The pharmacokinetics and pharmacodynamics of iron preparations.

Article Details

Citation

Geisser P, Burckhardt S

The pharmacokinetics and pharmacodynamics of iron preparations.

Pharmaceutics. 2011 Jan 4;3(1):12-33. doi: 10.3390/pharmaceutics3010012.

PubMed ID
24310424 [ View in PubMed
]
Abstract

Standard approaches are not appropriate when assessing pharmacokinetics of iron supplements due to the ubiquity of endogenous iron, its compartmentalized sites of action, and the complexity of the iron metabolism. The primary site of action of iron is the erythrocyte, and, in contrast to conventional drugs, no drug-receptor interaction takes place. Notably, the process of erythropoiesis, i.e., formation of new erythrocytes, takes 3-4 weeks. Accordingly, serum iron concentration and area under the curve (AUC) are clinically irrelevant for assessing iron utilization. Iron can be administered intravenously in the form of polynuclear iron(III)-hydroxide complexes with carbohydrate ligands or orally as iron(II) (ferrous) salts or iron(III) (ferric) complexes. Several approaches have been employed to study the pharmacodynamics of iron after oral administration. Quantification of iron uptake from radiolabeled preparations by the whole body or the erythrocytes is optimal, but alternatively total iron transfer can be calculated based on known elimination rates and the intrinsic reactivity of individual preparations. Degradation kinetics, and thus the safety, of parenteral iron preparations are directly related to the molecular weight and the stability of the complex. High oral iron doses or rapid release of iron from intravenous iron preparations can saturate the iron transport system, resulting in oxidative stress with adverse clinical and subclinical consequences. Appropriate pharmacokinetics and pharmacodynamics analyses will greatly assist our understanding of the likely contribution of novel preparations to the management of anemia.

DrugBank Data that Cites this Article

Drugs
Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
Ferric cationTransferrin receptor protein 1ProteinHumans
Yes
Agonist
Details
Ferric derisomaltoseHemoglobin subunit alphaProteinHumans
Unknown
Binder
Details
Ferric derisomaltoseTransferrin receptor (Protein Group)Protein groupHumans
Unknown
Binder
Details
Ferrous sulfate anhydrousHemoglobin subunit alphaProteinHumans
Yes
Binder
Details
Ferrous sulfate anhydrousTransferrin receptor (Protein Group)Protein groupHumans
Yes
Substrate
Details
Tetraferric tricitrate decahydrateTransferrin receptor protein 1ProteinHumans
Yes
Ligand
Details
Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
Ferrous sulfate anhydrousCytochrome b reductase 1ProteinHumans
Unknown
Substrate
Details
Ferrous sulfate anhydrousSerotransferrinProteinHumans
Unknown
Substrate
Details
Drug Transporters
DrugTransporterKindOrganismPharmacological ActionActions
Ferrous sulfate anhydrousNatural resistance-associated macrophage protein 2ProteinHumans
Unknown
Substrate
Details
Drug Reactions
Reaction
Details