ORAL ENTERIC ANTIDEPRESSANT FORMULATION
Pharmaceutical presentations of phenoxathiin-based MAO-A inhibitors are disclosed whereby the MAO receptors are protected from binding to active ingredient in the stomach. Particular phenoxathiin-based MAO-A inhibitors include those of the following formula: (I) wherein n is 0, 1 or 2; R1 is a branched or straight chain C1-5 alkyl or C3-6 cycloalkyl optionally substituted with hydroxyl, or one or more halogens; and X 1 , X 2 , X 3 , X 4 , and X 5 are either all hydrogens or one or two of X 1 , X 2 , X 3 , X 4 , and X 5 are halogen and the remainder are hydrogens, with the proviso that when n is 0 or 1 and each X is hydrogen, R 1 is not methyl. A wide variety of enteric mechanisms may be utilized so as to provide release of the active ingredient essentially out of the environment of the stomach after ingestion as a pharmaceutical presentation, such as a tablet or capsule. Presentations include enteric coated tablets, enteric coated capsules, capsules containing enteric coated beads.
1 . An enteric oral pharmaceutical product comprising a phenoxathiin-based MAO-A inhibitor of the following formula:
wherein n is 0, 1 or 2; R 1 is a branched or straight chain C1-5 alkyl or C3-6 cycloalkyl optionally substituted with hydroxyl, or one or more halogens; and X 1 , X 2 , X 3 , X 4 , and X 5 are either all hydrogens or one or two of X 1 , X 2 , X 3 , X 4 , and X 5 are halogen and the remainder are hydrogens, with the proviso that when n is 0 or 1 and each X is hydrogen, R 1 is not methyl.
2 . The enteric product of claim 1 , wherein the phenoxathiin-based MAO-A inhibitor is 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide.
3 . The enteric product of claim 1 , wherein said product is a tablet.
4 . The enteric product of claim 1 , wherein said product is a capsule or a core sheathed in an annular body.
5 . The enteric product of claim 1 , wherein said product comprises an enteric coating which is essentially not dissolvable in the stomach surrounding a core which comprises said active ingredient.
6 . The enteric product of claim 1 , wherein said product contains 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide as the sole active ingredient.
7 . The enteric product of claim 2 , wherein said 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide is characterized as having a melting point at about 169-175° C.
8 . The enteric product of claim 2 wherein said 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide is characterized as being in crystalline form and having an x-ray powder diffraction peak at 2θ=11.0°, using CuK α radiation.
9 . The enteric product of claim 1 , wherein said product comprises:
(a) a core consisting of 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide and one or more pharmaceutical excipients;
(b) an optional separating layer;
(c) an enteric layer comprising hydroxypropylmethylcellulose acetate succinate (HPMCAS) and a pharmaceutically acceptable excipient; and
(d) an optional finishing layer.
10 . The enteric product of claim 9 , wherein the separating layer (b) is present.
11 . The enteric product of claim 9 , wherein the core comprises an inert bead on which the 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide is deposited as a layer comprising said one or more pharmaceutical excipients.
12 . The enteric product of claim 1 , wherein said product is a tablet containing about 50 to 500 milligrams of 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide.
13 . An oral pharmaceutical dosage form comprising 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide and adapted to retard or inhibit the release of 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin 10,10-dioxide in the stomach.
14 . The oral pharmaceutical dosage form of claim 13 that is a tablet, a capsule, or a core sheathed in an annular body.
15 . The pharmaceutical dosage form of claim 14 that is a tablet.
16 . The pharmaceutical dosage form of claim 14 that is a capsule.
17 . The pharmaceutical dosage form of claim 13 comprising an enteric coating.