N-acetylcysteine amide (NAC amide) in the treatment of diseases and conditions associated with oxidative stress
Methods and compositions comprising N-acetylcysteine amide (NAC amide) and derivatives thereof are used in treatments and therapies for human and non-human mammalian diseases, disorders, conditions and pathologies. Pharmaceutically or physiologically acceptable compositions of NAC amide or derivatives thereof are administered alone, or in combination with other suitable agents, to reduce, prevent, or counteract oxidative stress and free radical oxidant formation and overproduction in cells and tissues, as well as to provide a new source of glutathione.
1. A dosage form for ophthalmic administration comprising
(a) a therapeutically effective dose of N-acetylcysteine amide (NAC Amide), or a pharmaceutically acceptable sale or ester thereof; and
(b) an ophthalmically acceptable vehicle or carrier;
wherein the dosage form comprises about 25 mg to about 500 mg NAC Amide.
2. The dosage form of claim 1 , comprising about 50 mg to about 350 mg NAC Amide.
3. The dosage form of claim 1 , comprising about 50 mg to about 150 mg NAC Amide.
4. The dosage form of claim 1 , comprising about 25 mg to about 250 mg NAC Amide.
5. The dosage form of claim 1 , comprising about 50 mg NAC Amide.
6. The dosage form of claim 1 , wherein the dosage form is in the form of an eyedrop.
7. The dosage form of claim 1 , wherein the opthalmically acceptable vehicle or carrier comprises a composition selected from the group consisting of water, phosphate buffered saline (pH 7.4), 0.15M aqueous sodium chloride solution and combinations thereof.
8. A method of treating an ophthalmic disease or condition in a subject in need thereof, wherein the method comprises administering a dosage form for ophthalmic administration, wherein the dosage form comprises:
(a) a therapeutically effective dose of N-acetylcysteine amide (NAC Amide), or a pharmaceutically acceptable salt or ester thereof; and
(b) an ophthalmically acceptable vehicle or carrier; and
wherein the ophthalmic disease or condition is macular degeneration.
9. The method of claim 8 , comprising about 25 mg to about 500 mg NAC Amide.
10. The method of claim 8 , comprising about 50 mg to about 350 mg NAC Amide.
11. The method of claim 8 , comprising about 50 mg to about 150 mg NAC Amide.
12. The method of claim 8 , comprising about 25 mg to about 250 mg NAC Amide.
13. The method of claim 8 , comprising about 50 mg NAC Amide.
14. The method of claim 8 , wherein the dosage form is in the form of an eyedrop.
15. The method of claim 8 , wherein the opthalmically acceptable vehicle or carrier comprises a composition selected from the group consisting of water, phosphate buffered saline (pH 7.4), 0.15M aqueous sodium chloride solution and combinations thereof.