Anti-methanogenic compositions and uses thereof
AssigneesCedars-Sinai Medical Center, Synthetic Biologics, Inc.
InventorsMark Pimentel, Ruchi Mathur, Steve Kanzer, Vince Wacher
Life of this patent
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Abstract
The present invention relates to, in part, methods and compositions for the treatment of methanogen-associated disorders such as, for example, Irritable Bowel Syndrome (IBS). Particularly, modified-release formulations comprising at least one antimethanogenic statin are provided which release the antimethanogenic statin in the intestines.
Claims22
A pharmaceutical formulation, comprising at least two types of modified-release particles, each modified-release particle containing:
- about 5-20% by weight antimethanogenic statin;
- about 50-70% by weight microcrystalline cellulose;
- about 1-10% by weight copovidone;
- about 0.1-3.0% by weight silicon dioxide;
- about 0.1-3.0% by weight magnesium stearate;
- about 1-10% by weight crospovidone;
- and
- about 10-20% by weight enteric polymer,
- wherein each modified-release particle comprises about 7 mg of the antimethanogenic statin;
- wherein a first type of modified-release particle comprises a first enteric polymer that dissolves at a pH of about 5.5 and a second type of modified-release particle comprises a second enteric polymer that dissolves at a pH of about 7.0.
A pharmaceutical formulation, comprising:
- about 5-20% by weight of the antimethanogenic statin;
- about 30-60% by weight microcrystalline cellulose;
- about 1-10% by weight copovidone;
- about 0.1-3.0% by weight silicon dioxide;
- about 0.1-3.0% by weight magnesium stearate;
- about 1-10% by weight crospovidone;
- about 0.5-10% by weight a first enteric polymer that dissolves at a pH of about 5.5 and encapsulates a first type particle comprising the antimethanogenic statin;
- about 1-15% by weight a second enteric polymer that dissolves at a pH of about 7.0 and encapsulates a second type particle comprising the antimethanogenic statin;
- wherein each particle comprises about 7 mg of the antimethanogenic statin;
- wherein the first type particle and the second type particle are present in a ratio of about 1:2, such that the formulation has a unit dosage of about 21 mg.
A pharmaceutical formulation, comprising:
- about 5-20% by weight of the antimethanogenic statin;
- about 30-60% by weight microcrystalline cellulose;
- about 1-10% by weight copovidone;
- about 0.1-3.0% by weight silicon dioxide;
- about 0.1-3.0% by weight magnesium stearate;
- about 1-10% by weight crospovidone;
- about 0.5-10% by weight a first enteric polymer that dissolves at a pH of about 5.5 and encapsulates a first type particle comprising the antimethanogenic statin;
- about 1-15% by weight a second enteric polymer that dissolves at a pH of about 7.0 and encapsulates a second type particle comprising the antimethanogenic statin;
- wherein each particle comprises about 7 mg of the antimethanogenic statin;
- wherein the first type particle and the second type particle types are present in a ratio of about 1:5, such that the formulation has a unit dosage of about 42 mg.
Dependencies are inferred from the claim text.