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Urea, estimation test

In the particular example shown, zinc sulfate and barium hydroxide are being dispensed into the test tube so as to precipitate the proteins. The filtrate obtained is the filtrate from 10 microliters of serum. This can be used for several purposes and in the application being referred to, an amount equivalent to 3 microliters is being used for sugar determination, by the hexokinase procedure and an amount equivalent to 3 microliters is being used for urea estimation with diacetylmonoxime (15). [Pg.105]

None of the exposures produced changes in clinical chemistry values (blood count, blood nitrate, blood urea nitrogen, serum enzymes, and serum electrolytes or urinalysis and nitrate and nitrite urinary excretion), spontaneous electrical activity of the cortex of the brain (detected by EEG), pulse rate and sinus rhythm, or pulmonary function. Visual and auditory acuity, exercise EKG, and time estimation tests did not differ from control values for any of the exposures. Only one of several cognitive tests was affected by exposure and the change occurred only in the four subjects exposed at 1.5 ppm. The test was taken during the time the subjects were experiencing severe headaches. [Pg.99]

The activity of enzymes in the film was estimated in the following way In order to test the activity of urease, we utilized a calorimetric assay based on urea hydrolysis the enzymatic reaction was followed at 590 nm, the suitable wavelength for bromcresol purple (Chandler 1982). Urea concentration was 1.67 ts 10 M. [Pg.158]

Cyanuric fluoride has been used to modify tyrosine residues, substituting the phenolic hydroxyl group. A maximum of 3 residues in RNase was found to react at pH 10.9 and 25° (148a). However, some mystery surrounds this number, as with other estimates of accessibility, since alkaline-denatured material where all tyrosine residues are available still showed the reaction of only 3 residues with cyanuric fluoride. However, similar observations have been made on iodination in 8 Af urea (11 )- At pH 9.3, Takenaka et al. (149) found that only 2 residues reacted and that 115 was not one of them. Two more reacted after alkali denaturation. Two were resistant under all conditions tested. No enzymic activity data were reported. [Pg.685]

While low serum cholesterol levels have been observed in malnourished patients, largely as a result of decreased synthesis of lipoproteins in the liver, hypocholesterolemia occurs later in the course of malnutrition and is therefore not useful as a screening test. PEM usually results in low serum urea nitrogen (BUN), urinary urea, and total nitrogen. Estimation of 24-h urine creatinine excretion is also a valuable biochemical index of muscle mass (when there is no impairment in renal function). The urinary CHI is correlated to lean body mass and anthropometric measurements. In edematous patients, for whom the extracellular fluids contribute to body weight and spuriously high body mass index values, the decreased CHI values are especially useful in diagnosing malnutrition. [Pg.258]

Formaldehyde-releasing preservatives, such as quater-nium-15, diazolidinyl urea, and imidazolidinyl urea, are widely used in cosmetics and topical medications and are well-known contact sensitizers. In spite of positive patch test reactions to these preservatives in a number of patients, only some of these patients will react when they use the corresponding commercial formulations. This is because the concentrations of preservatives in the commercial products are often below the threshold necessary to produce a clinical reaction. This finding confirms the importance of using commercial formulations of topical agents in estimating the clinical relevance of patch test results (10). [Pg.1441]

A reagent stick manufactured by Ames for the estimation of blood urea. The basis of the test is the hydrolysis of urea by urease to give carbon dioxide and ammonium ions. The latter causes a change in colour of a pH sensitive dye. [Pg.42]

A strip test manufactured by Warner for the estimation of blood urea. It is based on the action of urease on urea. The ammonia formed as a result changes the colour of an indicator dye. [Pg.362]

Nitrites, which appear in stale urine, interfere with the test by forming yellow nitro derivatives, which, unlike the urea pigment, are not bleached by addition of alkali. Sulphanilamide, which may appear in the urine after administration of one of the many forms of the drug, gives an intense red colour with the reagent, and thus may be estimated colorimetrically (A. E. Werner, 1938). [Pg.397]


See other pages where Urea, estimation test is mentioned: [Pg.71]    [Pg.459]    [Pg.125]    [Pg.9]    [Pg.26]    [Pg.596]    [Pg.528]    [Pg.465]    [Pg.502]    [Pg.70]    [Pg.189]    [Pg.1361]    [Pg.32]    [Pg.950]    [Pg.169]    [Pg.565]    [Pg.131]    [Pg.66]    [Pg.256]    [Pg.121]    [Pg.23]    [Pg.123]    [Pg.206]    [Pg.207]    [Pg.437]    [Pg.519]    [Pg.195]    [Pg.384]    [Pg.384]    [Pg.333]   
See also in sourсe #XX -- [ Pg.519 ]




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Urea, estimation

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