Pulmonary delivery of a fluoroquinolone
A composition for pulmonary administration comprises a fluoroquinolone betaine, such as ciprofloxacin betaine, and an excipient. In one version, the particles have a mass median aerodynamic diameter from about 1 μm to about 5 μm, and the fluoroquinolone has a half life in the lungs of at least 1.5 hours. The composition is useful in treating an endobronchial infection, such as Pseudomonas aeruginosa , and is particularly useful in treating cystic fibrosis.
1. A powder composition for pulmonary administration in a unit dose receptacle, the powder composition comprising:
particles comprising a ciprofloxacin betaine hydrate and an excipient, wherein the particles have a mass median aerodynamic diameter from about 1 μm to about 5 μm and wherein the ciprofloxacin has a half life in the lungs of at least 1.5 hours, and wherein the composition has a rugosity of from about 3 to 10 and wherein the mass of the composition in the unit dose receptacle is sufficient to provide at least about a 10 mg dose to the lungs of a human patient in three inhalations or less.
2. A composition according to claim 1 wherein the ciprofloxacin betaine hydrate is in crystalline form.
3. A composition according to claim 1 wherein the ciprofloxacin betaine hydrate is ciprofloxacin betaine 3.5 hydrate.
4. A composition according to claim 1 wherein the composition provides an emitted dose in a passive dry powder inhaler of at least about 50%.
5. A composition according to claim 1 in a unit dose receptacle wherein the mass of the composition in the unit dose receptacle is sufficient to provide at least about a 16 mg dose to the lungs in three inhalations or less.
6. A composition according to claim 1 wherein the composition in the unit dose receptacle comprises at least about 16 mg of ciprofloxacin betaine hydrate.
7. A composition according to claim 1 wherein the excipient comprises a phospholipid, a metal ion or both.
8. A composition according to claim 5 wherein the receptacle contains a therapeutic dose of the composition for treating cystic fibrosis.
9. A composition according to claim 1 wherein the particles have a bulk density of less than 0.6 g/cm 3 .
10. A composition according to claim 1 wherein the composition comprises from 50% to 70% ciprofloxacin betaine hydrate, from 15% to 35% phospholipid, and from 1% to 3% metal ion containing material.
11. A composition according to claim 1 wherein the unit dose receptacle comprises a capsule.
12. A composition according to claim 11 wherein the capsule comprises hydroxypropylmethylcellulose (HPMC).
13. A composition according to claim 1 in combination with a dry powder aerosolization apparatus.
14. A composition and apparatus according to claim 13 wherein the dry powder aerosolization apparatus is adapted to aerosolize the composition within the apparatus by the flow of air through the apparatus.
15. A composition and apparatus according to claim 14 wherein the flow of air is caused by the patient's inhalation.
16. A composition according to claim 1 wherein the mass of the composition in the unit dose receptacle is sufficient to provide at least about a 10 mg dose to the lungs in a single inhalation.
17. A powder composition for pulmonary administration, the powder composition comprising:
particles comprising ciprofloxacin betaine 3.5 hydrate and an excipient, wherein the composition comprises from 50% to 70% ciprofloxacin betaine 3.5 hydrate;
wherein the particles have a mass median aerodynamic diameter from about 1 μm to about 5 μm and wherein the ciprofloxacin has a half life in the lungs of at least 1.5 hours, and
wherein the composition has a rugosity of from about 3 to 10.
18. A composition according to claim 17 wherein the composition provides an emitted dose in a passive dry powder inhaler of at least about 50%.
19. A composition according to claim 17 in a unit dose receptacle wherein the mass of the composition in the unit dose receptacle is sufficient to provide at least about a 10 mg dose to the lungs.
20. A composition according to claim 17 wherein the excipient comprises a phospholipid, a metal ion or both.
21. A composition according to claim 17 wherein the particles have a bulk density of less than 0.6 g/cm 3 .
22. A composition according to claim 17 wherein the composition comprises from 15% to 35% phospholipid, and from 1% to 3% metal ion containing material.