Claims for Patent: 9,180,096
✉ Email this page to a colleague
Summary for Patent: 9,180,096
Title: | Formulation of diclofenac |
Abstract: | The present invention relates to methods for producing particles of diclofenac using dry milling processes as well as compositions comprising diclofenac, medicaments produced using diclofenac in particulate form and/or compositions, and to methods of treatment of an animal, including man, using a therapeutically effective amount of diclofenac administered by way of said medicaments. |
Inventor(s): | Dodd; Aaron (Centennial Park, AU), Meiser; Felix (Mount Claremont, AU), Norret; Marck (Darlington, AU), Russell; Adrian (Rivervale, AU), Bosch; H William (Bryn Mawr, PA) |
Assignee: | iCeutica Pty Ltd. (Philadelphia, PA) |
Application Number: | 14/621,269 |
Patent Litigation and PTAB cases: | See patent lawsuits and PTAB cases for patent 9,180,096 |
Patent Claims: |
1. A solid oral unit dose of a pharmaceutical composition containing 18 mg of diclofenac acid, wherein the D(90) of the diclofenac acid, on a particle volume basis, is
less than 5000 nm, and wherein the unit dose, when tested in vitro by USP Apparatus I (Basket) method of U.S. Pharmacopoeia at 100 rpm at 37.degree. C. in 900 ml of 0.05% sodium lauryl sulfate in citric acid solution buffered to pH 5.75, has a
dissolution rate of diclofenac acid such that 94%, by weight, is released by 75 minutes.
2. The unit dose of claim 1, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 3000 nm. 3. The unit dose of claim 2, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 60 minutes. 4. The unit dose of claim 2, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 45 minutes. 5. The unit dose of claim 2, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 30 minutes. 6. The unit dose of claim 1, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 2000 nm. 7. The unit dose of claim 6, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 60 minutes. 8. The unit dose of claim 6, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 45 minutes. 9. The unit dose of claim 6, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 30 minutes. 10. The unit dose of claim 1, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 1900 nm. 11. The unit dose of claim 1, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 1800 nm. 12. The unit dose of claim 1, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 60 minutes. 13. The unit dose of claim 1, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 45 minutes. 14. The unit dose of claim 1, wherein the unit dose has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 30 minutes. 15. The unit dose of claim 1, wherein a single dose provides perceptible pain relief to a patient suffering from acute pain. 16. A solid oral unit dose of a pharmaceutical composition containing 35 mg of diclofenac acid, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 5000 nm, and wherein the unit dose, when tested in vitro by USP Apparatus I (Basket) method of U.S. Pharmacopoeia at 100 rpm at 37.degree. C. in 900 ml of 0.05% sodium lauryl sulfate in citric acid solution buffered to pH 5.75, has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 75 minutes. 17. The unit dose of claim 16, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 3000 nm. 18. The unit dose of claim 17, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 60 minutes. 19. The unit dose of claim 17, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 45 minutes. 20. The unit dose of claim 17, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 30 minutes. 21. The unit dose of claim 16, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 2000 nm. 22. The unit dose of claim 21, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 60 minutes. 23. The unit dose of claim 21, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 45 minutes. 24. The unit dose of claim 21, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 30 minutes. 25. The unit dose of claim 16, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 1900 nm. 26. The unit dose of claim 16, wherein the D(90) of the diclofenac acid, on a particle volume basis, is less than 1800 nm. 27. The unit dose of claim 16, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 60 minutes. 28. The unit dose of claim 16, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 45 minutes. 29. The unit dose of claim 16, wherein the unit dose has a dissolution rate of diclofenac acid such that 95%, by weight, is released by 30 minutes. 30. The unit dose of claim 16, wherein a single dose provides perceptible pain relief to a patient suffering from acute pain. |