Eflornithine and sulindac, fixed dose combination formulation
Provided herein are fixed-dose combination formulations of a pharmaceutically effective amount of eflornithine together with a pharmaceutically effective amount of sulindac. Also provided are methods of use and of methods of manufacture of these formulations.
1. A method of producing a single dosage unit tablet comprising (a) about 375 mg of eflornithine hydrochloride monohydrate, (b) about 75 mg of sulindac, and (c) about 1 to about 1.5 weight percent magnesium stearate comprising:
(a) pre-mixing the sulindac and a first excipient to form a first mixture;
(b) mixing the first mixture with a second mixture comprising eflornithine hydrochloride monohydrate and a second excipient to form a blend;
(c) screening the blend to form a granulated blend;
(d) adding magnesium stearate to the granulated blend to obtain a final blend; and
(e) applying a compression force to the final blend to form the tablet.
2. The method of claim 1 , further comprising blending the granulated blend prior to step (d) and blending the final blend prior to step (e).
3. The method of claim 1 , wherein the first excipient is colloidal silicon dioxide.
4. The method of claim 1 , wherein the second excipient is silicified microcrystalline cellulose.
5. The method of claim 1 , wherein the pre-mixing step (a) is performed in a polyethylene-coated container.
6. The method of claim 1 , wherein the mixing step (b) is performed in a diffusion blender.
7. The method of claim 1 , wherein the magnesium stearate is sieved through a screen prior to step (d).
8. The method of claim 7 , wherein the screen is a 500 μm screen.
9. The method of claim 1 , wherein the screening step (c) comprises applying the blend to a rotative calibrator.
10. The method of claim 9 , wherein the rotative calibrator comprises a 1.0 mm screen.
11. The method of claim 1 , further comprising a pre-compression step after step (d) and prior to step (e), wherein the blend is compressed with a force lower than the force of step (e) to form a pre-compressed blend, further wherein the compression force of step (e) then acts on the pre-compressed blend to form the tablet.
12. The method of claim 11 , wherein the pre-compression step prevents tablet capping.
13. The method of claim 11 , wherein a compression force of the pre-compression step is applied at about 5 to about 15 percent of the compression force applied in step (e).
14. The method of claim 11 , wherein the compression force of the pre-compression step is from 2.5 to 3.5 kN.
15. The method of claim 14 , wherein the compression force of the pre-compression step is about 3 kN.
16. The method of claim 1 , wherein the compression force of step (e) is from 20 to kN.
17. The method of claim 16 , wherein the compression force of step (e) is about 25 kN.
18. The method of claim 1 , further comprising coating the tablet.
19. The method of claim 18 , wherein the coating comprises hydroxypropyl methylcellulose, titanium dioxide, polyethylene glycol, and iron oxide yellow.