Stabilized tolterodine tartrate formulations
View Patent ↗A method of making a pharmaceutical composition containing tolterodine L-tartrate stabilized against degradation with an acid. Acid-stabilized tolterodine L-tartrate may be used as an active ingredient in various types of immediate release and controlled release dosage forms, including tablets, capsules, and beads.
1. A method of making a drug-containing bead, said method comprising the steps of:
combining tolterodine-L-tartrate with a stabilizing amount of a pharmaceutically acceptable non-polymeric pH-modifying acid having a pK a of less than 5.0 to obtain an acid-stabilized tolterodine-L-tartrate composition which does not contain oxybutynin;
depositing a seal layer on an inert core, said seal layer being formed from a non-polymeric hydrophobic material; and
depositing a layer containing said acid-stabilized tolterodine-L-tartrate on said seal layer.
2. The method of claim 1 , wherein the pH-modifying acid is a non-polymeric acid having at least a first pK a of less than 5.0.
3. The method of claim 1 , wherein the pH-modifying acid is selected from the group consisting of acetic acid, benzoic acid, fumaric acid, lactic acid, malic acid, propionic acid, hydrochloric acid, phosphoric acid, sulfuric acid, tartaric acid, citric acid, ascorbic acid, stereoisomers thereof, and mixtures thereof.
4. The method of claim 1 , wherein said layer containing said acid-stabilized tolterodine-L-tartrate is an immediate release layer.
5. The method of claim 4 , wherein said immediate release layer further comprises a water-soluble or water-swellable polymer.
6. The method of claim 1 , further comprising a step of depositing a layer containing a controlled-release polymer on said layer containing said acid-stabilized tolterodine-L-tartrate.
7. A method of making a solid pharmaceutical composition, said method comprising the steps of:
combining tolterodine-L-tartrate in solid form with a stabilizing amount of a pharmaceutically acceptable non-polymeric pH-modifying acid having a pK a of less than 5.0 to obtain a solid acid-stabilized tolterodine-L-tartrate composition which does not contain oxybutynin; and
combining said solid acid-stabilized tolterodine-L-tartrate composition with at least one pharmaceutically acceptable excipient to form a solid acid-stabilized mixture.
8. The method of claim 7 , wherein the pH-modifying acid is selected from the group consisting of acetic acid, benzoic acid, fumaric acid, lactic acid, malic acid, propionic acid, hydrochloric acid, phosphoric acid, sulfuric acid, tartaric acid, citric acid, ascorbic acid, stereoisomers thereof, and mixtures thereof.
9. The method of claim 7 , wherein said pharmaceutical composition is a tablet;
said method further comprising the step of compressing said acid-stabilized mixture to form said tablet.
10. The method of claim 9 , wherein said at least one pharmaceutically acceptable excipient comprises microcrystalline cellulose, hydroxypropylmethylcellulose, sodium starch glycolate, starch, xylitol, fructose, sorbitol, calcium phosphate, calcium sulfate, calcium carbonate, dextrose, lactose, polyvinylpyrrolidone, crosslinked polyvinylpyrrolidone, or a mixture thereof.
11. The method of claim 9 , further comprising a step of coating said tablet with a polymer.
12. The method of claim 11 , wherein said polymer is hydroxypropylmethylcellulose.
13. The method of claim 11 , wherein said polymer is ethylcellulose.
14. The method of claim 7 , wherein said pharmaceutical composition is a capsule;
said method further comprising the step of filling said acid-stabilized mixture into a capsule shell.
15. The method of claim 14 , wherein said at least one pharmaceutically acceptable excipient comprises microcrystalline cellulose, hydroxypropylmethylcellulose, sodium starch glycolate, starch, xylitol, fructose, sorbitol, calcium phosphate, calcium sulfate, calcium carbonate, dextrose, lactose, polyvinylpyrrolidone, crosslinked polyvinylpyrrolidone, or a mixture thereof.
16. The method of claim 15 , further comprising a step of coating said capsule with a polymer.
17. The method of claim 16 , wherein said polymer is hydroxypropylmethylcellulose.
18. The method of claim 16 , wherein said polymer is ethylcellulose.
19. The method of claim 7 , wherein said pharmaceutical composition is a drug-containing bead;
said method further comprising the steps of:
depositing a seal layer on an inert core, said seal layer being formed from a non-polymeric hydrophobic material; and
depositing a layer containing said acid-stabilized mixture on said seal layer.
20. The method of claim 19 , wherein said at least one pharmaceutically acceptable excipient is a water-swellable or water-soluble polymeric binder.