Delivery of agents using metastable liposomes
Metastable liposomal formulations for hydrophobic drug delivery to a tissue or tissue lumen such the bladder have been developed. These are at least one micron in diameter and formed of one or more lipids having entrapped in the lipid a hydrophobic therapeutic, prophylactic or diagnostic agent. The greater stability of these liposomes, as well as the enhanced transfer of entrapped agent into the adjacent tissue, provides for better delivery, especially of hydrophobic agents such as tacrolimus which does not penetrate tissue well. The metastable liposomal formulations can be administered locally, preferably by instillation, or topically, for example, by spraying or painting, to a tissue or tissue lumen such as the bladder in need of treatment.
1. A dosage formulation of metastable liposomes comprising
(a) multilamellar metastable liposomes having a mean diameter of between one and 100 microns, inclusive,
wherein the ratio of the volume enclosed by the liposomes at 25° C. relative to the volume enclosed by the liposomes following heating to a temperature that surpasses the gel-fluid phase transition of one or more lipids forming the liposomes is greater than 1.0; and
(b) one or more hydrophobic therapeutic, prophylactic or diagnostic agent(s),
wherein the one or more hydrophobic agent(s) is entrapped within the lipid forming the liposomes,
wherein the metastable liposomes are prepared by a method comprising
(a) dispersing the lipid forming the liposomes in a co-solvent system to create an isotropic monophasic solution;
(b) mixing the isotropic monophasic solution with the hydrophobic agent to form a pre-liposomal solution;
(c) lyophilizing the pre-liposomal solution to produce a pre-liposomal lyophilized formulation; and
(d) rehydrating the pre-liposomal lyophilized formulation of step (c) to produce the liposomes.
2. The formulation of claim 1 further comprising a second therapeutic, prophylactic or diagnostic agent encapsulated within the liposomes.
3. The formulation of claim 1 in the form of a dry powder.
4. The formulation of claim 1 wherein the liposomes are suspended in a gel or solution suitable for direct administration to a tissue or tissue lumen.
5. The formulation of claim 1 wherein the hydrophobic agent is for treatment of a bladder disease or disorder.
6. The formulation of claim 5 , wherein the hydrophobic agent is tacrolimus.
7. The formulation of claim 1 wherein the liposomes comprise sphingomyelin.
8. The formulation of claim 7 wherein the liposomes have a mean diameter greater than 24.8 microns at 25° C.
9. A method for treating an individual in need thereof comprising administering to a tissue or tissue lumen a dosage formulation of metastable liposomes comprising
(a) multilamellar metastable liposomes having a mean diameter of between one and 100 microns, inclusive,
wherein the ratio of the volume enclosed by the liposomes at 25° C. relative to the volume enclosed by the liposomes following heating to a temperature that surpasses the gel-fluid phase transition of one or more lipids forming the liposomes is greater than 1.0; and
(b) one or more hydrophobic therapeutic, prophylactic or diagnostic agent(s),
wherein the one or more hydrophobic agent(s) is entrapped within the lipid forming the liposomes,
wherein the liposomes are prepared by a method comprising
(a) dispersing the lipid forming the liposomes in a co-solvent system to create an isotropic monophasic solution;
(b) mixing the isotropic monophasic solution with the hydrophobic agent to form a pre-liposomal solution;
(c) lyophilizing the pre-liposomal solution to produce a pre-liposomal lyophilized formulation; and
(d) rehydrating the pre-liposomal lyophilized formulation of step (c) to produce the liposomes.
10. The method of claim 9 wherein the liposomes further comprise a second therapeutic, prophylactic or diagnostic agent encapsulated within the liposomes.
11. The method of claim 9 wherein the formulation is in the form of a dry powder.
12. The method of claim 9 further comprising suspending the liposomes in a gel or solution suitable for direct administration to the tissue or tissue lumen.
13. The method of claim 9 , wherein the formulation is administered via a cystoscope comprising an applicator selected from the group consisting of a spray device, gauze, roller, and sponge.
14. The method of claim 9 wherein the liposomes comprise sphingomyelin.
15. The method of claim 14 wherein the liposomes have a mean diameter greater than 24.8 microns at 25° C.
16. The method of claim 9 wherein the lumen is selected from the group consisting of lumens of the respiratory tract, the gastrointestinal tract, the urogenital tract, and the reproductive tract.
17. The method of claim 9 , wherein the hydrophobic agent is tacrolimus.
18. The method of claim 9 wherein the hydrophobic agent is for treatment of a bladder disease or disorder.
19. The method of claim 18 , wherein the formulation is administered via intravesical instillation into the bladder of the individual.
20. The method of claim 19 , wherein the bladder disease or disorder is selected from the group consisting of hemorrhagic cystitis, interstitial cystitis, and cancer.
21. The formulation of claim 1 , wherein the ratio of the hydrophobic agent to the lipid forming the liposomes is between 1:1 and 0.1:1.
22. The formulation of claim 21 , wherein the hydrophobic agent occupies at least 10% by weight of the formulation.
23. The method of claim 9 , wherein the amount of the hydrophobic agent administered is between 0.1 and 50 mg, inclusive.
24. A method of making a pre-liposomal lyophilized formulation of metastable liposomes having entrapped within the lipid forming the liposomes one or more hydrophobic therapeutic, prophylactic or diagnostic agent(s), comprising:
(a) dispersing the lipid forming the liposomes in a co-solvent system to create an isotropic monophasic solution;
(b) mixing the isotropic monophasic solution with the hydrophobic agent to form a pre-liposomal solution; and
(c) lyophilizing the pre-liposomal solution to produce the pre-liposomal lyophilized formulation,
wherein the metastable liposomes are multilamellar and have a mean diameter of between one and 100 microns, inclusive, wherein the ratio of the volume enclosed by the liposomes at 25° C. relative to the volume enclosed by the liposomes following heating to a temperature that surpasses the gel-fluid phase transition of one or more lipids forming the liposomes is greater than 1.0.
25. The method of claim 24 , wherein the co-solvent system comprises tert-butyl alcohol and water.
26. The method of claim 25 , wherein the lipid is dispersed in the co-solvent system at a ratio of 2 mg lipid to 1 mL co-solvent system.
27. The method of claim 24 , further comprising the step of
(d) rehydrating the pre-liposomal lyophilized formulation of step (c) to produce a solution or suspension of the metastable liposomes.
28. The method of claim 27 , wherein the pre-liposomal lyophilized formulation is rehydrated with a sterile liquid selected from the group consisting of water, saline, phosphate buffered saline, polyvinyl pyrrolidone solution, alginate solution, and hyaluronic acid solution.
29. A pre-liposomal lyophilized formulation comprising one or more lipids and at least one hydrophobic therapeutic, prophylactic, or diagnostic agent which is prepared by a method comprising
(a) dispersing lipid(s) in a co-solvent system to create an isotropic monophasic solution;
(b) mixing the isotropic monophasic solution with the at least one hydrophobic agent to form a pre-liposomal solution; and
(c) lyophilizing the pre-liposomal solution to produce a pre-liposomal lyophilized formulation;
wherein the pre-liposomal lyophilized formulation, after rehydration, produces multilamellar metastable liposomes having a mean diameter of between one and 100 microns, inclusive,
wherein the ratio of the volume enclosed by the liposomes at 25° C. relative to the volume enclosed by the liposomes following heating to a temperature that surpasses the gel-fluid transition of the one or more lipids forming the liposome is greater than 1.0, and
wherein the at least one hydrophobic agent is entrapped within the liposome.