ANTI-INFLAMMATORY DRUG-CANNABINOID-COMPRISING NANOEMULSIONS AND METHODS OF USING THE SAME
The disclosed formulations include Diclofenac Sodium Salt and at least one cannabinoid. Other formulations include other anti-inflammatory drugs such as methotrexate and prednisone, for example. In addition, methods of using formulations to treat diseases or disorders such as arthritis, pain, inflammation and fever are disclosed.
1 . A pharmaceutical formulation comprising cannabinoids, or a salt or derivative thereof, formulated in a nanoemulsion comprising droplets having an average particle size of less than about 1 micron, wherein the cannabinoids are present in the formulation at a concentration of about 0.01 to about 15.0% (w/w).
2 . A pharmaceutical formulation according to claim 1 , wherein the formulation further comprises diclofenac sodium, or a salt or derivative thereof, wherein the diclofenac sodium, or a salt or derivative thereof, is present in the formulation at a concentration of about 1% to about 5% (w/w).
3 . A pharmaceutical formulation comprising diclofenac sodium, or a salt or derivative thereof, formulated in a nanoemulsion comprising droplets having an average particle size of less than about 1 micron, wherein the diclofenac sodium, or a salt or derivative thereof, is present in the formulation at a concentration of about 1% to about 5% (w/w).
4 . A pharmaceutical formulation according to claim 3 , wherein the formulation further comprises water at a concentration of about 35 to 38% and a pharmaceutically acceptable oil at a concentration of about 35 to 38%, and further wherein the pH range of the formulation is 7 to 8.3.
5 . A pharmaceutical formulation according to claim 1 , wherein the formulation further comprises methotrexate, which is present in the formulation at a concentration of about 0.5% to about 1.0% (w/w).
6 . A pharmaceutical formulation according to claim 1 , wherein the formulation further comprises prednisone, which is present in the formulation at a concentration of about 0.1% to about 1.0% (w/w).
7 . A pharmaceutical formulation according to claim 6 , wherein the prednisone has a concentration of 0.1%, and the formulation further comprises 4 to 10% of a pharmaceutically acceptable oil, 0.2 to 0.3% ethanol, 90 to 95% water, and wherein the formulation has a pH range of 7.0 to 8.
8 . A pharmaceutical formulation according to claim 6 , wherein the prednisone has a concentration of 1.0%, and the formulation further comprises 33 to 40% of a pharmaceutically acceptable oil, 37.2 to 47% water, and wherein the formulation has a pH range of 7.8 to 8.4.
9 . A pharmaceutical formulation according to claim 1 , further comprising 0.1% diclofenac sodium, 4 to 10% of a pharmaceutically acceptable oil, 0.2 to 0.3% ethanol, wherein the pH of the formulation is 7 to 8.0.
10 . A pharmaceutical formulation according to claim 1 , wherein the cannabinoids are present in the formulation at a concentration of 1 to 10%, and wherein the formulation further comprises 0.5 to 1.0% methotrexate, 1 to 5% diclofenac sodium, water ranging from 35 to 42%, and a pharmaceutically acceptable oil ranging from 37% to 63%, wherein the pH of the formulation is in the range of 7.0 to 8.2.
11 . A pharmaceutical formulation according to claim 1 , wherein the nanoemulsion comprises a pharmaceutically acceptable oil having at least one oxidizable metal of less than one part per million in said oil, wherein the at least one oxidizable metal is one or more of copper, chromium, lithium, and molybdenum.
12 . A pharmaceutical formulation according to claim 1 , wherein the cannabinoids are present in the formulation at a concentration of about 1 to about 5% (w/w), and wherein the formulation further comprises diclofenac sodium, or a salt or derivative thereof, present in the formulation at a concentration of about 0.5% to about 2% (w/w), about 10% to about 90% (w/w) water, about 10 to about 60% (w/w) of a pharmaceutically acceptable oil, about 1 to about 15% of a surfactant, and about 0.05 to about 0.5% (w/w) of an organic solvent.
13 . A pharmaceutical formulation according to claim 1 , wherein the cannabinoids are present in the formulation at a concentration of about 0.01 to about 0.5% (w/w), and wherein the formulation further comprises diclofenac sodium, or a salt or derivative thereof, present in the formulation at a concentration of about 0.01% to about 2% (w/w), about 10% to about 90% (w/w) water, about 10 to about 60% (w/w) of a pharmaceutically acceptable oil, about 1 to about 15% of a surfactant, and about 0.05 to about 0.5% (w/w) of an organic solvent.
14 . A pharmaceutical formulation according to claim 1 , wherein the cannabinoids comprise about 0.01 to about 0.5% (w/w) tetrahydrocannabinol (THC), or a salt or derivative thereof, and about 0.01 to about 15% (w/w) cannabidiol (CBD) or CBD isolate (CBDi), or a salt or derivative thereof, wherein the formulation further comprises about 10 to about 90% (w/w) water, about 10 to about 60% (w/w) of a pharmaceutically acceptable oil, about 1 to about 15% (w/w) of a surfactant, and about 0.05 to about 0.5% (w/w) of an organic solvent.
15 . A pharmaceutical formulation comprising cannabinoids, or a salt or derivative thereof, formulated in a nanoemulsion comprising droplets having an average particle size of less than about 1 micron, wherein the cannabinoids are present in the formulation at a concentration of 0.01% to 75.0% (w/w) of the formulation, and wherein the formulation further comprises a pharmaceutically acceptable oil having an oxidizable metal of less than one part per million.
16 . A pharmaceutical formulation according to claim 15 , wherein the formulation further comprises an anti-inflammatory, and the anti-inflammatory is one or more of prednisone and diclofenac sodium, or a salt or derivative thereof.
17 . A pharmaceutical formulation according to claim 15 , wherein the formulation further comprises methotrexate.
18 . A pharmaceutical formulation according to claim 16 , wherein the formulation further comprises methotrexate.
19 . A method of treating arthritis conditions in a subject suffering joint pain, comprising topically administering a pharmaceutical formulation of claim 1 on the skin of a subject requiring such treatment.
20 . The method of claim 19 , wherein the pharmaceutical formulation further comprises an anti-inflammatory, and said anti-inflammatory is one or more of prednisone and diclofenac sodium, or a salt or derivative thereof.