PHARMACEUTICAL COMPOSITIONS COMPRISING BUPROPION AND CYSTEINE
This disclosure relates to pharmaceutical compositions comprising bupropion and cysteine, and pharmaceutical dosage forms comprising bupropion and cysteine. The disclosure also relates to molecular complexes of bupropion and cysteine. These compositions and dosage forms may have improved stability of bupropion.
1 . A method of treating depression in a human being in need thereof with a dosage form comprising dextromethorphan, bupropion and cysteine, comprising orally administering the dosage form comprising the dextromethorphan, the bupropion, and the cysteine, wherein the dosage form comprises about 33 mg of the dextromethorphan free base, about 91 mg of the bupropion free base, and a cysteine in the neutral form, wherein the dosage form has a molar ratio of the bupropion to the cysteine that is about 0.5:1 to about 1.1:1, wherein bupropion and dextromethorphan are the only therapeutic active agents in the dosage form, wherein the dosage form is a bilayer dosage form, and wherein the bupropion and the cysteine are in a first layer and the dextromethorphan is in a second layer.
2 . The method of claim 1 , wherein the dosage form has a molar ratio of the bupropion to the cysteine that is about 0.7:1 to about 1.1:1.
3 . The method of claim 1 , wherein the molar ratio of the bupropion to the cysteine is about 1:1.
4 . The method of claim 1 , wherein about 40 mg to about 50 mg of the neutral form of cysteine is present in the dosage form.
5 . The method of claim 1 , wherein the dosage form further comprises an extended release polymer.
6 . The method of claim 5 , wherein the extended release polymer is an acrylate polymer or copolymer, a methylcellulose, or a combination thereof.
7 . The method of claim 1 , wherein the dosage form is in the form of a capsule, pill, or tablet.
8 . The method of claim 1 , wherein the dosage form further comprises a filler.
9 . The method of claim 8 , wherein the filler is microcrystalline cellulose.
10 . The method of claim 1 , wherein the dosage form further comprises a lubricant.
11 . The method of claim 10 , wherein the lubricant is magnesium stearate.
12 . The method of claim 1 , wherein the cysteine is L-cysteine monohydrate.
13 . The method of claim 1 , wherein the dosage form comprises a molecular complex of bupropion and cysteine.
14 . The method of claim 13 , wherein the bupropion in the dosage form is more stable than bupropion alone.
15 . The method of claim 1 , wherein the bupropion in the dosage form is more stable than bupropion alone.
16 . The method of claim 1 , wherein the dextromethorphan is in an immediate-release formulation.
17 . The method of claim 16 , wherein the bupropion is in an extended-release formulation.
18 . The method of claim 13 , wherein the molar ratio of the bupropion to the cysteine in the molecular complex is about 1:1.
19 . The method of claim 7 , wherein the dosage form is a tablet.
20 . The method of claim 19 , wherein the dosage form further comprises carbomer homopolymer, colloidal silicon dioxide, crospovidone, glyceryl monocaprylocaprate, magnesium stearate, microcrystalline cellulose, polyvinyl alcohol, red iron oxide, sodium lauryl sulfate, stearic acid, talc, titanium dioxide, yellow iron oxide, or a combination thereof.