Deferration using anguibactin siderophore
AssigneeThe State of Oregon Acting by and through the State Board of Higher Education on Behalf of Oregon Health Sciences University
InventorJorge H. Crosa
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AssigneeThe State of Oregon Acting by and through the State Board of Higher Education on Behalf of Oregon Health Sciences University
InventorJorge H. Crosa
Estimating the term…
Methods for removing ferric iron from aqueous liquids and for performing deferration therapy are disclosed, involving the use of a novel siderophore, termed anguibactin. Anguibactin is isolated from a marine pathogen, Vibrio anguillarum, containing the pMJ1 plasmid. Anguibactin inhibits iron uptake by living cells, wrests iron from vertebrate tissues, removes iron from other siderophores and ferric hydroxide, and removes ferric iron from aqueous solutions, including cell-culture media. For deferration therapy, anguibactin from which bound iron has been removed is administered by dissolving in water or other liquid aqueous pharmaceutical carrier at a dosage typical for other siderophores. Anguibactin is preferably administered intramuscularly or subcutaneously, but can be given intravenously. Oral administration is also possible, particularly if the siderophore is encapsulated in a form allowing it to pass intact through the acidic environment of the stomach but become available for absorption in the intestine. This siderophore has the advantages of low molecular weight, extremely high affinity for ferric iron, and non-use by any known human pathogen. The structure is amenable to immobilization on a solid substrate.
A method for inhibiting the uptake of ferric iron by a population of living eukaryotic animal cells that is in contact with an aqueous medium comprising ferric iron, the method comprising:
A method for reducing the concentration of ferric iron present in a vertebrate animal subject, the method comprising:
A method for reducing the concentration of ferric iron present in the body of a vertebrate animal subject, comprising orally administering at least one pharmacologically effective dose of anguibactin that has been treated in a manner serving to protect the anguibactin from hydrolysis under acid conditions and make the anguibactin available for absorption into the body of said animal subject under neutral and alkaline conditions.
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