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Vitamin C Enhances Iron Adsorption

Atanassova B.D., Tzatchev KN (2008). Ascorbic acid–important for iron metabolism. Folia Med ( Plovdiv). Oct-Dec; 50(4):11-6.

Ascorbic acid is actively involved in the control of iron metabolism. It has long been known to enhance absorption of iron from test meals. At first this effect was ascribed to luminal reduction and solubilsation of iron. Later, molecular cloning of mammalian duodenal brush-border reductase activity and studies in animals and man strongly supported ascorbate as the intracellular electron donor for duodenal ferri-reductase activity and provided molecular mechanism for an intracellular role of ascorbate in intestinal iron absorption. Factors that alter duodenal ascorbate levels (dietary intake of ascorbate, dehydroascorbate, or oxidants) may therefore alter the rate of absorption. Ascorbate could play dual role in human cells; it could react as pro-oxidant and as antioxidant. The balance of these contradictory effects depends on ascorbate concentration. Pro-oxidant reactions predominate at low concentrations; at higher concentrations vitamin C reacts as antioxidant. The increase of plasma ascorbate in human iron deficiency, especially in females in active age, could explain gender-related biological variation of plasma levels of vitamin C. The possible participation of ferric reductase activity Dcytb in transferrin cycle in liver and in neutrophil host defense implies new aspects of the role of vitamin C in the regulation of iron homeostasis.


Teucher B, Olivares M, Cori H (2004). Enhancers of iron absorption: ascorbic acid and other organic acids. Int J Vitam Nutr Res. Nov; 74(6):403-19.

Ascorbic acid (AA), with its reducing and chelating properties, is the most efficient enhancer of non-heme iron absorption when its stability in the food vehicle is ensured. The number of studies investigating the effect of AA on ferrous sulfate absorption far outweighs that of other iron fortificants. The promotion of iron absorption in the presence of AA is more pronounced in meals containing inhibitors of iron absorption. Meals containing low to medium levels of inhibitors require the addition of AA at a molar ratio of 2:1 (e.g., 20 mg AA: 3 mg iron). To promote absorption in the presence of high levels of inhibitors, AA needs to be added at a molar ratio in excess of 4:1, which may be impractical. The effectiveness of AA in promoting absorption from less soluble compounds, such as ferrous fumarate and elemental iron, requires further investigation. The instability of AA during food processing, storage, and cooking, and the possibility of unwanted sensory changes limits the number of suitable food vehicles for AA, whether used as vitamin fortificant or as an iron enhancer. Suitable vehicles include dry-blended foods, such as complementary, precooked cereal-based infant foods, powdered milk, and other dry beverage products made for reconstitution that are packaged, stored, and prepared in a way that maximizes retention of this vitamin. The consumption of natural sources of Vitamin C (fruits and vegetables) with iron-fortified dry blended foods is also recommended. Encapsulation can mitigate some of the AA losses during processing and storage, but these interventions will also add cost. In addition, the bioavailability of encapsulated iron in the presence/absence of AA will need careful assessment in human clinical trials. The long-term effect of high AA intake on iron status may be less than predicted from single meal studies. The hypothesis that an overall increase of dietary AA intake, or fortification of some foods commonly consumed with the main meal with AA alone, may be as effective as the fortification of the same food vehicle with AA and iron, merits further investigation. This must involve the consideration of practicalities of implementation. To date, programs based on iron and AA fortification of infant formulas and cow’s milk provide the strongest evidence for the efficacy of AA fortification. Present results suggest that the effect of organic acids, as measured by in vitro and in vivo methods, is dependent on the source of iron, the type and concentration of organic acid, pH, processing methods, and the food matrix. The iron absorption-enhancing effect of AA is more potent than that of other organic acids due to its ability to reduce ferric to ferrous iron. Based on the limited data available, other organic acids may only be effective at ratios of acid to iron in excess of 100 molar. This would translate into the minimum presence/addition of 1 g citric acid to a meal containing 3 mg iron. Further characterization of the effectiveness of various organic acids in promoting iron absorption is required, in particular with respect to the optimal molar ratio of organic acid to iron, and associated feasibility for food application purposes. The suggested amount of any organic acid required to produce a nutritional benefit will result in unwanted organoleptic changes in most foods, thus limiting its application to a small number of food vehicles (e.g., condiments, beverages). However, fermented foods that already contain high levels of organic acid may be suitable iron fortification vehicles.

Legal notice: The patent-pending EPO-BOOST® formula is proprietary to Biomedical Research Laboratories, LLC. Biomedical Research Laboratories, LLC has been successful in defending its intellectual property and prosecuting all unauthorized uses or violations to the fullest extent of both domestic and international law.

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