Claims for Patent: 8,815,301

Summary for Patent: 8,815,301

Title:	Stable iron oligosaccharide compound
Abstract:	The invention relates to an iron oligosaccharide compound with improved stability comprising a hydrogenated oligosaccharide in stable association with ferric oxyhydroxide, the content of dimer saccharide in said hydrogenated oligosaccharide being 2.9% by weight or less, based on the total weight of the hydrogenated oligosaccharide. In further aspects is provided a process for preparing said compound as well as the use of said compound for preparation of a composition for treatment of iron deficiency anaemia.
Inventor(s):	Andreasen; Hans (Holb.ae butted.k, DK)
Assignee:	Pharmacosmos Holding A/S (Holbaek, DK)
Application Number:	13/138,669
Patent Claims:	1. An iron oligosaccharide compound comprising a hydrogenated oligosaccharide in stable association with ferric oxyhydroxide, the hydrogenated oligosaccharide having a weight average molecular weight (Mw) between 500 and 3,000 Daltons, wherein the content of dimer saccharide in said hydrogenated oligosaccharide is 2.9% by weight or less, based on the total weight of the hydrogenated oligosaccharide, wherein the hydrogenated oligosaccharide is hydrogenated dextran having a number average molecular weight (Mn) above 500 Daltons, 90% by weight of said dextran has molecular weights less than 3,500 Daltons, and the Mw of the 10% by the weight fraction of the dextran having the highest molecular weights is below 4,500 Daltons. 2. The compound according to claim 1, wherein the content of monomer saccharide in said hydrogenated oligosaccharide is 0.5% by weight or less, based on the total weight of the hydrogenated oligosaccharide. 3. The compound according to claim 1, wherein the weight average molecular weight (Mw) is 1,600 Daltons or less and the number average molecular weight (Mn) is 1,600 Daltons or less. 4. The compound according to claim 1, wherein the apparent molecular weight (M.sub.P) of said compound is 120,000 to 180,000 Daltons, measured on an autoclaved aqueous solution prepared by dissolving in 1,000 ml water 400 g powder of hydrogenated oligosaccharide in stable solution with ferric oxyhydroxide, the amount of iron (Fe) of the powder being 25% by weight. 5. The compound according to claim 1, wherein the amount of iron (Fe) in the iron oligosaccharide compound is 50% by weight or less. 6. The compound according to claim 1, wherein the content of dimer saccharide in the hydrogenated oligosaccharide is 2.5% by weight or less, based on the total weight of the hydrogenated oligosaccharide. 7. The compound according to claim 6, wherein the content of dimer saccharide in the hydrogenated oligosaccharide is 2.3% by weight or less, based on the total weight of the hydrogenated oligosaccharide. 8. A composition comprising: a pharmacologically effective amount of the iron oligosaccharide compound according to claim 1, and at least one pharmaceutically acceptable carrier. 9. A process for preparing an iron oligosaccharide compound, comprising the steps of: (a) hydrolysing a polysaccharide so as to reduce its molecular weight, (b) hydrogenating the resulting oligosaccharide to convert functional aldehyde groups into alcohol groups, (c) fractioning the hydrogenated oligosaccharide according to molecular weight, so that the purified fraction has a weight average molecular weight between 500 and 3,000 Daltons, (d) combining the resultant fractionated hydrogenated oligosaccharide as an aqueous solution with at least one water-soluble ferric salt, (e) adding a base to the resulting aqueous solution to form ferric hydroxide, and (f) heating the resultant basic solution to transform the ferric hydroxide into ferric oxyhydroxide in association with said oligosaccharide; wherein step (c) comprises a procedure of purification by one or more membrane processes having a cut-off value between 340 and 800 Daltons, which procedure is continued until the content of dimer saccharide in the purified fraction of oligosaccharide has been reduced to 2.9% by weight or less, based on the total weight of the hydrogenated oligosaccharide, and wherein the hydrogenated oligosaccharide is hydrogenated dextran oligosaccharide having a number average molecular weight (Mn) above 500 Daltons, 90% by weight of said dextran has molecular weights less than 3,500 Daltons, and the Mw of the 10% by weight fraction of the dextran having the highest molecular weights is below 4,500 Daltons. 10. The process according to claim 9, wherein said purification is continued until the content of monomer saccharide in the purified fraction of oligosaccharide has been reduced to 0.5% by weight or less, based on the total weight of the hydrogenated oligosaccharide. 11. The process according to claim 9, wherein said dextran in step (c) is purified by one or more membrane processes having a cut-off value suitable for holding back dextran of molecular weight above 2,700 Daltons. 12. The process according to claim 9, wherein in step (e) the resulting solution is adjusted to a pH above 10 by addition of said base. 13. The process according to claim 9, wherein in step (f) heating is carried out at a temperature above 100.degree. C. until the solution turns into a black or dark brown colloidal solution, which after neutralisation is filtered through a filter, whereupon one or more stabilizers are added. 14. The process according to claim 9, wherein the resulting solution is dried to obtain a resulting iron dextran compound as a stable powder. 15. The process according to claim 14, wherein the amount of iron (Fe) in the iron dextran compound is 50% by weight or less. 16. The process according to claim 9, wherein the hydrogenation in step (b) is performed using sodium borohydride in aqueous solution. 17. The process according to claim 9, wherein stabilization following step (f) is effected by addition of at least one salt of an organic hydroxy acid. 18. The process according to claim 17, wherein the at least one salt of an organic hydroxy acid is selected from citrates. 19. A method of preventing or treating iron-deficiency anaemia, comprising; parenterally or orally administrating a pharmacologically effective amount of a therapeutical composition including the compound of claim 1 to animal or human subjects in need thereof. 20. A process for producing an injection liquid containing the compound according to claim 1, wherein the compound as a dry powder is dissolved in an aqueous medium; pH is adjusted, if necessary; optionally, stabilizer is added; and the liquid is sterilized by filtration, before it is filled into ampoules or vials, or by autoclave treatment after filling into such ampoules or vials. 21. A process for producing an injection liquid containing the compound according to claim 1, wherein a liquid containing said compound is purified, adjusted as to iron content and pH, stabilized and sterilized by filtration before being filled into ampoules or vials or by autoclave treatment after being filled into said ampoules or vials.