Capsules for dry powder inhalers and methods of making and using same

• US 20040025876A1
• Filed: 05/07/2003
• Published: 02/12/2004
• Est. Priority Date: 05/07/2002
• Status: Abandoned Application

• Current Assignee: Novartis Pharma AG (Novartis Ag)
• Original Assignee: Novartis Pharma AG (Novartis Ag)
• Inventors: Miller, Danforth, Ballesteros, David Lechuga
• Application Number:
  US10/430,832
• Publication Number:
  US 20040025876A1
• Time in Patent Office: Days
• US Class Current: 128/203.15
• CPC Class Codes: A61K 9/0075 for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
• CPC Class Codes: A61K 9/4816 Wall or shell material
• CPC Class Codes: A61P 11/00 Drugs for disorders of the respiratory system
• CPC Class Codes: A61P 31/04 Antibacterial agents

Abstract

Pulmonary delivery of dry powder formulations by aerosol inhalation has received much attention as an attractive alternative to intravenous, intramuscular, and subcutaneous injection, since this approach eliminates the necessity for injection syringes and needles. The present invention provides dry powder filled cellulose-based capsules having particular utility for use with dry powder inhalers. Such capsules not only readily coordinate with conventional DPIs but also coordinate with conventional powder filling technologies, thereby saving time, labor and cost. The invention further provides a novel procedure for determining, ab initio, appropriate and optimal conditions for preparing such powder filled capsules. Specifically, when packaging dry powder formulations for long-term storage, it is important to ensure that the water content of the powder does not exceed the critical moisture point, that point at which the powder loses physical and chemical stability. The present invention describes means for predicting equilibrium moisture contents, which in turn can be used to establish suitable capsule preparation and filling protocols.

Claims

1. A unit dose package comprising:

(a) a dry powder formulation having a maximum critical moisture point and (b) a capsule receiving said dry powder formulation therein and having an initial moisture content such that the moisture content of the powder does not exceed its maximum critical moisture point when the powder is in equilibrium with the capsule, wherein the formulation is storage stable within said capsule at room temperature.

2. The unit dose package of claim 1, wherein the capsule material comprises a cellulose derivative.

3. The unit dose package of claim 2 wherein the cellulose derivative is hydroxypropyl methyl cellulose (HPMC).

4. The unit dose package of claim 1, wherein the dry powder formulation comprises a phospholipid.

5. The unit dose package of claim 4 wherein the dry powder formulation comprises a bulk density of less than 1.0 g/cm³.

6. The unit dose package of claim 4 wherein the dry powder formulation comprises a bulk density of less than 0.3 g/cm³.

7. The unit dose package of claim 4 wherein the dry powder formulation comprises a bulk density of less than 0.1 g/cm³.

8. The unit dose package of claim 4, wherein the dry powder formulation includes a pharmaceutically active agent.

9. The unit dose package of claim 5, wherein the pharmaceutically active agent is selected from the group consisting of sumatriptan, frovatriptan, rizatriptan, zolmatriptan, alprazolam, midazolam, ciprofloxacin, amphotericin B, tobramycin, LHRH, leuprolide, insulin, nicotine and teriparatide.

10. The unit dose package of claim 8 wherein the dry powder formulation further comprises a minimum critical moisture point.

11. The unit dose package of claim 1 wherein the ratio of the mass of the capsule (dry basis) :

mass of dry powder formulation is less than 8.0.

12. The unit dose package of claim 1 wherein the ratio of the mass of the capsule (dry basis) :

mass of dry powder formulation is less than 2.5.

13. The unit dose package of claim 1 wherein the ratio of the mass of the capsule (dry basis):

mass of dry powder formulation is less than 0.8.

14. The unit dose package of claim 8 wherein the package is stored within a sealed environment.

15. The unit dose package of claim 14 wherein a dessicant is stored within the sealed environment.

16. The unit dose package of claim 8 wherein the maximum critical moisture point is less than about 4 wt %.

17. The unit dose package of claim 8 wherein the maximum critical moisture point is less than about 3 wt %.

18. The unit dose package of claim 8 wherein the capsule contains 1 mg-100 mg of said formulation.

19. The unit dose package of claim 8 wherein the capsule contains 5 mg-75 mg of said formulation.

20. The unit dose package of claim 1 wherein the powder is a respirable dry powder formulation.

25. A dry powder inhaler assembly comprising:

the unit dose package according to claim 1;

an actuable perforating element adapted to access the contents of the capsule of said unit dose package to release the dry powder formulation received therein; and

a mouthpiece in fluid communication with the contents of the capsule through which the released dry powder formulation is inspired into a patient'"'"'s lungs.

26. The dry powder assembly of claim 25, wherein said perforating element is handactuated.

27. The dry powder assembly of claim 25, wherein said perforating element is actuated by a rotational twisting motion.

28. The dry powder assembly of claim 25, wherein said perforating element is actuated by a horizontal sliding motion.

29. The dry powder assembly of claim 25, wherein said perforating element is actuated by the interconnection of mating screw threads.

21. A method of preparing a capsule adapted to contain a dry powder formulation comprising the steps of:

pre-equilibrating the capsule below a maximum relative humidity; and

filling the capsule with the dry powder formulation at a relative humidity pre-selected such that when in equilibrium with the capsule, the moisture content of the powder does not exceed its maximum critical moisture point, thereby ensuring the storage stability of the powder in the capsule.

22. The method of claim 21, wherein the capsule is pre-equilibrated at a relative humidity below 30%.

23. The method of claim 21, wherein the capsule is pre-equilibrated at an RH below 20%.

24. The method of claim 21 wherein the maximum relative humidity is predetermined from the mass and moisture sorption isotherm of the capsule and those of the powder formulation.