate by utilizing oxygen generated on the anode. Denitrification rate remained relatively high at high DO concentration due to supplying hydrogen gas to the inner side of the cathodic biofilm. The higher TN removal rate tended to be obtained at lower DO concentration and higher current density. From these results, it was concluded that the bio-electrochemical process was applicable to simultaneous nitrification and denitrification due to stable formation of aerobic and anoxic regions in the single reactor.

Bacteria, Aerobic↗

[Study on electrochemical degradation of acid red B(ARB)].

The electrochemical degradation of acid red B (ARB) with hydrogen peroxide and hypochlorite ion electrogenerated by paired electrooxidation technology was investigated. High performance liquid chromatography (HPLC) was used to inspect the degradation process of ARB. Through analyzing chromatographic survey and UV-Vis spectra, as well as the removal of CODCr, TOC and color in the anode and cathode cells, the degradation processes of ARB in different cells were different. The color removal in the cathode cell was slower than in the anode cell, but the CODCr and TOC removal, which were 71.70% and 56.40% respectively, was higher than the removal in the anode cell, which were 25.15% and 27.57%. It maybe result from the different oxidation capabilities of the electrogenerated substances in the anode and cathode cells.

Electrochemistry↗

[Measurement of rotational temperature in N2 DC glow discharge by optical emission spectroscopy].

Measurements of rotational temperature as low as several hundred Kelvin have been achieved using optical emission spectroscopy (OES) in nitrogen DC glow discharge. The strongest band of the first negative system of nitrogen molecule ion was chosen to determine the rotational temperature of nitrogen DC glow discharge at 4 different positions in the discharge area: back of the cathode; cathode sheath; positive column and anode glow region. In positive column the rotational temperature of N2+ increases apparently with the increasing discharge voltage from 500-1,100 V when the pressure is 10 Pa. However at pressure of 20 Pa the rotational temperature in positive column increases slightly with the increase of discharge voltage. On the contrary, the rotational temperature in cathode sheath takes reverse tendency when the discharge voltage varies from 500-1,100 V. As regard the anode glow region, the rotational temperature at 10 Pa decreases with the increase of discharge voltage, but that at the 20 Pa increases. We attribute the different changing tendencies of the rotational temperature to the different discharge status at different pressure. When the discharge voltage varies from 500 to 1,100 V, the discharge at pressure of 10 Pa is normal glow and that at 20 Pa is abnormal glow.

Electricity↗

[The emission of rare earth complex Eu(asprin)3phen].

Two kinds of electroluminescent devices were fabricated by doping the rare earth complex Eu(asprin)3phen into polymer PVK: (1) ITO/PVK:RE/LiF/Al; (2) ITO/PVK:RE/PBD/LiF/Al. A great difference in the EL spectrum was found between the two kinds of devices. In device (2) the intensity of 594 nm was rather weak compared with that of 614 nm. The spectrum was consistent with the photoluminescence (PL) spectrum under the state of thin film. But in device (1), the peak emission of 594 nm was comparable to that of 614 nm. Preliminary discuss on this phenomenon was made; in device (1), the recombination region was close to the metal cathode, effect of metal cathode on the electroluminescence of the rare earth complex caused the changes of the EL emission which was quite different from the TL emission. The phenomenon was not observed in device (2) whose recombination region was far from the cathode because an electron-transport layer was inserted.

Chelating Agents↗

Application of a bio-electrochemical reactor process to direct treatment of metal pickling wastewater containing heavy metals and high strength nitrate.

The fundamental performance of a bio-electrochemical reactor for the direct treatment of metal pickling wastewater was investigated experimentally. In the reactor, carbon anode and cathode were installed. On the cathode, denitrifying microorganisms were immobilized. Continuous experiments were carried out by feeding a synthetic wastewater containing nitrate and binary heavy metal ions, copper and lead, under different operating conditions. Acetate as well as the electric current was supplied at the minimum amount for stoichiometry of the dissimilatory denitrification reaction. The results indicated that the dissolved copper and lead removal, denitrification and neutralization could be achieved simultaneously in a single bio-electrochemical reactor. The dissolved heavy metals were removed by electrochemical deposition on cathode and by the other phenomena such as the formation of insoluble suspensions and the sorption on suspended bacterial sludge. Denitrification proceeded effectively with the utilization of both added acetate and hydrogen gas generated by electrolysis of water. The pH value increased up to around neutral due to the occurrence of denitrification in the reactor, although the influent pH was less than 3. The removal efficiencies of heavy metals and nitrate increased with increasing the current density. The applied electric current was indispensable for sustaining the stable treatment in the reactor.

Acetates↗

[Microbore liquid chromatography with dual electrode electrochemical detection of monoamine transmitters in brain microdialysates].

In the present work, the method of microbore liquid chromatography(MLC) with dual electrode electrochemical detection (DEED) was used to determine the monoamine transmitters and their metabolites in the striatal microdialysates from the anaesthetized rats. The potentials applied on the upstream (anodic) electrode and downstream (cathodic) electrode were set at +0.72V and +0.05V versus an Ag/AgCl reference electrode respectively. The interference of the large early-eluting peaks from brain dialysate was well eliminated on cathodic detection on the basis of electrochemical reversibility of catechol compounds. The collection efficiency of catecholamine (NA, A and DA) and DOPAC, that is the ratio of their responses in downstream electrode to those in upstream, was found to be in the range of 0.690 to 0.768, thereby providing reliable identification and measurement of early elutes. MLC-DEED is one of the best methods for the determination of monoamine transmitters at trace level. To optimize separation and detection, these adaptations were made to the system with respect to the injection valve, flow rate of the pump, connections between injector, column and detector, and cell volume of the detector. The detection limit could reach 1pg or less per injection, and the amounts, at least in the range of 2-200pg, were linearly correlated with the peak areas both at anodic detection and at cathodic detection. Prior to the collection of samples the probe recovery was measured in vitro at room temperature, and the recovery (%) for NA, DA, DOPAC, 5-HIAA, 5-HT and HVA were 19.5, 18.9, 22.1, 14,6, 16.5 and 19.3 respectively. The reported concentration of each compound was corrected according to probe recovery. The basal concentration of DA and 5-HT in striatal microdialysates was 12.5 +/- 1.8 and 5.0 +/- 0.7nmol/L. The perfussion of high K+ (100 mmol/L) through the dialysis probe induced a large increase of the concentration of NA, DA and 5-HT in microdialysates, and further increase of the concentration was observed in rat postmortem. The critical points for MLC-DEED are briefly discussed.

Animals↗

[The use of direct current in the local destruction of cancer tissues].

Two platinum electrodes were inserted into malignant cancer tissue. One electrode was positive or anode, and the other was negative or cathode. Five to thirty milliamperes were employed between two electrodes. The tissue impedance was initially 600 ohms and decreased to 300 ohms in 30 minutes following the start. Marked acidosis was obtained around the anode, while strong alkalosis was created around the cathode. Cancer tissues of 2cm in diameter around the electrode became necrotic in 60 min. This principle was applied for the local destruction of cancer tissues. Repeated use of direct current seemed to be effective in decreasing the cancer volume around electrodes. For more complete destruction of the cancer tissues, bleomycin was injected intravenously in experimental animals. Since the agent was positively charged, it was easily drawn toward the negative electrode. Direct current was applied following the bleomycin injection, and animal tissues around electrodes were examined. The drug was found to accumulate around the cathode in 6 out of eleven cases. The use of direct current might be helpful in accumulating anti-cancer drugs in malignant tissue.

Adult↗

Detection and quantification of circulating antigen in schistosomiasis by monoclonal antibody. II. The quantification of circulating antigens in human schistosomiasis mansoni and haematobium: relationship to intensity of infection and disease status.

Circulating cathodic and circulating anodic antigens were quantified in sera of patients infected with S. mansoni, S. haematobium or both parasites. A monoclonal antibody and a polyclonal antiserum were applied in precipitation and solid phase immunosorbent techniques using radio- and enzyme-labelled antibody as a tracer to detect the cathodic and anodic antigen respectively. The results show that circulating cathodic antigen can frequently be detected in an immunoprecipitation or an immunoradiometric assay in serum of infected patients. The serum concentration of this antigen was found to be significantly correlated to the number of S. mansoni worms and to be higher in patients with the hepatosplenic form of the disease than in those without such complications. Examining paired serum samples before and after specific treatment the determination of this antigen by monoclonal antibody reliably indicated efficacy of chemotherapy in patients having received different forms of treatment.

Adolescent↗

Crossed immunoelectrophoresis of human platelet membranes. Effect of charge on association and dissociation of the glycoprotein GPIIb-GPIIIa membrane complex.

The mechanism of association of the human platelet membrane GPIIb-GPIIIa-Ca2+ complex was studied by treating solubilized membranes with various enzymes and cationic peptides and by studying the binding of 45Ca2+ and 125I-fibrinogen before and after dissociation with EGTA and association with Ca2+. Neuraminidase shifted the complex cathodally (presumably due to cleavage of negatively charged domains), whereas trypsin had no such effect. The EGTA-dissociated complex was almost completely reassociated with neuraminidase or the cationic peptide, tetralysine. The monoclonal antibody 10E5, which specifically binds to the Ca2+-associated complex (not to its dissociated components), also bound to the neuraminidase-associated complex. Thus, Ca2+ is not necessary for the association of the complex. Neuraminidase treatment of washed intact platelets resulted in a cathodal shift of the membrane Triton X-100-extracted associated complex with no effect on its ability to dissociate in the presence of EGTA. Neuraminidase treatment of ADP-perturbed washed platelets also resulted in a cathodal shift of the associated complex; however, dissociation with EGTA was inhibited. Thus, critical neuraminidase-sensitive components of the complex (sialic acid residues) are not exposed on the surface of the platelet membrane of resting platelets, but do become accessible following platelet stimulation with ADP or membrane solubilization with Triton X-100. 45Ca2+ bound to the associated complex, to GPIIb of the dissociated complex (not to GPIIIa), to the Ca2+-reassociated complex, and to the neuraminidase-associated complex which had been dissociated with EGTA. Thus, neuraminidase-sensitive components of the solubilized membrane are not required for Ca2+ binding. 125I-fibrinogen bound to the associated complex (not the dissociated complex), to the Ca2+-reassociated complex, and to the neuraminidase-reassociated complex which had been dissociated with EGTA. Thus, Ca2+ is not necessary for 125I-fibrinogen binding to the major antigen complex.

Adenosine Diphosphate↗

Histological studies of electrically induced intramedullary callus.

The author studied the early changes of electrically stimulated bone marrow and carried out histological examinations. A constant current of 10 microAmp was delivered to the cathode which was placed in the humerus of each rabbit. On the 5th, 14th and 21 st day, the rabbits were killed, and the intramedullary tissues around the tip of the cathode were processed for light and electron microscopic observations. In the early stages after electrical stimulation, the leakage of erythrocytes, membranocystic degeneration of lipid cells, and proliferation of undifferentiated mesenchymal cells with moderately developed rER and collagen bundles were recognized. These findings indicate that the oxygen tension around the cathode was diminished in advance of the electrically stimulated callus formation. After prolonged electrical stimulation, both membranous and endochondral ossifications were more active than those in the control group.

Animals↗

Long-term surface stimulation of the cerebellum in the monkey. II. Electron microscopic and biochemical observations.

Phase and electron microscopy were used to study the effects of chronic intermittent or continuous stimulation applied to the surface of the cerebellum with bipolar platinum electrodes in monkeys. Damage under the anodes consisted of swelling of neuropil, variable loss of Purkinje cells, and a variable increase in fibrous glial processes. Under the cathode there was marked loss of Purkinje cells, thinning of the molecular layer, moderate swelling, occasional phagocytes with lipofuscin granules, and often an increase of fibrous glial processes. Despite the damage, normal appearing synaptic terminals remained in all layers under both anode and cathode, though sparser in fibrotic areas Gamma-aminobutyric acid (GABA) concentrations were decreased beneath the cathodes, reflecting the loss of Purkinje cells and other GABA-containing cells, and spermidine concentrations were increased in areas with increased fibrous glial processes.

Animals↗