Toxicological evaluation of some food additives including anticaking agents, antimicrobials, antioxidants, emulsifiers and thickening agents WHO FOOD ADDITIVES SERIES NO. 5 The evaluations contained in this publication were prepared by the Joint FAO/WHO Expert Committee on Food Additives which met in Geneva, 25 June - 4 July 19731 World Health Organization Geneva 1974 1 Seventeenth Report of the Joint FAO/WHO Expert Committee on Food Additives, Wld Hlth Org. techn. Rep. Ser., 1974, No. 539; FAO Nutrition Meetings Report Series, 1974, No. 53. ISOASCORBIC ACID AND ITS SODIUM SALT Explanation These compounds have been evaluated for acceptable daily intake by the Joint FAO/WHO Expert Committee on Food Additives (see Annex 1, Ref. No. 6) in 1961. The previously published monograph has been revised and is reproduced in its entirety below. BIOLOGICAL DATA BIOCHEMICAL ASPECTS Isoascorbic acid is readily absorbed and metabolized. Following an oral dose of 500 mg of isoascorbic acid to human subjects the blood level curves for ascorbic acid and isoascorbic acid showed a similar rise. In five human subjects, an oral dose of 300 mg was shown to have no effect on the urinary excretion of ascorbic acid (Kadin & Osadca, 1959). Isoascorbic acid was found to have no antagonistic effect on the action of ascorbic acid (Gould, 1948). TOXICOLOGICAL STUDIES Acute toxicity No information available. Short-term studies Rat Groups of 10 male rats were fed for 36 weeks on diets containing 1% of isoascorbic acid, and on diets without isoascorbic acid. There was no difference between the treated rats and the controls with respect to rate of growth and mortality. Gross post mortem examination and microscopic studies of various organs revealed no lesion attributable to isoascorbic acid (Fitzhugh & Nelson, 1946). Long-term studies Rat Groups of rats were fed on diets containing 1% of isoascorbic acid and diets without isoascorbic acid for two years. The growth rate, mortality, and histopathology were not affected by the treatment (Lehman et al., 1951). Comments: There are adequate short and long-term studies in the rat. The biochemical studies indicate that isoascorbic acid is readily metabolized and does not affect the urinary excretion of ascorbic acid. EVALUATION Level causing no toxicological effect Rat: 10 000 ppm (1%) in the diet equivalent to 500 mg/kg bw. Estimate of acceptable daily intake for man 0-5 mg/kg bw. REFERENCES Fitzhugh, O. G. & Nelson, A. A. (1946) Proc. Soc. exp. Biol., 61, 195 Gould, D. S. (1948) Arch. Biochem., 19, 1 Kadin, H. & Osadca, M. (1959) J. Agric. Food Chem., 7, 358 Lehman, A. J. et al. (1951) Advanc. Food Res., 3, 197
See Also: Toxicological Abbreviations