Oral solutions comprising lisdexamfetamine salts
Oral pharmaceutical solution comprising a pharmaceutically acceptable salt of lisdexamfetamine, and a pharmaceutically acceptable aqueous carrier comprising a buffer and a cosolvent selected from the group consisting of a glycol, a polyol, and a mixture thereof, wherein the pH of the solution is from 5.5 to 9.0. The oral pharmaceutical solution presents excellent physicochemical stability, even under alkaline conditions.
1 . An oral pharmaceutical solution comprising 10 mg/ml of lisdexamfetamine dimesylate and a pharmaceutically acceptable aqueous carrier comprising a buffer and a cosolvent, wherein the pH of the solution is from 6.0 to 9.0 and wherein the cosolvent comprises a glycol.
2 . The oral pharmaceutical solution according to claim 1 , wherein the cosolvent comprises propylene glycol, low molecular weight polyethylene glycol, or a mixture thereof and wherein the total concentration of the cosolvent is from 5 mg/ml to 300 mg/ml.
3 . The oral pharmaceutical solution according to claim 1 , wherein the cosolvent comprises low molecular weight polyethylene glycol.
4 . The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the cosolvent is from 5 mg/ml to 300 mg/ml.
5 . The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the cosolvent is from 50 mg/ml to 250 mg/ml.
6 . The oral pharmaceutical solution according to claim 1 , wherein the total concentration of the cosolvent is from 100 mg/ml to 200 mg/ml.
7 . The oral pharmaceutical solution according to claim 1 , wherein the pH of the solution is from 6.0 to 8.5.
8 . The oral pharmaceutical solution according to claim 1 , wherein the pH of the solution is from 6.5 to 8.0.
9 . The oral pharmaceutical solution according to claim 1 , wherein the cosolvent comprises propylene glycol.
10 . The oral pharmaceutical solution according to claim 1 , wherein the cosolvent further comprises glycerol, sorbitol, or xylitol.
11 . The oral pharmaceutical solution according to claim 7 , wherein the cosolvent comprises low molecular weight polyethylene glycol.
12 . The oral pharmaceutical solution according to claim 7 , wherein the cosolvent comprises propylene glycol.
13 . The oral pharmaceutical solution according to claim 7 , wherein the cosolvent further comprises glycerol, sorbitol, or xylitol.
14 . The oral pharmaceutical solution according to claim 1 , wherein the buffer comprises ascorbic acid, acetic acid, tartaric acid, citric acid monohydrate, sodium citrate, potassium citrate, acetic acid, sodium acetate, sodium hydrogen phosphate, sodium dihydrogen phosphate, calcium hydrogen phosphate, calcium dihydrogen phosphate or mixtures thereof.
15 . The oral pharmaceutical solution according to claim 1 , wherein the buffer comprises a phosphate buffer solution.
16 . The oral pharmaceutical solution according to claim 7 , wherein the buffer comprises ascorbic acid, acetic acid, tartaric acid, citric acid monohydrate, sodium citrate, potassium citrate, acetic acid, sodium acetate, sodium hydrogen phosphate, sodium dihydrogen phosphate, calcium hydrogen phosphate, calcium dihydrogen phosphate or mixtures thereof.
17 . The oral pharmaceutical solution according to claim 7 , wherein the buffer comprises a phosphate buffer solution.
18 . The oral pharmaceutical solution according to claim 12 , wherein the buffer comprises ascorbic acid, acetic acid, tartaric acid, citric acid monohydrate, sodium citrate, potassium citrate, acetic acid, sodium acetate, sodium hydrogen phosphate, sodium dihydrogen phosphate, calcium hydrogen phosphate, calcium dihydrogen phosphate or mixtures thereof.
19 . The oral pharmaceutical solution according to claim 12 , wherein the buffer comprises a phosphate buffer solution.
20 . The oral pharmaceutical solution according to claim 15 , wherein the solution further comprises an antimicrobial preservative.