Stabilizing alkylglycoside compositions and methods thereof
View Patent ↗The present invention relates to alkylglycoside-containing compositions and methods for increasing the stability, reducing the aggregation and immunogenicity, increasing the biological activity, and reducing or preventing fibrillar formation of a peptide, polypeptide, or variant thereof, for example amylin, a monoclonal antibody, insulin, Peptide T or analog thereof, gastrin, gastrir releasing peptides, gastrin releasing peptide-like (GRP) proteins, epidermal growth factor or analog thereof.
1. A liquid pharmaceutical composition for increasing the stability, reducing aggregation or reducing immunogenicity of octreotide or a variant thereof comprising:
octreotide or a variant thereof; and
a stabilizing agent comprising at least one alkylglycoside, with the proviso that the composition is free of naturally occurring variants of octreotide.
2. The composition of claim 1 , further comprising a buffering agent.
3. The composition of claim 1 , wherein the alkylglycoside has an alkyl chain and wherein the alkyl chain has between about 10 to 16 carbon atoms.
4. The composition of claim 1 , wherein the alkylglycoside is selected from the group consisting of dodecyl maltoside, tridecyl maltoside, tetradecyl maltoside, sucrose mono-dodecanoate, sucrose mono-tridecanoate, and sucrose mono-tetradecanoate.
5. The composition of claim 1 , wherein the alkylglycoside has a critical micelle concentration (CMC) of less than about 1 mM.
6. The composition of claim 5 , wherein the alkylglycoside has a CMC of less than about 0.5 mM.
7. The composition of claim 1 , further comprising a mucosal delivery-enhancing agent selected from the group consisting of an aggregation inhibitory agent, a charge-modifying agent, a pH control agent, a degradative enzyme inhibitory agent, a mucolytic or mucus clearing agent, a chitosan, and a ciliostatic agent.
8. The composition of claim 7 , wherein the mucosal delivery-enhancing agent is a chitosan.
9. The composition of claim 7 , wherein the mucosal delivery-enhancing agent is a ciliostatic agent.
10. The composition of claim 1 , further comprising benzalkonium chloride or chloroethanol.
11. The composition of claim 1 , further comprising a membrane penetration-enhancing agent selected from the group consisting of a surfactant, a bile salt, a phospholipid additive, a mixed micelle, a liposome, a carrier, an alcohol, an enamine, a nitric oxide donor compound, a long-chain amphipathic molecule, a small hydrophobic penetration enhancer, a sodium or a salicylic acid derivative, a glycerol ester of acetoacetic acid, a cyclodextrin or beta-cyclodextrin derivative, a medium-chain fatty acid, a chelating agent, an amino acid or salt thereof, an N-acetylamino acid or salt thereof, an enzyme degradative to a selected membrane component and any combination thereof.
12. The composition of claim 1 , further comprising a modulatory agent of epithelial junction physiology.
13. The composition of claim 1 , further comprising a vasodilator agent.
14. The composition of claim 1 , further comprising a selective transport-enhancing agent.
15. The composition of claim 1 , wherein the composition is stable for at least one month when stored at temperatures from about 25 to 37 degrees Celsius.
16. The composition of claim 15 , wherein the composition is stable for at least two months.
17. The composition of claim 1 , wherein the composition is stable for at least one year when stored at about 4 degrees Celsius.
18. The composition of claim 1 , wherein the stability of the composition is determined by determining the bioactivity of octreotide or the variant thereof in an in vivo or in vitro assay.
19. The composition of claim 1 , wherein the composition further comprises a bulking agent selected from the group consisting of albumin, collagen, alginate, and mannitol.
20. The composition of claim 1 , wherein the composition is formulated for intranasal, pulmonary, or buccal delivery.
21. A method for increasing the stability of octreotide or a variant thereof comprising: admixing octreotide or a variant thereof, a stabilizing agent and a buffering agent to form a liquid composition, with the proviso that the composition is free of naturally occurring variants of octreotide, wherein the stabilizing agent is at least one alkylglycoside surfactant, thereby increasing the stability of the octreotide or variant thereof.
22. The method of claim 21 , wherein the alkylglycoside is selected from the group consisting of dodecyl maltoside, tridecyl maltoside, tetradecyl maltoside, sucrose mono-dodecanoate, sucrose mono-tridecanoate and sucrose mono-tetradecanoate.
23. The method of claim 21 wherein the alkylglycoside has a critical micelle concentration (CMC) of less than about 1 mM.
24. The method of claim 23 , wherein the alkylglycoside has a CMC of less than about 0.5 mM.
25. The method of claim 21 , wherein the composition further comprises a mucosal delivery-enhancing agent selected from the group consisting of an aggregation inhibitory agent, a charge-modifying agent, a pH control agent, a degradative enzyme inhibitory agent, a mucolytic or mucus clearing agent, a chitosan, and a ciliostatic agent.
26. The method of claim 25 , wherein the mucosal delivery-enhancing agent is a chitosan.
27. The method of claim 25 , wherein the mucosal delivery-enhancing agent is a ciliostatic agent.
28. The method of claim 21 , wherein the composition further comprises benzalkonium chloride or chloroethanol.
29. The method of claim 21 , wherein the composition further comprises a membrane penetration-enhancing agent selected from the group consisting of a surfactant, a bile salt, a phospholipid additive, a mixed micelle, a liposome, a carrier, an alcohol, an enamine, a nitric oxide donor compound, a long-chain amphipathic molecule, a small hydrophobic penetration enhancer, a sodium or a salicylic acid derivative, a glycerol ester of acetoacetic acid, a cyclodextrin or beta-cyclodextrin derivative, a medium-chain fatty acid, a chelating agent, an amino acid or salt thereof, an N-acetylamino acid or salt thereof, an enzyme degradative to a selected membrane component and any combination thereof.
30. The method of claim 21 , wherein the composition further comprises a modulatory agent of epithelial junction physiology.
31. The method of claim 21 , wherein the composition further comprises a vasodilator agent.
32. The method of claim 21 , wherein the composition further comprises a selective transport-enhancing agent.
33. The method of claim 21 , wherein the composition is stable for at least one month when stored at temperatures from about 25 to 37 degrees Celsius.
34. The method of claim 33 , wherein the composition is stable for at least two months when stored at temperatures from about 25 to 37 degrees Celsius.
35. The method of claim 21 , wherein the composition is stable for at least one year when stored at about 4 degrees Celsius.
36. The method of claim 21 , wherein the stability of the composition is determined by determining the bioactivity of octreotide or the variant thereof in an in vivo or in vitro assay.
37. The method of claim 21 , wherein the composition further comprises a bulking agent selected from the group consisting of albumin, collagen, alginate, and mannitol.