Determination of oxalic acid in urine by atomic absorption spectrophotometry

1976 ◽  
Vol 70 (1) ◽  
pp. 71-77 ◽  
Author(s):  
C. Koehl ◽  
J. Abecassis
1974 ◽  
Vol 20 (11) ◽  
pp. 1444-1445 ◽  
Author(s):  
R Menachè

Abstract The method of Gitelson et al. was modified to a microscale procedure and adapted for atomic absorption spectrophotometry. Oxalic acid in urine is precipitated with excess of calcium ions at pH 5. The excess of calcium present in the supernate and the total calcium added and present in the urine at pH 2 are determined by atomic absorption spectrophotometry. The oxalic acid present in the precipitate is calculated indirectly from the difference between the two determinations of calcium. This method is useful for routine determination of urinary oxalic acid.


1965 ◽  
Vol 48 (6) ◽  
pp. 1100-1103
Author(s):  
C H Mcbride

Abstract The atomic absorption method studied last year was re-examined and extended to include calcium and sodium. The procedures were submitted to 16 collaborators for determination of Ca, Cu, Fe, Mg, Mn, Na, and Zn. Results for Ca and Na were discouraging; further study is recommended.


1979 ◽  
Vol 62 (1) ◽  
pp. 153-159
Author(s):  
Luis F Corominas ◽  
Victor M Boy ◽  
Manuel Guijosa

Abstract The official first action AOAC method for the spectrophotometric determination of biuret in urea, 2.072—2.074, was compared with official first action AOAC method 2.C01-2.C03 (atomic absorption spectrophotometry), 2 simplified versions of 2.072-2.074, and modified versions of 2 alternative procedures of the International Organization for Standardization. Three synthetic urea samples (0.3, 1.4, and 3.0% biuret) and 1 commercial urea sample (1.0% biuret) were analyzed. The methods proved to be equivalent and none showed a definite advantage over 2.072-2.074. The purification of biuret and the interference by ammonia are also discussed.


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