Use of simple amino acids to form porous particles
View Patent ↗Particles having a tap density of less than 0.4 g/cm 3 include a hydrophobic amino acid or salt thereof and a therapeutic, prophylactic or diagnostic agent or any combination thereof. Preferred particles include a phospholipid, have a median geometric diameter between about 5 and about 30 microns and an aerodynamic diameter between about 1 and about 5 microns. The particles can be formed by spray-drying and are useful for delivery to the pulmonary system.
1. A method of preparing particles having a tap density less than 0.4 g/cm 3 comprising:
(a) forming a mixture including a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and an amino acid or a salt thereof; and
(b) spray-drying said mixture to produce particles having a tap density less than about 0.4 g/cm 3 .
2. The method of claim 1 , wherein the particles have a median geometric diameter of between about 5 micrometers and about 30 micrometers.
3. The method of claim 1 , wherein the particles have an aerodynamic diameter of between about 1 and about 5 microns.
4. The method of claim 3 , wherein the particles have an aerodynamic diameter of between about 1 and about 3 microns.
5. The method of claim 3 , wherein the particles have an aerodynamic diameter of between about 3 and 5 microns.
6. The method of claim 1 , wherein the amino acid is hydrophobic.
7. The method of claim 6 , wherein the hydrophobic amino acid is selected form the group consisting of leucine, isoleucine, alanine, valine, phenylalanine and any combination thereof.
8. The method of claim 3 , wherein the hydrophobic amino acid is present in the particles in an amount of at least 10% weight.
9. The method of claim 1 , wherein the therapeutic, prophylactic or diagnostic agent is present in the particles in an amount ranging from about 1 to about 90% weight.
10. The method of claim 1 , wherein the particles further comprise a surfactant.
11. The method of claim 1 , wherein the particles further comprise a phospholipid.
12. The method of claim 11 , wherein the phospholipid is endogenous to the lung.
13. The method of claim 11 , wherein the phospholipid is selected from the group consisting of phosphatidylcholines, phosphatidylethanolamines, phosphatidylglycerols, phosphatidylserines, phosphatidylinositols and combinations thereof.
14. The method of claim 1 , wherein the mixture comprises an organic solvent.
15. The method of claim 1 , wherein the mixture comprises a co-solvent including an organic solvent and an aqueous solvent.