Use of simple amino acids to form porous particles
AssigneeAdvanced Inhalation Research, Inc.
InventorsRichard P. Batycky, Michael M. Lipp, Ralph W. Niven
Life of this patent
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Abstract
Particles having a tap density of less than 0.4 g/cm3 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.
Claims47
A method for drug delivery to the respiratory system comprising:
- administering to the respiratory tract of a patient in need of treatment, prophylaxis or diagnosis an effective amount of particles comprising a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic amino acid or salt thereof;
- wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between about 1 and 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
Particles produced by a method of preparing particles, comprising:
- (a) forming a mixture comprising a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic 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/cm3 wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between about 1 and about 5 microns, an wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
A method comprising administering to the respiratory tract of a patient in need of treatment, prophylaxis or diagnosis an effective amount of particles produced by a method of preparing particles, comprising:
- (a) forming a mixture comprising a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic 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/cm3 wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between about 1 and about 5 microns, an wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
Particles comprising a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic amino acid or salt thereof;
- wherein the particles have a tap density less than about 0.4 g/cm3 wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between about 1 and about 5 microns, an wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
Particles having a tap density of less than about 0.4 g/cm3 comprising a phospholipid and a hydrophobic amino acid or salt thereof and a median aerodynamic diameter of between about 1 and about 5 microns, an wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
A composition for drug delivery to the pulmonary system comprising particles including a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic amino acid or salt thereof, wherein the particles have a tap density of less than 0.4 g/cm3 and a median aerodynamic diameter of between 1 and about 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
A method for drug delivery to the respiratory system comprising:
- administering to the respiratory tract of a patient in need of treatment or prophylaxis or an effective amount of particles comprising a therapeutic, a hydrophobic amino acid or salt thereof, and a phospholipid or combination of phospholipids;
- wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between 1 and about 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
A method for drug delivery to the pulmonary system comprising:
- administering to the respiratory tract of a patient in need of treatment, prophylaxis or diagnosis an effective amount of particles wherein said particles consist of a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic amino acid or salt thereof, and wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between 1 and about 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
A method for drug delivery to the pulmonary system comprising:
- administering to the respiratory tract of a patient in need of treatment, prophylaxis or diagnosis an effective amount of particles wherein said particles consist of a therapeutic, prophylactic or diagnostic agent, or any combination thereof, a hydrophobic amino acid or salt thereof, and a phospholipid or combination of phospholipids and wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between 1 and about 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
Particles comprising a therapeutic, prophylactic or diagnostic agent, or any combination thereof, an amino acid or salt thereof, and a phospholipid or combination of phospholipids;
- wherein the particles have a tap density less than about 0.4 g/cm3.
Particles consisting of a therapeutic, prophylactic or diagnostic agent, or any combination thereof, and a hydrophobic amino acid or salt thereof;
- wherein the particles have a tap density less than about 0.4 g/cm3 and a median aerodynamic diameter of between 1 and about 5 microns, and wherein the amino acid or salt thereof is present in the particles in an amount of at least 10% by weight.
Dependencies are inferred from the claim text.