PubMed Health⌕ Search

PubMed · 6582549

[Round table. Electrosurgery in daily practice].

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

G Bouchier, M Cohen, P David, F Gombeaud, J Raulo, B Touati, M Vignon. [Round table. Electrosurgery in daily practice].. https://pubmed.ncbi.nlm.nih.gov/6582549/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Determination of tartaric acid in wines by FIA with tubular tartrate-selective electrodes.

A flow injection analysis (FIA) system comprising a tartrate-(TAT) selective electrode has been developed for determination of tartaric acid in wines. Several electrodes constructed for this purpose had a PVC membrane with a complex of quaternary ammonium and TAT as anion exchanger, a phenol derivative as additive, and a more or less polar mediator solvent. Characterization of the electrodes showed behavior was best for membranes with o-nitrophenyl octyl ether as solvent. On injection of 500 microL into a phosphate buffer carrier (pH = 3.1; ionic strength 10(-2) mol/L) flowing at 3 mL/min, the slope was 58.06 +/- 0.6 with a lower limit of linear range of 5.0 x 10(-4) mol/L TAT and R2 = 0.9989. The interference of several species, e.g. chloride, bromide, iodide, nitrate, gallic acid, tannin, sucrose, glucose, fructose, acetate, and citrate, was evaluated in terms of potentiometric selectivity coefficients. The Hofmeister series was followed for inorganic species and the most interfering organic ion was citrate. When red and white wines were analyzed and the results compared with those from an independent method they were found to be accurate, with relative standard deviations below 5.0%.

Electrodes↗

Rotating electrode potentiometry: lowering the detection limits of nonequilibrium polyion-sensitive membrane electrodes.

A rotating electrode configuration is evaluated as a means to lower the detection limits of newly devised polyion-sensitive membrane electrodes (PSEs). Planar potentiometric polycation and polyanion PSEs are prepared by incorporating tridodecylmethylammonium chloride and calcium dinonylnaphthalenesulfonate, respectively, into plasticized PVC or polyurethane membranes and mounting disks of such films on an electrode body housed in a conventional rotating disk electrode apparatus. Rotation of the PSEs at 5000 rpm results in an enhancement in the detection limits toward heparin (polyanion) and protamine (polycation) of at least 1 order of magnitude (to 0.01 unit/mL for heparin; 0.02 microg/mL for protamine) over that observed when the EMF responses of the same electrodes are assessed using a stir-bar to achieve convective mass transport. A linear relationship between omega(-1/2), where omega is the rotating angular frequency, and C1/2, the polyion concentration corresponding to half the total maximum deltaEMF response toward the polyion species, is observed. It is further shown that the rotating polycation sensor can be used as an end-point detector to greatly enhance (relative to nonrotated indicator electrode) the analytical resolution and precision for measurement of low concentrations of heparin when such samples are titrated with protamine. The theoretical basis for lowering the detection limits by rotating PSEs is discussed based on the unique nonequilibrium response mechanism of such sensors.

Electrodes↗

Ion-selective piezoelectric sensor for niacinamide assay in serum and urine.

An ion-selective piezoelectric (ISP) sensor was successfully applied for the determination of niacinamide in serum and urine. By coating a polyvinylchloride membrane containing niacinamide-silicotungstate on one electrode of a thickness-shear mode piezoelectric quartz crystal, the ISP device can adsorb niacinamide selectively. The amount of coating applied to the crystal was calculated from the Sauerbrey equation by monitoring the frequency change. The logarithm of the frequency shift was linear with the logarithm of niacinamide concentration over the range from 1.0 x 10(-9) to 1.0 x 10(-3) M with a detection limit of 1.0 x 10(-9) M at pH 7.0. Influencing factors were investigated and optimized. The results for real samples obtained by the proposed method were in good agreement with those obtained by the conventional methods.

Electrodes↗