scholarly journals NOTES ON THE DETERMINATION OF SERUM INORGANIC PHOSPHATE AND SERUM PHOSPHATASE ACTIVITY

1937 ◽  
Vol 120 (1) ◽  
pp. 167-175 ◽  
Author(s):  
Aaron Bodansky
1977 ◽  
Vol 23 (7) ◽  
pp. 1275-1280 ◽  
Author(s):  
H Baadenhuijsen ◽  
H E Seuren-Jacobs ◽  
A P Jansen

Abstract The merits of the vanadomolybdate method in the determination of inorganic phosphate are highly underestimated with regard to the simplicity of the method and the stability of both the reagents and the color that is formed. The absorption curve of the phosphovanadomolybdate complex, with its maximum at 335 nm, extends into the visible range of the spectrum. This permits measurements with inexpensive tungsten-lamp colorimeters. On-stream dialysis is best done in a nitric acid medium, 0.15 mol/liter. Paralleled by the change in the H2PO4-/H3PO4 ratio, appreciable protein binding and poor dialysis efficiency are seen at lower acid concentrations (pH greater than 1.0). Optimum reaction-mixture concentrations of vanadium and molybdenum appeared to be respectively 0.2 and 5 mmol/liter up to 3 mmol of phosphate per liter, in a final acid medium of 0.2 mol/liter, concentrations considerably lower than those used in some studies published earlier. Color development with the stable combined reagent is complete after only 20 s at room temperature and the color is stable for at least 2 h. Figures on precision and accuracy demonstrate the reliability of the method.


2011 ◽  
Vol 19 (1) ◽  
pp. 13-17
Author(s):  
Md Shahidul Haque ◽  
Zerin Fahmida Shima

To characterize serum constituents in blood in response to cold exposure, we measured serum inorganic phosphate (Pi) and alkaline phosphatase (ALP) levels. After 30 min exposure of cold, the serum Pi and alkaline phosphatase levels were 3.4 ± 0.06 mg/l and 72.33 ± 0.45 μmole/l respectively where as the control levels of these constituents are 3.05 ± 0.03 mg/l and 84 μmole/l respectively. Cold exposure for 30 min induces serum Pi concentration by 11.5 % and decreases ALP levels significantly by 13.9 % compared to control rats. Serum Pi for 1 h and 2 h were 3.8 mg/l and 4.17 ± 0.16 mg/l while ALP levels were 57.33 ± 0.88 μmole/l and 91 ± 1.73 μmole/l respectively in different groups of rats. Cold exposure stimulates serum Pi by 24.6 % and 36.7 % and reduces ALP activity by 31.7 % significantly and without significant change for 1 h and 2 h respectively. Another groups of rats exposed to cold for 4 h had Pi and ALP levels 4.66 ± 0.88 mg/l and 85.66 ± 0.88 μmole/l respectively. Cold exposure similarly stimulates Pi content significantly by 52.8 % without affecting ALP activity compared to the control rather reaches to basal level. Our results demonstrate that Pi and ALP levels in cold-exposed rats are regulated in different ways.   doi: 10.3329/taj.v19i1.3162 TAJ 2006; 19(1):13-17


1964 ◽  
Vol 10 (1) ◽  
pp. 75-82 ◽  
Author(s):  
H Keay ◽  
J A Trew

Abstract An automated procedure for the measurement of alkaline phosphatase activity by a modification of the Bodansky method is described. It has been possible to adapt the Fiske-SubbaRow method for phosphate so that alkaline phosphatase is determined by a second run, immediately following the determination of inorganic phosphate. Studies of the effect of time, pH, and concentration of barbital on the enzyme activity are discussed, and the advantages of the method are listed.


Author(s):  
R. Lawrence

Several current techniques for the determination of serum inorganic phosphate in the presence of proteins are shown to have important disadvantages. An improved manual micromethod is described in which proteins are kept in solution by the use of sodium lauryl sulphate and the phosphate determined by the molybdenum blue reaction. The procedure has been adapted for the Technicon AutoAnalyzer and the Vickers D-300 and M-300, and has been shown to give very good precision in routine use.


1976 ◽  
Vol 22 (11) ◽  
pp. 1909-1911 ◽  
Author(s):  
J E Carothers ◽  
N M Kurtz ◽  
J Lemann

Abstract Values for serum inorganic phosphate (Pi) concentrations in groups of healthy adults vary widely, the coefficient of variation ranging from 10 to 15%. We undertook to determine in 23 healthy adults whether part of this variation could be accounted for by (a) drawing blood in syringes vs. evacuated tubes (b) the time between blood sampling and separation of serum or plasma, and (c) the prevention of clotting. Values were unaffected by a, decreased significantly with time at room temperature between blood sampling and separation of cells in both serum and plasma, and were significantly lower in plasma than in serum. The group coefficient of variation for Pi averaged 13% and was uninfluenced by the blood-processing technique.


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