Modified release compositions of a GAMMA-hydroxybutyric acid derivative
Pharmaceutical granulations having a functional coating surrounding a core containing 4-((L-valyl)oxy)butanoic acid are disclosed. The functional coatings provide for immediate release or modified release of 4-((L-valyl)oxy)butanoic acid. The pharmaceutical granulations can be used in oral pharmaceutical compositions.
1. A pharmaceutical composition comprising:
(a) an immediate release component, wherein the immediate release component comprises:
a plurality of immediate release granules, wherein the immediate release granules comprise greater than 80 wt % of 4-((L-valyl)oxy)butanoic acid, wherein wt % is based on the total weight of the immediate release granules; and
(b) a modified release component, wherein the modified release component comprises a plurality of modified release granules, wherein,
the modified release granules comprise a core and a modified release coating surrounding the core; and
the core comprises greater than 80 wt % of 4-((L-valyl)oxy)butanoic acid, wherein wt % is based on the total weight of the core.
2. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises from 0.1 g to 20 g of 4-((L-valyl)oxy)butanoic acid.
3. The pharmaceutical composition of claim 1 , wherein,
the immediate release component comprises from 2 g to 4 g of 4-((L-valyl)oxy)butanoic acid; and
the modified release component comprises from 8 g to 16 g of 4-((L-valyl)oxy)butanoic acid.
4. The pharmaceutical composition of claim 1 , wherein the immediate release granules comprise a seal coating.
5. The pharmaceutical composition of claim 4 , wherein the seal coating comprises:
from 65 wt % to 95 wt % of a water soluble polymer; and
from 5 wt % to 35 wt % of an antistatic agent,
wherein wt % is based on the total weight of the seal coating.
6. The pharmaceutical composition of claim 1 , wherein the immediate release granules have an average diameter from 75 μm to 450 μm, wherein the average diameter is determined by sieve analysis or by laser diffraction.
7. The pharmaceutical composition of claim 1 , wherein the modified release granules have an average diameter from 150 μm to 400 μm, wherein the average diameter is determined by sieve analysis or by laser diffraction.
8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises from 10 g to 20 g of 4-((L-valyl)oxy)butanoic acid.
9. The pharmaceutical composition of claim 1 , wherein,
the immediate release component comprises from 10 wt % to 50 wt % of 4-((L-valyl)oxy)butanoic acid; and
the modified release component comprises from 50 wt % to 90 wt % of 4-((L-valyl)oxy)butanoic,
wherein wt % is based on the total weight of 4-((L-valyl)oxy)butanoic acid in the pharmaceutical composition.
10. The pharmaceutical composition of claim 1 , wherein a weight ratio of 4-((L-valyl)oxy)butanoic acid in the immediate release component to 4-((L-valyl)oxy)butanoic acid in the modified release component is from 1:1 to 1:4.
11. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises greater than 5 grams of 4-((L-valyl)oxy)butanoic acid.
12. The pharmaceutical composition of claim 1 , wherein a weight ratio of 4-((L-valyl)oxy)butanoic acid in the immediate release component to 4-((L-valyl)oxy)butanoic acid in the modified release component is from 0.3 to 0.6.
13. The pharmaceutical composition of claim 1 , wherein the modified release granules comprise from 10 wt % to 50 wt % of the modified release coating, wherein wt % is based on the total weight of the modified release granules.
14. The pharmaceutical composition of claim 1 , wherein the core comprises from 85 wt % to 95 wt % of γ-((L-valyl)oxy)butanoic acid, wherein wt % is based on the total weight of the core.
15. The pharmaceutical composition of claim 1 , wherein the core comprises:
greater than 85 wt % of γ-((L-valyl)oxy)butanoic acid;
from 1 wt % to 10 wt % of an antistatic agent; and
from 1 wt % to 10 wt % of a water-soluble polymer,
wherein wt % is based on the total weight of the core.
16. The pharmaceutical composition of claim 15 , wherein,
the antistatic agent comprises talc; and
the water-soluble polymer comprises hydroxypropylmethyl cellulose.
17. The pharmaceutical composition of claim 1 , wherein the modified release coating comprises:
from 70 wt % to 95 wt % of a matrix polymer; and
from 5 wt % to 30 wt % of an antistatic agent,
wherein wt % is based on the total weight of the modified release coating.
18. The pharmaceutical composition of claim 17 , wherein the matrix polymer comprises:
from 92 wt % to 98 wt % of a water-insoluble polymer; and
from 2 wt % to 8 wt % of a water-soluble polymer,
wherein wt % is based on the total weight of the matrix polymer.
19. The pharmaceutical composition of claim 18 , wherein,
the water-insoluble polymer comprises ethylcellulose; and
the water-soluble polymer comprises hydroxypropyl cellulose.
20. The pharmaceutical composition of claim 17 , wherein the antistatic agent comprises talc.