Spectrophotometric determination of vitamin D in presence of vitamin A

The Analyst ◽  
1964 ◽  
Vol 89 (1061) ◽  
pp. 534 ◽  
Author(s):  
R. K. Barua ◽  
M. V. K. Rao
1978 ◽  
Vol 61 (3) ◽  
pp. 735-745
Author(s):  
Ellen J De Vries ◽  
Frits J Mulder ◽  
Ben Borsje

Abstract The official first action method for determining vitamin D in multivitamin preparations was modified. The method was collaboratively studied by 7 laboratories, using 6 preparations in oil. The preparations consisted of vitamin D at various levels and at various ratios (in w/w) to vitamin A. Three samples contained cholecalciferol and 3 samples contained vitamin D3 from vitamin D3 resin. After outliers were eliminated by the Dixon test, data were analyzed and averages were compared with amounts of vitamin D known to be in each sample. For samples with vitamin D: vitamin A ratios of 1:0.5, 1:5, and 1:10, the mean vitamin D recoveries were 98.8, 94.6, and 90.7%, respectively. The method has been adopted as official final action.


1954 ◽  
Vol 26 (9) ◽  
pp. 1406-1409 ◽  
Author(s):  
D. T. Ewing ◽  
T. D. Schlabach ◽  
M. J. Powell ◽  
J. W. Vaitkus ◽  
O. D. Bird

Nature ◽  
1945 ◽  
Vol 155 (3941) ◽  
pp. 575-576
Author(s):  
W. S. METCALF

1978 ◽  
Vol 61 (3) ◽  
pp. 731-734
Author(s):  
Ellen J De Vries ◽  
Frits J Mulder ◽  
Ben Borsje

Abstract The official first action method for determining vitamin D in multivitamin preparations was modified. The method was collaboratively studied by 7 laboratories, using 6 preparations in oil. The preparations consisted of vitamin D at various levels and at various ratios (in w/w) to vitamin A. Three samples contained cholecalciferol and 3 samples contained vitamin D3 from vitamin D3 resin. After outliers were eliminated by the Dixon test, data were analyzed and averages were compared with amounts of vitamin D known to be in each sample. For samples with vitamin D: vitamin A ratios of 1:0.5, 1:5, and 1:10, the mean vitamin D recoveries were 98.8, 94.6, and 90.7%, respectively. The method has been adopted as official final action.


1940 ◽  
Vol 12 (11) ◽  
pp. 639-644 ◽  
Author(s):  
D. T. Ewing ◽  
J. M. Vandenbelt ◽  
A. D. Emmett ◽  
O. D. Bird

1979 ◽  
Vol 62 (3) ◽  
pp. 545-548
Author(s):  
Sayed M Hassan

Abstract The method of orthogonal functions has been applied to the rapid spectrophotometric determination of vitamin D in oily injections. The method involves saponification of the sample and extraction of the unsaponifiable matter with ether. After cautious evaporation of ether, the residue is dissolved in isopropanol and the absorbance of the solution is measured in the range 246–296 nm at 10 nm intervals. For BPC injections, the saponification step may be omitted. A suitable dilution of the sample in isopropanol is measured in the range 250.5– 300.5 nm at 10 nm intervals. Accurate and precise results are obtained in both cases.


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