Implantable device for the sustained release of a polypeptide
View Patent ↗Described herein are implantable devices, formulations and methods of making implantable devices for the release of a polypeptide from an implantable device, and methods of use thereof.
1. An implantable device for the sustained release of a polypeptide, comprising:
a) a homogeneous copolymer matrix that, in a hydrated state, forms a hydrogel with an equilibrium water content value ranging from about 20% to about 85%, wherein the homogeneous copolymer matrix further comprises a release agent of a molecular weight of at least about 1000 Daltons; and
a solid formulation comprising a polypeptide, wherein the solid formulation is substantially encased within the homogeneous copolymer matrix.
2. The implantable device of claim 1 , wherein the release agent comprises a non-ionic surfactant.
3. The implantable device of claim 1 , wherein the release agent is selected from the group consisting of: Brij 35, polyoxyetheylene(20)sorbitan trioleate, Tween 20, Tween 80, Vitamin E TPGS, and combinations thereof.
4. The implantable device of claim 1 , wherein the implantable device has an outer surface area of about 350 mm 2 or greater when in a dry state.
5. The implantable device of claim 4 , wherein the implantable device has an outer surface area ranging from about 350 mm 2 to about 600 mm 2 when in a dry state.
6. The implantable device of claim 1 , wherein the implantable device has an outer surface area of about 500 mm 2 or greater when in a hydrated state.
7. The implantable device of claim 6 , wherein the implantable device has an outer surface area ranging from about 500 mm 2 to about 800 mm 2 when in a hydrated state.
8. The implantable device of claim 1 , wherein the polypeptide comprises a GLP-1 (glucagon-like peptide) analogue.
9. The implantable device of claim 8 , wherein the GLP-1 (glucagon-like peptide) analogue is exenatide.
10. The implantable device of claim 1 , wherein the homogeneous copolymer matrix is formed using a formulation comprising hydroxyethylmethacrylate, ethyleneglycol dimethacrylate, the release agent, water and a lower aliphatic monohydric alcohol.
11. The implantable device of claim 10 , wherein the formulation is selected from the group consisting of
a) about 78.72% HEMA (hydroxyethylmethacrylate), about 0.40% EGDMA (ethyleneglycol dimethacrylate), about 0.79% Vitamin E TPGS, about 0.24% BME (benzoin methyl ether), about 0.08% P-16 (Perkadox® 16), about 9.89% water and about 9.89% isopropyl alcohol;
b) about 78.72% HEMA, about 0.40% EGDMA, about 0.79% Vitamin E TPGS, about 0.24% BME, about 0.08% P-16 and about 19.78% water;
c) about 68.97% HEMA, about 0.35% EGDMA, about 0.69% Vitamin E TPGS, about 0.21% BME, about 0.07% P-16, about 14.85% water and about 14.85% isopropyl alcohol; and
about 68.97% HEMA, about 0.35% EGDMA, about 0.69% Vitamin E TPGS, about 0.21% BME, about 0.07% P-16 and about 29.71% isopropyl alcohol.
12. The implantable device of claim 1 , wherein the solid formulation comprises about 98% exenatide and about 2% stearic acid.
13. A method of delivering a polypeptide to a subject in a sustained release manner, the method comprising inserting an implantable device beneath the subject's skin, wherein the implantable device comprises a homogeneous copolymer matrix comprising a release agent with a molecular weight of at least about 1000 Daltons, and a solid formulation comprising a polypeptide, wherein the solid formulation is substantially encased within the matrix.
14. The method of claim 13 , wherein the implantable device is inserted in a dry state.
15. The method of claim 13 , wherein the implantable device is inserted in a hydrated state.
16. The method of claim 13 , wherein the implantable device provides a sustained release of the polypeptide over a period of at least about two months.
17. The method of claim 13 , wherein the release agent comprises a non-ionic surfactant.
18. The method of claim 17 , wherein the release agent is selected from the group consisting of: Brij 35, polyoxyetheylene(20)sorbitan trioleate, Tween 20, Tween 80, Vitamin E TPGS, and combinations thereof.
19. The method of claim 13 , wherein the implantable device has an outer surface area of about 350 mm 2 or greater when in a dry state.
20. The method of claim 19 , wherein the implantable device has an outer surface area ranging from about 350 mm 2 to about 600 mm 2 when in a dry state.
21. The method of claim 13 , wherein the implantable device has an outer surface area of about 500 mm 2 or greater when in a hydrated state.
22. The method of claim 21 , wherein the implantable device has an outer surface area ranging from about 500 mm 2 to about 800 mm 2 when in a hydrated state.
23. The method of claim 13 , wherein the polypeptide comprises a GLP-1 analogue.
24. The method of claim 23 , wherein the GLP-1 analogue is exenatide.
25. The method of claim 13 , wherein the homogeneous copolymer matrix is formed using a formulation comprising hydroxyethylmethacrylate, ethyleneglycol dimethacrylate, the release agent, water and a lower aliphatic monohydric alcohol.
26. The method of claim 25 , wherein the solid formulation comprises about 98% exenatide and about 2% stearic acid.
27. The method of claim 13 , wherein the subject is diabetic or in need of glycemic control.