IP Library Patent Application 14934377
Patent Application
App. No. 14/934,377

Dry Powder For Inhalation

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Quick Facts
Patent No.
US None
App. No.
14/934,377
Abstract

The present invention provides dry powder formulations for inhalation having improved moisture resistance such that the powders maintain a high fine particle dosage or fine particle fraction following storage under relatively extreme temperature and humidity conditions.

Claims (25)

1 - 13 . (canceled)

14 . A dry powder inhaler, comprising

a) a pre-dosed unit containing a dry powder formulation comprising:

i) a pharmaceutically inactive carrier having particles of noninhalable particle size,

ii) a pharmaceutically active component comprising at least one finely divided pharmaceutically active compound having particles of inhalable particle size, and

iii) magnesium stearate as a pulverulent material present in an amount of 0.5 to 5% by weight, based on the total weight of the formulation; and

b) means for delivering doses of the pharmaceutically active compound for inhalation.

15 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active compound is a hygroscopic compound capable of absorbing at least 0.5% by weight of its own weight of absorptively bound water when stored in air having a relative humidity of 50%.

16 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active compound is a hydrophilic compound having a wetting angle of less than 90°.

17 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active compound is a hydrophilic compound having a wetting angle of less than 70°.

18 . The dry powder inhaler of claim 14 , wherein the magnesium stearate is present in an amount of 0.5% to 0.75% by weight, based on the total weight of the formulation.

19 . The dry powder inhaler of claim 14 , wherein the carrier is selected from the group consisting of monosaccharides, disaccharides, sugar alcohols, polylactic acid and cyclodextrin.

20 . The dry powder inhaler of claim 14 , wherein the carrier is selected from the group consisting of glucose, lactose monohydrate and trehalose.

21 . The dry powder inhaler of claim 14 , wherein the formulation further comprises particles of micronized lactose monohydrate wherein at least 50% of the particles thereof have a maximum particle size of 10 um.

22 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active compound is formoterol or a pharmaceutically acceptable salt thereof.

23 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active compound is selected from the group consisting of formoterol fumarate, formoterol tartrate, ipratropium bromide and tiotropium bromide.

24 . The dry powder inhaler of claim 14 , wherein the formulation further comprises a second pharmaceutically active compound having particles of inhalable size.

25 . The dry powder inhaler of claim 14 , wherein the pharmaceutically active component comprises a) a member selected from the group consisting of formoterol fumarate, formoterol tartrate, levalbuterol sulfate and salmeterol xinafoate, and b) a corticosteroid.

26 . (canceled)

27 . (canceled)

28 . The dry powder inhaler of claim 14 , wherein said predosed unit is in the form of a capsule or blister pack.

29 . The inhaler of claim 14 , wherein said dry powder formulation of a) comprises a fine particle fraction (FPF), said formulation exhibiting a reduction in said FPF by less than 50% within 10 days of storage at 40° C. and 75% relative atmospheric humidity.

30 . The inhaler of claim 14 , wherein the pharmaceutically active component does not comprise salbutamol sulfate, salmeterol xinafoate, or beclomethasone dipropionate.

31 . The inhaler of claim 14 , wherein the pharmaceutically active compound is fluticasone.

32 . The inhaler of claim 14 , wherein the pharmaceutically active compound is tiotropium, ipratropium, oxitropium or glycopyrronium.