Eisenblatt examines how the trace element copper contributes to normal iron transport in the body according to scientifically reviewed EU claims.
Explore the guideIron is one of the best-known trace elements in the human body. It is a component of haemoglobin and enables oxygen transport in the blood. But iron alone is not enough — for it to travel from food into the cells, complex transport mechanisms are required, and other trace elements take part in them.
Iron transport describes the path of iron from absorption in the small intestine, through transfer into blood plasma, to distribution to target tissues such as bone marrow, liver, and muscle. Along this path, iron must repeatedly change its oxidation state — from the divalent (Fe²⁺) to the trivalent form (Fe³⁺) and back. These conversions require enzymes that depend on certain minerals as cofactors.
The European Food Safety Authority (EFSA) has produced scientific opinions on the contribution of copper to iron transport. On this basis, the EU Commission has published an authorised health claim.
The trace element copper has an EU-authorised health claim relating to normal iron transport in the body.
Copper is an essential trace element that takes part in numerous oxidative processes in the body. In connection with iron transport, copper is a component of the enzyme ceruloplasmin, a ferroxidase in blood plasma. This enzyme oxidises divalent iron (Fe²⁺) into trivalent iron (Fe³⁺) so that it can bind to the transport protein transferrin.
In accordance with Regulation (EU) No 432/2012
By quantity, iron is the most abundant trace element in the human body. In adults, total stores amount to roughly 3–5 g. About two thirds of that is found in the haemoglobin of red blood cells. The remaining amount is distributed across storage forms such as ferritin and functional enzymes in the liver, spleen, and bone marrow.
For iron to fulfil its tasks, it must be distributed purposefully throughout the body — a process in which copper-containing enzymes with a documented contribution take part.
Iron is involved in a wide range of physiological processes. Without functioning transport, supplying the tissues with this trace element would not be possible. In detail, this concerns:
As the body has no active excretion mechanism for iron, iron homeostasis is controlled mainly through the regulation of uptake and intracellular transport. Daily iron losses via the skin, intestinal epithelium, and minor bleeding amount to roughly 1–2 mg and must be replaced through the diet.
Copper fulfils its function in iron transport via two key enzymes. Ceruloplasmin, which circulates in blood plasma, is a multicopper ferroxidase that oxidises Fe²⁺ into Fe³⁺. Only in the trivalent form can iron bind to the plasma protein transferrin, which transports it to the target tissues.
Hephaestin, a membrane-bound homologue of ceruloplasmin, is located in the enterocytes of the small intestine. It catalyses the same oxidation reaction and thereby enables the export of iron from the intestinal cells into the blood. Both enzymes are copper-dependent — where copper intake is insufficient, their activity is limited.
Under EU regulation, the following authorised claim applies:
„Copper contributes to normal iron transport in the body“ — In accordance with Regulation (EU) No 432/2012
Copper is found in numerous foods. Particularly rich in copper are organ meats (especially liver), shellfish, nuts, seeds, legumes, and whole grain products. Dark chocolate and certain vegetables such as potatoes and mushrooms also provide notable amounts. The reference value for daily copper intake is 1 mg under EU Regulation 1169/2011.
The bioavailability of copper from food is usually between 30 % and 60 %. It is influenced, among other things, by the simultaneous consumption of zinc, vitamin C, and phytic acid, as these substances can compete with copper for absorption in the small intestine.
A detailed collection of information on copper and its documented contribution to normal iron transport — in accordance with EU regulation.
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