Enteric soft capsules comprising polyunsaturated fatty acids
View Patent ↗Described herein are pharmaceutical compositions comprising polyunsaturated fatty acids and methods of manufacturing the same. In particular, described herein are pharmaceutical compositions comprising soft enteric capsules comprising omega-3 polyunsaturated fatty acids. The oral pharmaceutical compositions described herein are useful as nutritional supplements or for the treatment of cardiovascular-related diseases, such as hyper dyslipidemia and high triglyceride levels.
1. A method for treating or reducing symptoms of a cardiovascular-related disease comprising administering to a subject in need thereof an oral pharmaceutical dosage form comprising an enteric soft capsule shell comprising:
gelatin and an enteric polymer;
wherein a weight ratio of enteric polymer to gelatin is 1:2.6; and
the shell encapsulates a fill comprising at least 70% by weight eicosapentaenoic free fatty acid (EPA), wherein upon administration, the enteric soft capsule reduces onset or ameliorates symptoms of gastrointestinal side effects comprising one or more of eructation, abdominal discomfort, nausea, diarrhea or fishy odor.
2. The method of claim 1 , wherein the cardiovascular related disease comprises hyperlipidemia, hypertriglyceridemia, hypertension, hypercholesterolemia, mixed dyslipidemia, sitosterolemia, atherosclerosis, or a combination thereof.
3. The method of claim 1 , wherein the enteric soft capsule exhibits an in vitro dissolution rate at pH 6.8 comprising about 50% dissolution after about 20 minutes.
4. The method of claim 1 , wherein the dosage form comprises 70% by weight EPA free fatty acid.
5. The method of claim 1 , wherein the dosage form comprises about 30% by weight DHA.
6. The method of claim 5 , wherein the DHA is a free fatty acid.
7. The method of claim 1 , wherein the dosage from comprises about 250 mg of omega-3 polyunsaturated fatty acid.
8. The method of claim 1 , wherein the administration comprises two dosage forms per day.
9. The method of claim 1 , wherein administration of a 500 mg dose achieves one or more of the following pharmacokinetic parameters:
(a) a mean plasma EPA AUC 0→12 of about 1000 h·mg/L to about 3000 h·mg/L;
(b) a mean plasma DHA C max of about 100 mg/L to about 250 mg/L; or
(c) a mean plasma DHA AUC 0→12 of about 800 h·mg/L to about 3000 h·mg/L.
10. The method of claim 1 , wherein the dosage form comprises a weight ratio of EPA to DHA of about 2.5:1 to about 3:1.
11. The method of claim 1 , wherein dosage form further comprises a plasticizer, an alkali neutralizing agent, and a solvent.
12. The method of claim 11 , wherein the enteric polymer is an acrylic and methacrylic acid copolymer; the plasticizer is glycerol or triethyl citrate or a combination thereof; the alkali neutralizing agent is ammonium hydroxide or sodium hydroxide or a combination thereof; and the solvent is water.
13. The method of claim 1 , wherein the dosage form further comprises a fat soluble vitamin comprising vitamin A, vitamin D, vitamin E, or vitamin K.
14. The method of claim 13 , wherein the fat soluble vitamin comprises cholecalciferol (vitamin D).
15. The method of claim 1 , wherein the gelatin and enteric polymer comprise about 25% to about 50% of the enteric soft capsule shell by weight.
16. An oral pharmaceutical composition comprising an enteric soft capsule shell comprising gelatin and an enteric polymer;
wherein a weight ratio of enteric polymer to gelatin is 1:2.6; and
the shell encapsulates a fill comprising at least 70% by weight eicosapentaenoic free fatty acid (EPA).
17. The composition of claim 16 , wherein the composition comprises 70% by weight EPA free fatty acid.
18. The composition of claim 17 , wherein the composition comprises about 30% by weight DHA.
19. The composition of claim 16 , wherein the composition comprises a weight ratio of EPA to DHA of about 2.5:1 to about 3:1.