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|Abstract:||Controlled release preparation containing a number of beads comprising a salt of metoprolo as the main soluble component, a method for the production thereof and the use in the treatment of cardiovascular disorders.|
|Inventor(s):||Jonsson; Ulf E. (Molndal, SE), Sandberg; John A. (Molndal, SE), Sjogren; John A. (Molnycke, SE)|
|Assignee:||Aktiebolaget Hassle (Molndal, SE)|
1. Controlled release preparation comprising a plurality of beads having a soluble component comprising at least 95% weight/weight of a salt of metoprolol which has a solubility of less
than 600 mg/ml in water at 25.degree. C. and a metoprolol permeable polymeric membrane coating surrounding each of said beads, said coating consisting essentially of ethylcellulose or a mixture of ethylcellulose and hydroxypropylmethylcellulose wherein
the coating is present in amounts such that the metoprolol is released through the coating over a period of at least 15 hours virtually independent of pH in the interval pH 1-8.
2. Preparation according to claim 1 wherein the size of the beads is in the range of 0.25-2 mm.
3. Preparation according to claim 2 wherein the size of the beads is in the range of 0.35-1.0 mm.
4. Preparation according to claim 1 wherein at least 50% of the dose of metoprolol is released at a rate of 3-7 w/w %/hour.
5. Preparation according to claim 1 wherein the salt of metoprolol has a solubility of 30-600 mg/ml.
6. Preparation according to claim 5 wherein the salt of metoprolol is formed of an organic carboxylic acid.
7. Preparation according to claim 6 wherein the salt of metoprolol is the succinate or fumarate of racemic metoprolol.
8. Preparation according to claim 6 wherein the salt of metoprolol is the bensoate or sorbate of the S-enantiomer of metoprolol.
9. Preparation according to claim 1 wherein the beads comprise at least 95 w/w % of metoprolol.
10. Preparation according to claim 1 wherein the beads further comprise an insoluble core disposed in the interior of the soluble component.
11. Preparation according to claim 10 wherein the insoluble cores have a size of 0.1-1.0 mm.
12. Preparation according to claim 10 wherein the insoluble cores have a size of 0.15-0.3 mm and are covered with a layer of the soluble component to give beads having a size of 0.35-1.0 mm.
13. Preparation according to claim 9 wherein the beads have a size of 0.35-1.0 mm.
14. Preparation according to claim 1 wherein polymeric membrane contains ethyl cellulose together with hydroxypropylmethyl cellulose.
15. A pharmaceutical preparation containing the controlled release preparation according to claim 1 filled into hard gelatine capsules.
16. A pharmaceutical preparation comprising the controlled release preparation according to claim 1 and pharmaceutical additives compressed to tablets which disintegrate to release the preparation when the tablets are brought into contact with gastro-intestinal fluids.
17. Method of producing a preparation according to claim 1 comprising spray coating beads comprising a salt of metoprolol with a membrane-forming solution consisting essentially of ethylcellulose.
18. A method for the treatment of cardiovascular disorders comprising administering a composition according to claim 1 to a host in need of such treatment in a therapeutically effective amount.
19. Preparation according to claim 10, wherein the insoluble cores have a size of 0.15-0.3 mm.
20. Preparation according to claim 1, wherein the amount of coating is such that at least 75% of the metoprolol is released over a period of 20 hours.
21. Preparation according to claim 1, wherein the soluble component comprises at least 95% w/w of the salt of metoprolol.
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