Non-aqueous injectable formulations for extended release of somatotropin
View Patent ↗The present invention provides compositions which allow for the extended release and enhanced bioavailability of biologically-active polypeptides following parenteral delivery to an animal. More particularly, it concerns compositions comprising biologically-active somatotropin formulated for extended release, methods of preparing these compositions, and methods of using the same. These compositions comprise somatotropin, a bioavailability-enhancing constituent (BEC), and a substantially non-aqueous, hydrophobic excipient. The BEC may comprise (i) amino acids or amino acid derivatives, such as histidine-HCl; (ii) hydroxamate derivatives, such as histidine hydroxamate or suberohydroxamic acid; (iii) non-reducing carbohydrates, such as trehalose or trehalose octaacetate; (iv) oxo-acid salts, such as a mixture of monobasic and dibasic sodium phosphate; or (v) a mixture of two or more compounds from within the foregoing classes (i)–(iv).
1. A method for administering somatotropin to a mammal that comprises injecting into a mammal a composition of matter comprising:
samatotropin and a bioavailability enhancing constituent;
wherein the bioavailability enhancing constituent comprises the following:
a) one or more non-reducing carbohydrates, and/or
b) one or more oxo-acid salts;
wherein the somatotropin and the bioavailability enhancing constituent are suspended in a substantially non-aqueous hydrophobic carrier; wherein the somatotropin is present from about 10% to about 50% by weight of the composition; wherein the bioavailability enhancing constituent is present from about 1% to about 20% by weight of the composition; and wherein the composition is fluidly injectable at 25° C.
2. The method of claim 1 , wherein the bioavailability enhancing constituent is an oxo-acid or a mixture of oxo-acids, present in the composition at from about 0.5% to about 30% by weight, and the hydrophobic carrier is present in the composition at from about 40% to about 90% by weight.
3. The method of claim 1 wherein the composition of matter is injected into a lactating mammal to sustain an elevated milk production response in the mammal.
4. The method of claim 1 wherein the somatotropin is human, equine, bovine, or porcine somatotropin.
5. The method claim 1 , wherein the bioavailability enhancing constituent is non-reducing carbohydrate selected from the group consisting of: at least one polyol, at least one carbohydrate ester, and mixtures thereof.
6. The method of claim 1 , wherein the bioavailability enhancing constituent comprises non-reducing carbohydrate; wherein the non-reducing carbohydrate is polyol present at from about 5% to about 20% by weight of the composition.
7. The method of claim 1 , wherein the bioavailability enhancing constituent comprises at least one oxo-acid salt.
8. The composition of claim 7 , wherein the oxo-acid salt is selected from one or a mixture of two or more of the following: monobasic sodium phosphate, dibasic sodium phosphate, monobasic potassium phosphate, dibasic potassium phosphate, monobasic calcium phosphate, dibasic calcium phosphate, sodium nitrate, dibasic sodium sulfate, and mixtures thereof.
9. The composition of matter of claim 1 , wherein the hydrophobic carrier comprises an oil or a fat.
10. The composition of matter of claim 1 , wherein the somatotropin is a zinc salt of bovine somatotropin present at from about 32% to about 42% by weight;
wherein the bioavailability enhancing constituent is a mixture of monobasic sodium phosphate and dibasic sodium phosphate salts, wherein the molar ratio of monobasic sodium phosphate to dibasic sodium phosphate is about 6 to 4, present at from about 2% to about 10% by weight.
11. The method of claim 3 wherein the mammal is a dairy cow.
12. The method of claim 3 wherein the somatotropin is human, equine, bovine, or porcine.
13. The method claim 3 , wherein the bioavailability enhancing constituent is non-reducing carbohydrate selected from the group consisting of: at least one polyol, at least one carbohydrate ester, and mixtures thereof.
14. The method of claim 3 , wherein the bioavailability enhancing constituent comprises non-reducing carbohydrate; wherein the non-reducing carbohydrate is polyol present at from about 5% to about 20% by weight of the composition.
15. The method of claim 3 , wherein the bioavailability enhancing constituent comprises at least one oxo-acid salt.
16. The composition of claim 3 , wherein the oxo-acid salt is selected from one or a mixture of two or more of the following: monobasic sodium phosphate) dibasic sodium phosphate, monobasic potassium phosphate, dibasic potassium phosphate, monobasic calcium phosphate, dibasic calcium phosphate, sodium nitrate, dibasic sodium sulfate, and mixtures thereof.
17. The composition of matter of claim 3 , wherein the hydrophobic carrier comprises an oil or a fat.
18. The composition of matter of claim 3 , wherein the somatotropin is a zinc salt of bovine somatotropin present at from about 32% to about 42% by weight;
wherein the bioavailability enhancing constituent is a mixture of monobasic sodium phosphate and dibasic sodium phosphate salts, wherein the molar ratio of monobasic sodium phosphate to dibasic sodium phosphate is about 6 to 4, present at from about 2% to about 10% by weight.