Compositons for nasal administration of pharmaceuticals
View Patent ↗Compositions for nasal administration, which comprise a pharmaceutical, a physiologically active peptide, or a peptide-related compound, and as the carrier thereof, crystalline cellulose with a specific particle diameter and/or partially pregelatinized starch are provided. Such compositions improve the in vivo absorption efficiency of pharmaceuticals.
1. A powdered pharmaceutical composition comprising:
a) a physiologically active peptide or a peptide-related compound, wherein the peptide or peptide-related compound has a molecular weight of 30,000 or less; and
b) a carrier consisting of crystalline cellulose, having a mean sieving particle diameter of less than 50 μm,
wherein when administered intranasally to a primate, at least one pharmacokinetic parameter is improved compared to the pharmacokinetic profile of an intranasally administered powdered pharmaceutical composition comprising a carrier having a mean sieving particle diameter of at least 50 μm.
2. The pharmaceutical composition of claim 1 , wherein the at least one improved pharmacokinetic parameter is a higher area under the curve (AUC) for blood concentration-time profile.
3. The pharmaceutical composition of claim 2 , wherein the higher AUC is from about 1.78 to about 2.78-fold higher.
4. The pharmaceutical composition of claim 1 , wherein the at least one improved pharmacokinetic parameter is a higher maximum blood concentration (C max ).
5. The pharmaceutical composition of claim 4 , wherein the higher C max is from about 1.05 to about 2.72-fold higher.
6. The pharmaceutical composition of claim 1 , wherein the at least one improved pharmacokinetic parameter is an increased amount of time for the drug concentration in blood to decline by half (t 1/2 ).
7. The pharmaceutical composition of claim 1 , wherein two or more pharmacokinetic parameters are improved.
8. The pharmaceutical composition of claim 7 , where the two or more improved pharmacokinetic parameters are selected from the group consisting of higher AUC, higher C max and increased t 1/2 .
9. The pharmaceutical composition of claim 1 , wherein the physiologically active peptide is insulin and wherein the at least one improved pharmacokinetic parameter is a higher AUC.
10. The pharmaceutical composition of claim 1 , wherein the physiologically active peptide is insulin and wherein the at least one improved pharmacokinetic parameter is a higher C max .
11. The pharmaceutical composition of claim 1 , wherein the physiologically active peptide is growth hormone and wherein the at least one improved pharmacokinetic parameter is a higher AUC.
12. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is growth hormone and wherein the at least one improved pharmacokinetic parameter is a higher C max .
13. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is glucagon and wherein the at least one improved pharmacokinetic parameter is a higher AUC.
14. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is glucagon and wherein the at least one improved pharmacokinetic parameter is a higher C max .
15. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is glucagon and wherein the at least one improved pharmacokinetic parameter is an increased t 1/2 .
16. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is calcitonin and wherein the at least one improved pharmacokinetic parameter is a higher AUC.
17. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is calcitonin and wherein the at least one improved pharmacokinetic parameter is a higher C max .
18. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is parathyroid hormone (1-34) and wherein the at least one improved pharmacokinetic parameter is a higher AUC.
19. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is parathyroid hormone (1-34) and wherein the at least one improved pharmacokinetic parameter is a higher C max .
20. The pharmaceutical composition of claim 1 , wherein the physiologically active peptide or peptide related compound is selected from the group consisting of growth hormone, calcitonin, glucagon, parathyroid hormone, parathyroid hormone (1-34), glucagon-like peptide-1, interferon, interleukin, erythropoietin, luteinizing hormone-releasing hormone, somatostatin, vasopressin, oxytocin, enkephalin, adrenocorticotropic hormone, growth hormone-releasing hormone, granulocyte colony formation-stimulating factor, thyroid-stimulating hormone-releasing hormone, angiotensin, prolactin, luteinizing hormone, gastric inhibitory polypeptide (GIP), C-peptide, cyclosporine, and FK-506.
21. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is insulin, growth hormone, calcitonin, glucagon, parathyroid hormone, glucagon-like peptide-1, or parathyroid hormone (1-34).
22. The pharmaceutical composition of claim 1 , comprising the physiologically active peptide, wherein the physiologically active peptide is glucagon-like peptide-1.
23. The pharmaceutical composition of claim 1 , comprising the peptide-related compound, wherein the peptide-related compound is selected from the group consisting of a parathyroid hormone (1-34) related compound comprising at least one peptide bond in the molecular structure, a glucagon-like peptide-1 related compound comprising at least one peptide bond in the molecular structure, and a vasopressin related compound comprising at least one peptide bond in the molecular structure.
24. A powdered pharmaceutical composition comprising:
a) glucagon-like peptide-1; and
b) a carrier consisting of crystalline cellulose having a mean sieving particle diameter of less than 50 μm, wherein when administered intranasally to a primate, at least one pharmacokinetic parameter is improved compared to the pharmacokinetic profile of an intranasally administered powdered pharmaceutical composition comprising glucagon-like peptide-1 and a carrier having a mean sieving particle diameter of at least 50 μm.
25. The pharmaceutical composition of claim 20 , wherein the physiologically active peptide or peptide related compound is FK-506.