Sustained release of microcrystalline peptide suspensions
A fluid, milky microcrystalline aqueous suspension of a peptide or peptidomimetic and a counter-ion of a strong proton donor in water, wherein the peptide or peptidomimetic and counter-ion are present in amounts and at a molar ratio sufficient to form the suspension upon mixing and without formation of a gel. Also, lyophilized compositions that include a dried suspension, methods of making the lyophilized composition, methods of preparing the suspension, and sustained release formulations prepared by the methods.
1. A fluid, milky microcrystalline aqueous suspension comprising a hydrophobic peptide and trifluoroacetic acid, wherein the peptide is a GnRH antagonist selected from the group consisting of Azaline B, Abarelix, Antide, Ganirelix, Cetrorelix, FE200486, or Ac-D-Nal-D-Cpa-D-Pal-Ser-Tyr-D-Hci-Leu-Ilys-Pro-D-Ala-NH 2 , and the peptide salt is present in amounts and at a molar ratio sufficient to form, upon mixing with water, the suspension without formation of a gel.
2. The suspension of claim 1 in which the GnRH antagonist is Ac-D-Nal-D-Cpa-D-Pal-Ser-Tyr-D-Hci-Leu-Ilys-Pro-D-Ala-NH 2 trifluoroacetate.
3. The suspension of claim 1 in which the hydrophobic peptide salt is suspended in the aqueous medium at a concentration of equal to or higher than 25 mg/ml.
4. The suspension of claim 1 in which the aqueous suspension contains an isotonic agent.
5. The suspension of claim 4 in which the isotonic agent is mannitol.
6. The suspension of claim 1 in which the aqueous suspension contains a pharmaceutically acceptable excipient.
7. The suspension of claim 1 wherein the microcrystals are in the form of needles having a particle size of between about 5 and 150 μm.
8. A lyophilized composition comprising the dried suspension of claim 1 .
9. A method of preparing a lyophilized composition which comprises freeze-drying or spray-drying suspension according to claim 1 to obtain the composition.
10. A method of preparing an injectable fluid, milky, microcrystalline aqueous suspension of a hydrophobic peptide which comprises reconstituting with water or a buffer solution the lyophilized composition of claim 8 .
11. A method of preparing a sustained release formulation of a hydrophobic peptide which comprises providing the peptide in the suspension of claim 1 .
12. The method of claim 11 in which the GnRH antagonist is Ac-D-Nal-D-Cpa-D-Pal-Ser-Tyr-D-Hci-Leu-Ilys-Pro-D-Ala-NH 2 trifluoroacetate.
13. The method of claim 11 in which the hydrophobic peptide salt is suspended in the aqueous medium at a concentration of equal to or higher than 25 mg/ml.
14. The method of claim 11 in which the aqueous suspension contains an isotonic agent.
15. The method of claim 14 in which the isotonic agent is mannitol.
16. The method of claim 11 in which the aqueous suspension contains a pharmaceutically acceptable excipient.
17. The method of claim 11 in which the aqueous suspension is obtained extemporaneously from a lyophilized peptide salt.
18. A method of preventing gel formation while producing the aqueous suspension of claim 1 , which comprises forming a salt by contacting the hydrophobic peptide with trifluoroacetic acid.
19. The suspension of claim 1 in which the peptide antagonist is Abarelix.
20. The suspension of claim 19 comprising the hydrophobic peptide salt is suspended in the aqueous medium at a concentration of equal to or higher than 25 mg/ml.
21. The suspension of claim 2 comprising the hydrophobic peptide salt is suspended in the aqueous medium at a concentration of equal to or higher than 25 mg/ml.