Quantitative Determination of FD&C Colors in Foods

1975 ◽  
Vol 58 (2) ◽  
pp. 278-282
Author(s):  
Charles Graichen

Abstract A published procedure using Amberlite LA-2 (a liquid anion exchange resin) solutions to extract colors from food and the salt solution cellulose chromatographic technique to separate colors from each other were updated and submitted to collaborative study. Three batches of cookies and 4 purchased products were analyzed by 13 collaborators. The 3 batches of cookies contained different color mixtures requiring the selection of various procedures. The 4 purchased products were selected principally to include a variety of foods. Some results were partially deficient. The deficiencies reflect certain inadequacies in the directions as written rather than basic flaws in the method. Some improvements were suggested by the collaborators. The Associate Referee recommends that the method be further revised to correct the present inadequacies and to include some improvements, and that the revised method be submitted to another collaborative study.

1969 ◽  
Vol 52 (4) ◽  
pp. 844-846
Author(s):  
Ernest B Beyer

Abstract In a revised procedure for the polarographic determination of thimerosal tincture and solution, a smaller diameter column containing less resin eliminated the problem of channeling and incomplete elution of thimerosal. The anion exchange resin provides sufficient cleanup so that direct comparison of sample and standard diffusion currents is possible instead of the standard addition technique originally specified. Recoveries for Thimerosal Tincture and Solution NF were 101 and 100%, respectively. The method is recommended for collaborative study.


1970 ◽  
Vol 53 (3) ◽  
pp. 621-623
Author(s):  
M Trop ◽  
I M Levinger

Abstract An analytical method for determination of α-hydroxy and α-keto acids is developed based on separation of the acids from other components by acidic alcoholic extraction and by adsorption on and elution from an anion exchange resin, followed by thin layer chromatography. Acids are identified by eerie ammonium nitrate reagent sprayed on the chromatogram. Quantitative determination is performed by manometric measurement of gas released in reaction with that reagent.


1962 ◽  
Vol 13 (3) ◽  
pp. 359-364 ◽  
Author(s):  
Dominic D. Dziewiatkowski

In autoradiograms of slices of costal cartilage, incubated for 4 hours in a salt solution containing S35-sulfate and then washed extensively and dehydrated, about 85 per cent of the radioactivity was assignable to the chondrocytes. From alkaline extracts of similarly prepared slices of cartilage, 64 to 83 per cent of the total sulfur-35 in the slices was isolated as chondroitin sulfate by chromatography on an anion-exchange resin. In view of the estimate that only about 15 per cent of the radioactivity was in the matrix, the isolation of 64 to 83 per cent of the total sulfur-35 as chondroitin sulfate is a strong argument that the chondrocytes are the loci in which chondroitin sulfate(s) is synthesized.


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