Sustained release formulation of nalbuphine
View Patent ↗Sustained release formulations of nalbuphine or pharmaceutically acceptable salts thereof; methods for making the sustained release formulations of nalbuphine or pharmaceutically acceptable salts thereof; and methods for using the sustained release formulations of nalbuphine or pharmaceutically acceptable salts thereof to treat patients suffering from pain are provided.
1. A sustained release oral solid dosage form comprising nalbuphine or a pharmaceutically acceptable salt thereof in a gel matrix sustained release delivery system, wherein the dosage form providing an onset of nalbuphine effect from about 30 minutes of dosing to within about 6 hours of dosing and a controlled release of the nalbuphine over a time period of at least about 8 hours, in the form of a tablet.
2. The dosage form of claim 1 , which provides a C max from about 1.95 to about 102.00 ng/ml in a healthy human subject.
3. The dosage form of claim 1 , which provides a Tmax at about 1.00 hour to about 16 hours after administration of the dosage form to a healthy human subject.
4. The dosage form of claim 1 , wherein the median T max ranges from about 1.5 to about 8.0 hours after administration of the dosage form to healthy human subjects.
5. The dosage form of claim 1 , wherein the sustained release delivery system comprises at least one hydrophilic compound in an amount from about 5% to about 80% by weight.
6. The dosage form of claim 1 , which is in the form of a tablet, wherein the sustained release delivery system comprises at least one hydrophilic compound in an amount from about 5% to about 80% by weight and at least one pharmaceutical diluent.
7. The dosage form of claim 1 , wherein the sustained release delivery system comprises a compound selected from gums, cellulose ethers, acrylic resins, polyvinyl pyrrolidone, protein-derived compounds, and mixtures thereof.
8. The dosage form of claim 1 , wherein the gel matrix comprises a gum selected from xanthan, tragacanth, pectins, acacia, karaya, alginates, agar, guar, hydroxypropyl guar, carrageenan, locust bean gums, gellan gums, hydroxyalkyl celluloses, carboxyalkyl celluloses, and mixtures thereof.
9. The dosage form of claim 1 , which comprises from about 1 mg to about 200 mg nalbuphine hydrochloride.
10. The dosage form of claim 9 , wherein the sustained release delivery system comprises about 10 mg to about 420 mg.
11. The dosage form of claim 1 , which provides a mean C max from about 4.130 to about 32.17 ng/ml in healthy human subjects.
12. The dosage form of claim 1 , wherein the median T max ranges from about 1.5 to about 8.0 hours after administration of the dosage form to healthy human subjects.
13. A sustained release oral tablet comprising nalbuphine or a pharmaceutically acceptable salt thereof homogeneously dispersed in a sustained release delivery system selected from the group consisting of gums, cellulose ethers, acrylic resins, polyvinyl pyrrolidone, protein-derived compounds, and mixtures thereof, and at least one pharmaceutical diluent, the tablet providing an onset of nalbuphine effect from about 30 minutes of dosing to within about 6 hours of dosing and a release of the nalbuphine over a time period of at least about 8 hours.
14. The sustained release oral tablet of claim 1 , comprising a sustained release film including a release-modifying compound.
15. The sustained release oral tablet of claim 1 , wherein the dosage form maintains a plateau of a relatively constant blood serum level of nalbuphine during a dosage interval of about 1 hours to about 12 hours.
16. The sustained release oral tablet of claim 15 , wherein the plateau has a duration of about 2 to about 10 hours.
17. The sustained release oral tablet of claim 15 , wherein the plateau has a duration of about 6 hours to about 9 hours.
18. The sustained release oral tablet of claim 15 , wherein the dosage form provides a minimum blood serum level of nalbuphine observed during the plateau that is not more than 25% below the mean blood serum level for all time points in the plateau.
19. The sustained release oral tablet of claim 15 , wherein the minimum blood serum level is not more than 20% below the mean blood serum level for all time points in the plateau.
20. The sustained release oral tablet of claim 1 , further comprising an enteric coating or a hydrophilic coating.
21. The sustained release oral tablet of claim 1 , wherein the sustained release delivery system comprises a hydrophilic compound that forms a gel matrix.
22. A sustained release oral tablet, comprising from about 1 mg to about 200 mg nalbuphine or a pharmaceutically acceptable salt thereof in a sustained release matrix delivery system, the tablet providing an onset of nalbuphine effect from about 30 minutes of dosing to within about 6 hours of dosing and a duration of nalbuphine effect of at least 8 hours.
23. The dosage form of claim 22 , which provides a C max from about 1.95 to about 102.00 ng/ml in a healthy human subject.
24. The dosage form of claim 23 , which provides a Tmax at about 1.00 hour to about 16 hours after administration of the dosage form to a healthy human subject.