Abstract:
An instrument for measuring coagulation parameters is provided in which plasma and at least one reagent are mixed by spinning in a cuvette with transparent windows and in which measurement is then made of scatter by the mixture of the energy of a light beam sent into the mixture. Upon spin, the plasma components and reagent are displaced into the chamber,thus determining the initiation of the presence of the mixture in which the clot forms, and a photodetecting unit senses the change in the energy of the scattered light, caused by clot formation.
Abstract:
An electrochemical cell for measuring the activity of one or more ionic species such as pNa, pK, pCa, pNH₄, pCl etc. consisting of two sensors selective to the actual ionic species, one of which is used as the reference electrode and the other as the measurement electrode. The two sensors are chosen preferably identical. The electrode used as the reference electrode is brought into contact with a solution of known ionic activity and an ionic strength which is greater, equal to or substantially greater than that of the unknown solution to be measured. The measurment electrode is brought into contact with the unknown solution to be measured, while a third electrode is used purely for instrumental reasons and does not participate in the measurement.
Abstract:
An instrument for measuring coagulation parameters is provided in which plasma and at least one reagent are mixed by spinning in a cuvette with transparent windows and in which measurement is then made of scatter by the mixture of the energy of a light beam sent into the mixture. Upon spin, the plasma components and reagent are displaced into the chamber,thus determining the initiation of the presence of the mixture in which the clot forms, and a photodetecting unit senses the change in the energy of the scattered light, caused by clot formation.
Abstract:
Description of a method for the potentiometric determination of the total calcium (II) content in biological fluids (serum, plasma and urine) based on dilution of the sample. The results obtained, when compared to the usual methods in current use, show the validity of the proposed method; furthermore, the pH of the buffer solution used for diluting the sample guarantees optimum operating conditions as well as long working life of the potentiometric sensing elements and maximum reliability when compared to other methods employing acidification of the sample.
Abstract:
A method for producing a liquid phase substance having a pre-established concentration of CO₂ suitable for calibrating analytical instruments such as hemogasanalyzers consists in:
preparing an aqueous solution of precisely known strength of a water-soluble salt of carbonic acid (bicarbonate or alkaline carbonate), then transferring said solution to a flow reactor containing a cation exchange resin in hydrogenionic form, passing the aforesaid solution of carbonic acid salt through the aforesaid cation resin, thereby achieving the reaction of producing a pre-established quantity of CO₂, and transferring the eluate thus obtained directly to the analytical instrument for calibration.
Abstract:
Electrodes for the measurement of pCO2 and/or pO2 are calibrated with an exposed aliquot of a calibration liquid. A constituent such as a ferrioxalate salt in the calibration liquid is converted to the gas in a reproducible concentration by exposure of the aliquot to light. In some instances, the calibration liquid is equilibrated with air prior to exposure. Some mechanisms of light generation of carbon dioxide also consume oxygen, so as to depress the pO2 value by a reproducible amount. The use of two different calibration liquids enables both one-point and two-point calibration of the Clark oxygen electrode and the Severinghaus pCO2 electrode of a blood gas instrument. Aqueous acidic ferrioxalate compositions are disclosed for use as calibrants of pCO2 and of pO2 after photodecomposition. Compositions with high iron(III) to oxalate molar ratios (e.g., 5:1 to 100:1 with 0.3 to 15 millimolar oxalate) produce carbon dioxide on exposure without oxygen consumption. Compositions with low iron(III) to oxalate ratios (e.g., 1:1000 to 1:2000) with 0.1 to 5 millimolar iron(III) produce carbon dioxide on exposure with concurrent oxygen consumption. Use of the two types of compositions enables calibration values to be established with varying pCO2 values and with, respectively, high and low pO2 values.