DPI formulation containing sulfoalkyl ether cyclodextrin
An inhalable dry powder formulation containing SAE-CD and an active agent is provided. The formulation is adapted for administration by DPI. The SAE-CD serves as a carrier rather than as an absorption enhancer. The average particle size of the SAE-CD is large enough to preclude (for the most part) pulmonary deposition thereof. Following release from the DPI device, the SAE-CD-containing particles dissociate from the active agent-containing particles in the buccal cavity or throat, after which the active agent-containing particles continue deeper into the respiratory tract. The physicochemical and morphological properties of the SAE-CD are easily modified to permit optimization of active agent and carrier interactions. Drugs having a positive, neutral or negative electrostatic charge can be delivered by DPI when SAE-CD is used as a carrier.
1. A pharmaceutical composition comprising an active agent; and
a sulfoalkyl ether cyclodextrin composition comprising agglomerated particles comprising sulfoalkyl ether cyclodextrin, wherein the agglomerated particles are made by spray agglomeration wherein the sulfoalkyl cyclodextrin composition has a micro-flow fractal dimension analysis of about 1.0-1.2, wherein the sulfoalkyl ether cyclodextrin composition comprises less than 10% by weight moisture and has a property selected from the group consisting of a bulk density of 0.34 g/cc to 0.55 g/cc, a CARR's index of about 10% to about 40%, and a median particle diameter of about 10 microns to about 300 microns, or a combination thereof, and wherein the agglomerated particles have a rough surface.
2. A pharmaceutical dosage form comprising the pharmaceutical composition of claim 1 .
3. The pharmaceutical dosage form of claim 2 , wherein the dosage form is a powder.
4. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition has a bulk density of 0.34 g/cc to 0.55 g/cc.
5. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises a CARR's index of about 10% to about 40%.
6. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises particles with a median particle diameter of about 10 microns to about 300 microns.
7. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin is a compound, or a mixture of compounds, of the Formula 1:
wherein:
n is 4, 5, or 6;
R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are each, independently, O − or a O—(C 2-6 alkylene)-SO 3 − group, wherein at least one of R 1 to R 9 is independently a O—(C 2 -C 6 alkylene)-SO 3 − group; and
S 1 , S 2 , S 3 , S 4 , S 5 , S 6 , S 7 , S 8 , and S 9 , are each, independently, a pharmaceutically acceptable cation.
8. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises particles with a median particle diameter of about 175 microns to about 277 microns.
9. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises particles with a median particle diameter of about 37 microns to about 125 microns.
10. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises a particle size distribution span of about 1.5 to about 2.9.
11. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises a moisture content of less than 8% by weight.
12. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises a moisture content of less than 2.5% by weight.
13. The pharmaceutical composition of claim 1 , wherein the sulfoalkyl ether cyclodextrin composition comprises a moisture content of less than 1% by weight.
14. The pharmaceutical composition of claim 1 , further comprising an excipient selected from the group consisting of an antioxidant, acidifying agent, alkalizing agent, buffering agent, solubility-enhancing agent, penetration enhancer, electrolyte, fragrance, glucose, glidant, stabilizer, bulking agent, cryoprotectant, plasticizer, flavor, sweetener, surface tension modifier, density modifier, volatility modifier, hydrophilic polymer, water soluble polymer, and combinations thereof.
15. The pharmaceutical composition of claim 1 , wherein the composition is formulated for administration by inhalation.
16. The pharmaceutical composition of claim 7 , wherein n is 5.