Dry powder formulations of antihistamine for nasal administration
View Patent ↗Dry powder formulations of drugs such as antihistamine for nasal administration are provided where the drug is retained in the nasal cavity, and systemic side effects minimized or eliminated, through the selection of a narrow particle size range, between approximately 10 and 20 microns in diameter. In a preferred embodiment wherein the drug is an antihistamine, retention of the antihistamine at the nasal mucosa is improved and the bitter aftertaste associated with liquid antihistamine formulations significantly reduced. By making a dry powder formulation of an antihistamine (e.g., azelastine) having an average particle size of between 10 and 20 microns, the antihistamine is restricted primarily to the desired target organ, the nasal mucosa. Because the active ingredient stays in the nasal region, a lower dose can be used to achieve the same desired effect. As demonstrated by the examples, this lower dose reduces the incidence of somnolence, and because the active ingredient remains at the target organ and does not accumulate in the back of the throat and mouth, this formulation does not impart a bitter taste.
1. A composition for the nasal administration of a drug to a patient comprising a drug in a dry powder form in a dosage formulation suitable for administration to the nasal mucosa, the dry powder made by a process comprising the following steps:
providing preformed diketopiperazine microparticles between 10 and 20 microns in diameter;
suspending said diketopiperazine microparticles in an aqueous medium with a drug to form a suspension; and
forming drug-coated diketopiperazine microparticles by removing solvent from said suspension,
wherein said drug-coated diketopiperazine microparticles are between about 10 and about 20 microns in diameter, more than 50% of the particles have a size greater than about 10 microns, and wherein said particles are maximally retained in the nasal cavity.
2. The composition of claim 1 wherein the drug is selected from the group consisting of antihistamines, vasoconstrictors, antiinflammatories and analgesics.
3. The composition of claim 2 wherein the antihistamine is selected from the group consisting of chlorpheniramine and azelastine.
4. The composition of claim 1 wherein the drug is formulated in a polymeric carrier.
5. A drug delivery device for nasal administration comprising:
a drug in a dry powder form comprising diketopiperazine microparticles coated with said drug wherein said drug-coated diketopiperazine microparticles have an average particle size of between about 10 and about 20 microns in diameter, more than 50% of the particles have a size greater than about 10 microns, and wherein said particles are maximally retained in the nasal cavity; and
a device for delivering a measured dose of the drug to the nasal mucosa.
6. The device of claim 5 wherein the device is a nasal insufflator.
7. The device of claim 5 wherein the drug is selected from the group consisting of antihistamines, vasoconstrictors, antiinflammatories and analgesics.
8. The device of claim 7 wherein the antihistamine is selected from the group consisting of chlorpheniramine and azelastine.
9. The device of claim 5 wherein the drug is formulated in a polymeric carrier.
10. A method of administering a drug to the nasal mucosa of a patient in need thereof, comprising
nasally administering the dry powder drug-coated diketopiperazine microparticles of claim 1 in a dosage formulation suitable for nasal administration wherein said particles are maximally retained in the nasal cavity and said drug does not impart a bitter aftertaste in said patient.
11. The method of claim 10 wherein the drug is selected from the group consisting of antihistamines, vasoconstrictors, antiinflammatories and analgesics.
12. The method of claim 11 wherein the antihistamine is selected from the group consisting of chlorpheniramine and azelastine.
13. The method of claim 10 wherein the drug is formulated in a polymeric carrier.