scholarly journals The specific conductivity of solutions of oxyhæmoglobin

When preparing a paper on the mechanism of hæmolysis two or three years ago my attention was accidentally called to a statement in a paper by the late Prof. A. Gamgee in the ‘Proceedings’ of the Royal Society, that “although solutions of oxyhæmoglobin possess a low conductivity this is very much higher than has been found in the previous observations of Stewart.” In a note appended to my paper I suggested that this could only mean “that either his (Gamgee’s) oxyhæmoglobin or his distilled water was less thoroughly freed from electrolytes than mine. In observations of this kind the error must appear as too high and not as too low a conductivity.” Prof. Gamgee having laid stress on the purity of his distilled water and oxyhæmoglobin, this result seemed very puzzling, all the more as my object in determining the conductivity of some specimens of oxyhæmoglobin was merely to control their suitability for addition to blood in the determination of the relative volume of corpuscles and plasma by a colorimetric method described in the paper, and no such effort has been made to carry the exclusion of foreign electrolytes to the practically possible limit as would have been deemed indispensable had the conductivity of hæmoglobin been investigated for its own sake.

Author(s):  
F. A. J. Armstrong

Silicon in sea water may be present in suspension, in particles of clay or sand, as a constituent of diatoms, etc., or in solution. Some silicon in solution occurs in the form of silicate. This is usually estimated by the colorimetric method of Diénert & Wandenbulcke (1923), which makes use of the yellow colour of the silicomolybdic acid which is formed when ammonium molybdate and sulphuric acid are added to the water (Atkins, 1923). The colour may be compared with that of standard solutions of picric acid (Diénert & Wandenbulcke, 1923) or potassium chromate (Swank & Mellon, 1934). The method is simple but the colour in sea water is often faint and is not easy to match visually, nor is its intensity strictly proportional to the concentration of silicate. Less colour is produced in sea water than in standard solutions made with distilled water and this ‘salt error’ must be allowed for (Brujewicz & Blinov, 1933; Wattenberg, 1937; Robinson & Spoor, 1936).


1990 ◽  
Vol 10 (1) ◽  
pp. 89-92 ◽  
Author(s):  
Liliane Larpent ◽  
Christian Verger

The fate of the peritoneal membrane on continuous ambulatory peritoneal dialysis (CAPD) is usually evaluated through the modification of its permeability to various solutes as glucose, creatinine, and urea. Therefore, the accuracy of the methods used for measurements of creatinine is of great importance. A particular problem does exist for creatinine determination as it may be influenced by the presence of glucose. We studied a new enzymatic colorimetric method for creatinine determination in peritoneal dialysis solutions which contain high dextrose concentrations. Creatinine was measured in plasma, urine, and dialysate from 18 patients on CAPD and in pure dextrose solutions, with an enzymatic test (Boehringer Mannheim) and with Jaffe's reaction on two different analyzers: Astra (Beckman) and Eris (Merck). Creatinine results were similar with both assays (Jaffe's reaction and enzymatic test) when measured in blood and urine. However the Jaffe's reaction gave higher creatinine results than the enzymatic test (p < 0.001), when assays were performed in peritoneal dialysis solutions and in pure glucose solutions. In addition, it appeared that other components of dialysis solutions, mainly calcium chloride, influenced unpredictably the results of creatinine with the Jaffe's reaction. We conclude that specific enzymatic test is a more accurate and reliable method to evaluate creatinine kinetics through the peritoneal membrane when determined in CAPD solutions.


1960 ◽  
Vol 53 (2) ◽  
pp. 263-265 ◽  
Author(s):  
H. V. Claborn ◽  
M. C. Ivey ◽  
H. D. Mann
Keyword(s):  

2021 ◽  
Author(s):  
Fariba Pourkarim ◽  
Elaheh Rahimpour ◽  
Maryam Khoubnasabjafari ◽  
Vahid Jouyban-Gharamaleki ◽  
Afshin Gharakhani ◽  
...  

1984 ◽  
Vol 67 (5) ◽  
pp. 861-862 ◽  
Author(s):  
John Morawski ◽  
Glenn Kyle

Abstract A rapid, reliable separation and quantitation of zoalene (3,5-dinitroo-toluamide) from feeds is accomplished by using reverse phase liquid chromatography (LC) and ultraviolet detection. An extraction technique which is similar to the present AOAC official colorimetric method is used before chromatographic analysis. This extraction is followed by an activated alumina cleanup and LC to separate zoalene from feed matrix. The methodology was applied to a variety of spiked feed matrices, and yielded good recoveries. Liquid chromatographic results were shown to correlate with colorimetric determinations.


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