STATIN COMPOSITIONS
The present invention relates to an improved statin or salt thereof composition, especially an atorvastatin composition, which exhibits enhanced dissolution properties in acidic media. It comprises a statin active ingredient and an aminoalkyl methacrylate copolymer dispersed therein, such as dimethyl aminoethyl methacrylate. The invention also relates to a process for preparing the improved composition and to methods of using it for the treatment of dyslipidemia.
1 . A statin or salt thereof composition having a dissolution, for a composition containing 80 mg of equivalent statin, in a 1000 ml USP HCl buffer at pH 2.2, using the paddles method at 75 rpm, of at least 40% at 10 minutes, at least 50% at 20 minutes and at least 60% at 60 minutes.
2 . The composition of claim 1 having a dissolution in a 1000 ml USP HCl buffer at pH 2.2, using the paddles method at 75 rpm, of at least 60% at 10 minutes, at least 70% at 20 minutes and at least 80% at 60 minutes.
3 . The composition of claim 1 , comprising between 10 and 40% of statin.
4 . The composition of claim 1 , wherein the statin is at least one ring-opened 7-substituted-3,5-dihydroxyheptanoic acid or ring-opened 7-substituted-3,5-dihydroxyheptenoic acid.
5 . The composition of claim 1 , wherein the statin is selected from the group consisting of lovastatin, mevastatin, simvastatin, pravastatin, atorvastatin, cerivastatin, itavastatin, fluvastatin, pitavastatin, rosuvastatin, and salts thereof.
6 . The composition of claim 1 , wherein the statin is under a salt form.
7 . The composition of claim 1 , under a tablet form.
8 . The composition of claim 1 , wherein the statin or salt thereof is atorvastatin.
9 . The composition of claim 2 , wherein the statin or salt thereof is atorvastatin.
10 . The composition of claim 8 , under a tablet form.
11 . A statin or salt thereof composition comprising at least one aminoalkyl methacrylate copolymer dispersed therein.
12 . The composition of claim 11 , wherein the aminoalkyl methacrylate copolymer is dimethyl aminoethyl methacrylate.
13 . The composition of claim 11 , comprising between 10 and 50 wt % of aminoalkyl methacrylate copolymer.
14 . The composition of claim 11 , comprising between 20 and 40 wt % of aminoalkyl methacrylate copolymer.
15 . The composition of claim 11 , comprising between 10 and 40% of statin.
16 . The composition of claim 11 , wherein the statin is at least one ring-opened 7-substituted-3,5-dihydroxyheptanoic acid or ring-opened 7-substituted-3,5-dihydroxyheptenoic acid.
17 . The composition of claim 11 , wherein the statin is selected from the group consisting of lovastatin, mevastatin, simvastatin, pravastatin, atorvastatin, cerivastatin, itavastatin, fluvastatin, pitavastatin, rosuvastatin, and salts thereof.
18 . The composition of claim 11 , wherein the statin is under a salt form.
19 . The composition of claim 11 , under a tablet form.
20 . The composition of claim 11 , wherein the statin or salt thereof is atorvastatin.
21 . The composition of claim 20 , comprising between 10 and 40% of atorvastatin.
22 . The composition of claim 20 , under a tablet form.
23 . A method for the treatment of dyslipidemia, comprising the step of orally administering to a patient in need of such treatment a therapeutically effective unit dosage of a statin or salt thereof composition comprising at least one aminoalkyl methacrylate copolymer dispersed therein.
24 . A method for the treatment of dyslipidemia, comprising the step of orally administering to a patient in need of such treatment a therapeutically effective unit dosage of statin or salt thereof composition having a dissolution, for a composition containing 80 mg of equivalent statin, in a 1000 ml USP HCl buffer at pH 2.2, using the paddles method at 75 rpm, of at least 40% at 10 minutes, at least 50% at 20 minutes and at least 60% at 60 minutes.
25 . A method for the manufacture of a statin composition, comprising the steps of (i) preparing a granule comprising a statin and at least one aminoalkyl methacrylate copolymer mixed therewith, and (ii) compressing the resulting granule into a tablet.