Pharmaceutical formulation
Disclosed are aqueous pharmaceutical compositions which provide sustained released delivery of corticosteroid compounds. The pharmaceutical composition comprises a soluble corticosteroid and at least one viscosity enhancing agent. Also provided are methods for using the pharmaceutical compositions in an epidural injection, intra-articular injection, or an intra-lesional injection.
1. A method for treating inflammation and/or pain in an individual in need thereof, comprising:
injecting an aqueous pharmaceutical composition into the epidural space of the individual, wherein the aqueous pharmaceutical composition comprises:
a soluble corticosteroid selected from the group consisting of soluble salts and esters of dexamethasone, and
at least one viscosity enhancing agent,
wherein the at least one viscosity enhancing agent is sodium hyaluronate or hyaluronic acid, the molecular weight of the at least one viscosity enhancing agent is between 1.0 MDa and 2.5 MDa, and the concentration of the at least one viscosity enhancing agent is between 1.0% w/v and 1.5% w/v;
and wherein the aqueous pharmaceutical composition is substantially free of insoluble corticosteroids.
2. The method of claim 1 , wherein the soluble corticosteroid is dexamethasone sodium phosphate.
3. The method of claim 1 , wherein the at least one viscosity enhancing agent is hyaluronic acid.
4. The method of claim 1 , wherein the at least one viscosity enhancing agent is sodium hyaluronate.
5. The method of claim 1 , wherein the molecular weight of the at least one viscosity enhancing agent is between 1.0 MDa and 2.0 MDa.
6. The method of claim 1 , wherein the molecular weight of the at least one viscosity enhancing agent is between 1.2 MDa and 1.8 MDa.
7. The method of claim 1 , wherein the soluble corticosteroid is dexamethasone sodium phosphate and the at least one viscosity enhancing agent is sodium hyaluronate,
wherein the molecular weight of the sodium hyaluronate is between 1.0 MDa and 2.0 MDa, and the concentration of the sodium hyaluronate is about 1.25% w/v.
8. The method of claim 7 , wherein the aqueous pharmaceutical composition comprises dexamethasone sodium phosphate at a concentration of about 6.58 mg/mL.
9. The method of claim 1 , wherein the aqueous pharmaceutical composition comprises a soluble salt or ester of dexamethasone present at a weight equivalent to achieve a dexamethasone concentration of about 5 mg/mL.
10. The method of claim 1 , wherein less than 27 N of force is used to inject the aqueous pharmaceutical composition into the epidural space.
11. The method of claim 1 , wherein the aqueous pharmaceutical composition further comprises a preservative and/or an anesthetic.
12. The method of claim 1 , wherein the individual has one or more of lower back pain, spinal stenosis, disc herniation, radiculitis or chronic discogenic pain.
13. The method of claim 1 , wherein the individual has chronic discogenic pain.
14. The method of claim 1 , wherein the individual has spondylolysis.
15. The method of claim 1 , wherein the individual is injected with the aqueous pharmaceutical composition once every 1 to 12 weeks.
16. The method of claim 1 , wherein the injecting is via an interlaminar injection.
17. The method of claim 1 , wherein the injecting is via a caudal injection.
18. The method of claim 1 , the injecting is via a transforaminal injection.
19. The method of claim 1 , wherein the aqueous pharmaceutical composition has a viscosity of between 1 kcP and 10 kcP.
20. The method of claim 1 , wherein the aqueous pharmaceutical composition has a viscosity of between 1 kcP and 5 kcP.