Method of treating pancreatic cancer
US-2024415804-A1 · Dec 19, 2024 · US
US9579303B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9579303-B2 |
| Application number | US-88443306-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 14, 2006 |
| Priority date | Feb 15, 2005 |
| Publication date | Feb 28, 2017 |
| Grant date | Feb 28, 2017 |
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The disclosure relates to compositions, preferably in the form of a powder and/or granules, which contain as principal components a first component selected from the group consisting of isoflavones, soy products containing at least one isoflavone, and mixtures thereof, together with a polysaccharide as second component. A preferred first component is genistein or a pharmaceutically acceptable salt or derivative thereof (e.g. genistin). A preferred second component is pectin. The disclosure further relates to a process for the manufacture of such compositions, and their use in dietary supplements, pharmaceutical and personal care compositions. The disclosure is also directed to the use of a polysaccharide for improving the flowability of a component selected from the group consisting of isoflavones, soy products, preferably those containing at least one isoflavone, and mixtures thereof.
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The invention claimed is: 1. A method of improving the flowability of a powder consisting of isoflavone; said method consisting of introducing water-soluble pectin into the powder. 2. The method according to claim 1 wherein the isoflavone is an isoflavone of formula I, a pharmaceutically acceptable salt or a glycoside thereof, wherein formula I is: wherein R signifies hydrogen, C 1-18 -alkyl or C 1-18 alkylcarbonyl, R 1 signifies hydrogen or hydroxyl or C 1-18 -alkyloxy or C 1-18 -alkylcarbonyloxy, and R 2 signifies hydroxyl or C 1-18 -alkoxy or C 1-18 -alkylcarbonyloxy. 3. The method according to claim 2 , wherein R is hydrogen and R 1 and R 2 are both hydroxyl. 4. The method of claim 1 , wherein the water-soluble pectin is introduced in the form of a slurry. 5. The method of claim 4 , wherein the slurry is an aqueous slurry. 6. A composition consisting of a powder or a plurality of granules, said powder or plurality of granules consisting of: a) a first component which is isoflavone in a quantity of 95-99.9 weight %; and b) a second component which is pectin in a quantity of 0.1-5 weight-%. 7. The composition of claim 6 , wherein the isoflavone in the powder, or in the plurality of granules, is coated or partially coated with the pectin. 8. The composition according to claim 6 , wherein the isoflavone is selected from the group consisting of isoflavones of formula I, pharmaceutically acceptable salts or glycosides thereof wherein formula I is: wherein R signifies hydrogen, C 1-18 -alkyl or C 1-18 alkylcarbonyl, R 1 signifies hydrogen or hydroxyl or C 1-18 -alkyloxy or C 1-18 -alkylcarbonyloxy, and R 2 signifies hydroxyl or C 1-18 -alkoxy or C 1-18 -alkylcarbonyloxy. 9. The composition of claim 8 , wherein the isoflavone in the powder, or in the plurality of granules, is coated or partially coated with the pectin. 10. The composition according to claim 8 , wherein R is hydrogen and R 1 and R 2 are both hydroxyl. 11. The composition of claim 10 , wherein the isoflavone in the powder, or in the plurality of granules, is coated or partially coated with the pectin. 12. The composition of claim 6 in a dosage form selected from the group consisting of a tablet, and capsule. 13. The dosage form according to claim 12 , wherein the dosage form is a tablet. 14. A dietary, pharmaceutical and personal care composition comprising a composition as claimed in claim 6 . 15. A process for the manufacture of a composition according to claim 6 , which comprises preparing a slurry of the-components having a solid content of 10 to 70% by weight, based on the total weight of the slurry, and spray-drying the slurry. 16. The process of claim 15 , wherein the slurry has a solid content of 25 to 50% by weight. 17. A process for the manufacture of a composition according to claim 6 , which comprises forming a fluidized bed of the first component with or without pectin within a fluidized-bed drying device fitted with spray means, said fluidized bed being fluidized by air or an inert gas, and spraying a solution, of a pectin or only water in the form of an atomized mist onto the fluidized particles until the composition is obtained. 18. The process according to claim 15 or 17 , wherein the first component is an isoflavone of the formula I, wherein R signifies hydrogen, C 1-18 -alkyl or C 1-18 alkylcarbonyl, R 1 signifies hydrogen or hydroxyl or C 1-18 -alkyloxy or C 1-18 -alkylcarbonyloxy, and R 2 signifies hydroxyl or C 1-18 -alkoxy or C 1-18 -alkylcarbonyloxy, or a pharmaceutically acceptable salt or glycoside thereof. 19. The process according to claim 18 , wherein R is hydrogen and R 1 and R 2 are both hydroxyl. 20. A process for the manufacture of a composition according to claim 6 , which comprises forming a fluidized bed of the first component within a fluidized-bed drying device fitted with spray means, said fluidized bed being fluidized by air or an inert gas, and spraying an aqueous solution of a pectin and water in the form of an atomized mist onto the fluidized particles until the composition is obtained.
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