Risperidone sustained release microsphere composition
A risperidone sustained release microsphere formulation is provided. The microsphere formulation includes risperidone or 9-hydroxy risperidone or salts thereof, and a polymer blend having a first uncapped lactide-glycolide copolymer and a second uncapped lactide-glycolide copolymer, in which the first uncapped lactide-glycolide copolymer is a copolymer with a high intrinsic viscosity and the second uncapped lactide-glycolide copolymer is a copolymer with a low intrinsic viscosity. The sustained release micro sphere formulation according to an embodiment of the present disclosure is suitable for large-scale industrialized production with improved stability, the in vivo release behavior of which will not change after long-term storage.
1. Microspheres for sustained release of an active agent comprising:
an active agent selected from the group consisting of risperidone, 9-hydroxy risperidone, and a salt thereof; and
a polymer blend consisting of a first uncapped poly(lactide-co-glycolide) having a first carboxyl terminal group and a second uncapped poly(lactide-co-glycolide) having a second carboxyl terminal group;
wherein the first uncapped poly(lactide-co-glycolide) has a molecular weight from 55,000 to 85,000 and a molar ratio of lactide to glycolide in a range from 65:35 to 90:10;
wherein the second uncapped poly(lactide-co-glycolide) has a molecular weight from 15,000 to 35,000 and a molar ratio of lactide to glycolide in a range from 50:50 to 75:25;
wherein a weight ratio of the first uncapped poly(lactide-co-glycolide) to the second uncapped poly(lactide-co-glycolide) is in a range from 50:50 to 95:5; and
wherein the active agent is encapsulated in the polymer blend and the active agent is in an amount of from 10% to 60% based on a total weight of the microspheres.
2. The microspheres of claim 1 ,
wherein no crystals of the active agent are precipitated on the surfaces of microspheres.
3. The microspheres of claim 1 ,
wherein the molar ratio of lactide to glycolide in the first uncapped poly(lactide-co-glycolide) is 75:25; and
wherein the molar ratio of lactide to glycolide in the second uncapped poly(lactide-co-glycolide) is 50:50.
4. The microspheres of claim 1 ,
wherein the weight ratio of the first uncapped poly(lactide-co-glycolide) to the second uncapped poly(lactide-co-glycolide) is in range from 70:30 to 90:10.
5. The microspheres of claim 4 ,
wherein the weight ratio of the first uncapped poly(lactide-co-glycolide) to the second uncapped poly(lactide-co-glycolide) is 80:20.
6. The microspheres of claim 1 ,
Wherein the active agent is encapsulated in the polymer blend and the active agent is in an amount of from 35% to 55% based on a total weigh of microspheres.
7. The microspheres of claim 6 ,
wherein the active agent is encapsulated in the polymer blend and the active agent is in an amount of from 40% to 50% based on a total weigh of microspheres.
8. The microspheres of claim 1 ,
wherein the first uncapped poly(lactide-co-glycolide) has an intrinsic viscosity of 0.4-0.9 dg, and the second uncapped poly(lactide-co-glycolide) has an intrinsic viscosity of 0.1-0.35 dl/g.
9. The microspheres of claim 8 ,
wherein the first uncapped poly(lactide-co-glycolide) has an intrinsic viscosity of 0.45-0.55 dl/g, and the second uncapped poly(lactide-co-glycolide) has an intrinsic viscosity of 0.2-0.3 dl/g.
10. The microspheres of claim 1 ,
wherein the weight content of risperidone is 45%,
wherein the weight ratio of the first uncapped PLGA to the second uncapped PLGA is 80:20;
wherein the molar ratio of lactide to glycolide in the first uncapped PLGA is 75:25 and the molar ratio of lactide to glycolide in the second uncapped PLGA is 50:50; and
wherein an intrinsic viscosity of the first uncapped PLGA is from 0.45 to 0.55 dL/g and an intrinsic viscosity of the second uncapped PLGA is from 0.2 to 0.3 dL/g.
11. The microspheres of claim 1 , wherein the salt of risperidone or the salt of 9-hydroxy risperidone is selected from an inorganic acid salt and an organic acid salt;
wherein the inorganic acid salt is selected from the group consisting of hydrochlorate, hydrobromate, nitrate, sulfate, and phosphate; and
wherein the organic acid salt is selected from the group consisting of acetate, propionate, hydroxy acetate, 2-hydroxy propionate, pamoate, 2-oxo propionate, oxalate, malonate, succinate, 2-butenedioate, methanesulfonate, ethanesulfonate, benzenesulfonate, and toluenesulfonate.
12. A pharmaceutical formulation for injection into a patient in need, comprising: the microspheres of claim 1 and a pharmaceutically acceptable dispersion solvent.
13. The pharmaceutical formulation of claim 12 ,
further comprising mannitol.
14. Microspheres for sustained release of an active agent comprising:
an active agent selected from the group consisting of risperidone, 9-hydroxy risperidone, and a salt thereof; and
a polymer blend consisting of a first uncapped poly(lactide-co-glycolide) having a first carboxyl terminal group and a second uncapped poly(lactide-co-glycolide) having a second carboxyl terminal group;
wherein the first uncapped poly(lactide-co-glycolide) has a weight average molecular weight of 50,000-145,000, an intrinsic viscosity of 0.4-0.9 dl/g, and a molar ratio of lactide to glycolide in a range from 65:35 to 90:10;
wherein the second uncapped poly(lactide-co-glycolide) has a weight average molecular weight of 4,000 to 45,000, an intrinsic viscosity of 0.1-0.35 dl/g, and a molar ratio of lactide to glycolide in a range from 50:50 to 75:25;
wherein a weight ratio of the first uncapped poly(lactide-co-glycolide) to the second uncapped poly(lactide-co-glycolide) is in a range from 50:50 to 95:5; and
wherein the active agent is encapsulated in the polymer blend.
15. The microspheres of claim 14 ,
wherein the first uncapped poly(lactide-co-glycolide) has a weight average molecular weight of 55,000-110,000, and the second uncapped poly(lactide-co-glycolide) has a weight average molecular weight of 4,000-35,000.
16. The microspheres of claim 14 ,
wherein the active agent is in an amount of from 10% to 60% based on a total weight of the microspheres.
17. A method of preparing the microspheres of claim 1 , comprising:
a) dissolving the active agent and the polymer blend in an organic solvent;
b) a mixture from step a) is added into an aqueous solution comprising a water soluble polymer for emulsification;
c) the organic solvent is removed;
d) a residue from step c) is washed and filtered to obtain the microspheres.
18. The method of claim 17 ,
wherein the organic solvent is dichloromethane, and
wherein the water soluble polymer is polyvinyl alcohol.
19. A method of treating a psychosis comprising: administering the pharmaceutical formulation of claim 12 ,
wherein the psychosis is selected from the group consisting of acute schizophrenia, chronic schizophrenia, significant positive symptoms or significant negative symptoms of other psychotic states, and affective symptoms related to schizophrenia.