DRY POWDER FORMULATIONS, DOSE CONTAINERS AND INHALERS CONTAINING THE SAME, AND METHODS
Dry powder formulations (preferably configured for use with a dry powder inhaler) including a first sub-formulation that includes a first drug and a second sub-formulation that includes a second drug, the first sub-formulation and the second sub-formulation being in physical contact.
1 . A dry powder inhaler comprising:
a dose container; and
a dry powder formulation contained in the dose container, the dry powder formulation comprising:
a first sub-formulation comprising a first drug; and
a second sub-formulation comprising a second drug;
the first sub-formulation and the second sub-formulation being in physical contact within the dose container; and
the first drug being different from the second drug.
2 . The dry powder inhaler of claim 1 , wherein:
the first sub-formulation is configured as spheronized aggregates consisting of fine particles of the first drug or the first sub-formulation is configured as engineered particles consisting of the first drug, and
the second sub-formulation is configured as spheronized aggregates consisting of fine particles of the second drug or the second sub-formulation is configured as engineered particles consisting of the second drug.
3 . The dry powder inhaler of claim 1 , wherein:
the first sub-formulation is configured as spheronized aggregates consisting of fine particles of the first drug or the first sub-formulation is configured as engineered particles consisting of the first drug, and
the second sub-formulation comprises one or more excipients.
4 . The dry powder inhaler of claim 1 , wherein the first sub-formulation comprises one or more excipients and the second sub-formulation comprises one or more excipients.
5 . The dry powder inhaler of claim 1 , wherein the one or more excipients comprises a sugar, a force control agent, a phospholipid, a biocompatible polymer, or any combination thereof.
6 . The dry powder inhaler of claim 5 , wherein the sugar is present as fine excipient particles, coarse carrier particles, a force control agent, or any combination thereof.
7 . The dry powder inhaler of claim 5 , wherein the sugar comprises lactose, trehalose, sucrose, mannitol, or any combination thereof.
8 . The dry powder inhaler of claim 5 , wherein the force control agent comprises magnesium stearate.
9 . The dry powder inhaler of claim 5 , wherein the phospholipid comprises a phosphatidylcholine.
10 . The dry powder inhaler of claim 1 , wherein the first drug, the second drug, or both comprise a bronchodilator drug, anti-inflammatory drug, or both.
11 . The dry powder inhaler of claim 1 , wherein the first sub-formulation and the second sub-formulation are not intermixed or only intermixed at an interface.
12 . The dry powder inhaler of claim 1 , wherein the first sub-formulation and the second sub-formulation are fully intermixed.
13 . The dry powder inhaler of claim 1 , wherein the first sub-formulation and the second sub-formulation are partially intermixed.
14 . The dry powder inhaler of claim 1 , wherein the dose container is in the form of a capsule or a reservoir.
15 . The dry powder inhaler of claim 1 , wherein the dose container is in the form of a blister strip and the formulation is disposed within one or more blisters along the blister strip.
16 . The dry powder inhaler of claim 1 , wherein upon aerosolization
the first drug and the second drug each independently have a mass median aerodynamic diameter (MMAD) of 5 μm or less as measured according to the aerodynamic particle size distribution (APSD) Test Method.
17 . The dry powder inhaler claim 1 , wherein upon aerosolization of the dry powder formulation,
the MMAD of the first drug and the MMAD of the second drug differ by 0.5 μm or greater as measured according to the APSD Test Method.
18 . The dry powder inhaler of claim 1 , wherein upon aerosolization of the dry powder formulation,
the first drug and the second drug each independently have a fine particle fraction (FPF) of 20% or greater as measured according to the APSD Test Method.
19 . The dry powder inhaler of claim 1 , wherein upon aerosolization of the dry powder formulation,
the FPF of the first drug and the FPF of the second drug differ by 10% or greater.
20 . A method of making the dry powder inhaler of claim 1 , wherein the method comprise dispensing the formulation into the dose container.