Capsules containing high doses of levodopa for pulmonary use
View Patent ↗The present invention provides a capsule containing an inhalable powder composition wherein the composition comprises about 75% by weight or more levodopa, dipalmitoylphosphatidylcholine (DPPC) and a salt characterized by a working density of less than about 100 g/L. The invention further provides a capsule containing an inhalable powder composition wherein the composition comprises about 75% by weight or more levodopa, dipalmitoylphosphatidylcholine (DPPC) and a salt characterized by a working density of less than about 100 g/L wherein the capsule material comprises hydroxypropylmethylcellulose (HPMC) and titanium dioxide.
1. A capsule for use in an inhalation device filled with a dry powder comprising levodopa and having a working density of between about 0.02 to about 0.1 g/cm 3 , and containing a capsule shell comprising hydroxypropyl methylcellulose (HPMC) and titanium dioxide;
wherein said capsule emits more powder comprising levodopa upon actuation of the inhalation device as compared to a capsule that comprises HPMC and is free of titanium dioxide; and
wherein said dry powder comprises about 75% by weight or more of levodopa.
2. The capsule of claim 1 , wherein said working density is between about 0.02 g/cm 3 to about 0.05 g/cm 3 .
3. The capsule of claim 1 , wherein said dry powder comprises from about 2 to about 8% of water by weight.
4. The capsule of claim 3 , wherein said dry powder comprises from about 5 to about 6% of water by weight.
5. The capsule of claim 1 , wherein said capsule is a 00 size capsule.
6. The capsule of claim 5 , wherein said dry powder comprises between about 15 and 50 milligrams of levodopa.
7. The capsule of claim 6 , wherein said dry powder comprises between about 25 and 35 milligrams of levodopa.
8. The capsule of claim 1 , wherein said dry powder further comprises a salt.
9. The capsule of claim 8 , wherein said salt is sodium chloride.
10. The capsule of claim 8 , wherein said dry powder further comprises a phospholipid.
11. The capsule of claim 10 , wherein said phospholipid is dipalmitoylphosphatidylcholine (DPPC).
12. The capsule of claim 1 wherein the dry powder further comprises DPPC and sodium chloride.
13. The capsule of claim 1 wherein said dry powder comprises a fine particle fraction (FPF) between about 50 to about 70% of the nominal dose.
14. The capsule of claim 1 wherein the capsule is filled with about 30 to about 50 milligrams of dry powder.