Sustained release of antiinfectives
View Patent ↗Provided, among other things, is a method of treating or ameliorating pulmonary infection in a cystic fibrosis patient comprising pulmonary administration of an effective amount of a liposomal/complexed antiinfective to the patient, wherein the (i) administrated amount is 50% or less of the comparative free drug amount, or (ii) the dosing is once a day or less, or (iii) both.
1. A method of treating a Pseudomonas aeruginosa infection in the lungs of a patient in need thereof, comprising administering to the lungs of the patient an effective amount of a liposomal amikacin formulation, which comprises amikacin and a lipid component, wherein said lipid component consists essentially of a sterol and a phosphatidylcholine, and the lipid and amikacin have a ratio of less than 2.5:1 by weight.
2. The method of claim 1 , wherein the patient is a cystic fibrosis patient.
3. The method of claim 1 , wherein the phosphatidylcholine is selected from the group consisting of egg phosphatidylcholine (EPC), soy phosphatidylcholine (SPC), hydrogenated egg phosphatidylcholine (HEPC), hydrogenated soy phosphatidylcholine (HSPC), dipalmitoyl phosphatidylcholine (DPPC), dioleoyl phosphatidylcholine (DOPC), dimyristoyl phosphatidylcholine (DMPC), distearoyl phosphatidylcholine (DSPC), palmitoylstearoyl phosphatidylcholine (PSPC), and mixtures thereof.
4. The method of claim 3 , wherein the phosphatidylcholine is DPPC.
5. The method of claim 1 , wherein the sterol is cholesterol.
6. The method of claim 1 , wherein the sterol is cholesterol and the phosphatidylcholine is DPPC.
7. The method of claim 6 , wherein the DPPC and cholesterol have a mole ratio of about 19:1, 9:1, 4:1, 13:7or 1:1.
8. The method of claim 7 , wherein the DPPC and cholesterol have a mole ratio of about 1:1.
9. The method of claim 1 , wherein the administration has a dosing frequency ranging from once a day to once a week during a 14-day treatment period.
10. The method of claim 9 wherein the administration has a dosing frequency of once a day.
11. The method of claim 9 wherein the administration has a dosing frequency of once every two days.
12. The method of claim 9 , wherein the administration has a dosing frequency of once every three days.
13. The method of claim 9 , wherein the administration has a dosing frequency of once a week.
14. The method of claim 1 , wherein the lipid to amikacin ratio is less than 1.1:1 by weight.
15. The method of claim 1 , wherein the amikacin is provided as amikacin sulfate.
16. The method of claim 15 , wherein the phosphatidylcholine is DPPC.
17. The method of claim 15 , wherein the sterol is cholesterol.
18. The method of claim 15 , wherein the sterol is cholesterol and the phosphatidylcholine is DPPC.
19. The method of claim 18 , wherein the DPPC and cholesterol have a mole ratio of about 19:1, 9:1, 4:1, 13:7or 1:1.
20. The method of claim 18 , wherein the DPPC and cholesterol have a mole ratio of about 1.0:1.
21. The method of claim 18 , wherein the lipid and amikacin have a ratio of less than 1.1:1 by weight.
22. The method of claim 18 , wherein the patient is a cystic fibrosis patient.
23. The method of claim 6 , wherein the DPPC and cholesterol have a mole ratio ranging from 19:1 to 1:1.
24. The method of claim 18 , wherein the DPPC and cholesterol have a mole ratio ranging from 19:1 to 1:1.
25. A method of treating a Pseudomonas aeruginosa infection in the lungs of a patient in need thereof, comprising administering to the lungs of a patient in need thereof an effective amount of a liposomal amikacin formulation, which comprises amikacin and a lipid component, wherein said lipid component consists essentially of cholesterol and dipalmitoylphosphatidylcholine, the lipid and amikacin have a ratio of less than 1.1:1 by weight, and the amikacin is provided as amikacin sulfate.
26. The method of claim 25 , wherein the patient is a cystic fibrosis patient.