초록 ▼

The instant invention is directed toward a dermal delivery system composition comprising an aqueous base vehicle including American Emu oil, Isopropyl Palmitate (PROTACHEM IPP), PEG-8 (a polyethylene glycol available under the tradename PROTACHEM 400), methylsulfonylmethane (MSM) and SEPIGEL 305 (a

The instant invention is directed toward a dermal delivery system composition comprising an aqueous base vehicle including American Emu oil, Isopropyl Palmitate (PROTACHEM IPP), PEG-8 (a polyethylene glycol available under the tradename PROTACHEM 400), methylsulfonylmethane (MSM) and SEPIGEL 305 (a combination including polyacrylamide/C13-C14 Iso-paraffin and Laureth-7), in combination with an analgesic composition, such as ibuprofen, and to processes for the manufacture and use thereof.

대표청구항 ▼

What is claimed is: 1. An alcohol-free analgesic composition effective for transdermal delivery consisting essentially of: about 3% Emu Oil, about 3% Isopropyl Palmitate, about 4% PEG-8, about 0.75% methylsulfonylmethane, and a gelling agent including a combination of about 40% polyacrylamide, abou

What is claimed is: 1. An alcohol-free analgesic composition effective for transdermal delivery consisting essentially of: about 3% Emu Oil, about 3% Isopropyl Palmitate, about 4% PEG-8, about 0.75% methylsulfonylmethane, and a gelling agent including a combination of about 40% polyacrylamide, about 15% C13-C14 Iso-paraffin, about 5% Laureth-7 and sterile water sufficient to make 100% in an amount effective for gelling, about 10% of an analgesic composition, and sterile water sufficient to make 100%. 2. A composition for treating the discomfort of pain and/or inflammation in a patient comprising: about 3% Emu Oil, about 3% Isopropyl Palmitate, about 4% PEG-8, about 0.75% methylsulfonylmethane, and a gelling agent including a combination of about 40% polyacrylamide, about 15% C13-C14 Iso-paraffin, about 5% Laureth-7 and sterile water sufficient to make 100% in an amount effective for gelling, about 10% of an analgesic composition, and sterile water sufficient to make 100%. 3. A process for treating the discomfort of pain and/or inflammation and pain in a patient comprising: identifying a location of pain and/or inflammation in a patient; identifying a location or trigger points associated with pain/or inflammation in a patient; transdermally delivering to at least one location of trigger point said points an analgesic composition consisting essentially of about 3% Emu oil, 3% Isopropyl Palmitate and about 4% PEG-8, about 0.75% methylsulfonylmethane, a gelling agent including a combination of about 40% polyacrylamide, about 15% C13-C14 Iso-paraffin, about 5% Laureth-7 and sterile water sufficient to make 100% in an amount effective for gelling, about 10% of an analgesic composition, and sterile water sufficient to make 100%; whereby the discomfort of said pain and/or inflammation is treated. 4. A process for manufacturing an alcohol-free analgesic composition effective for transdermal delivery comprising: providing said analgesic composition; providing about 3% Emu oil in a high speed mixing apparatus; adding said analgesic composition to said Emu oil and mixing until a homogeneously blended composition is formed; adding about 3% Isopropyl Palmitate and about 4% PEG-8 to said homogeneously blend, and mixing for approximately 30 minutes; adding sterile water and mixing for approximately 5 minutes, to homogeneity; adding about 3% of a gelling agent including a combination of about 40% polyacrylamide, about 15% C13-C14 Iso-paraffin, about 5% Laureth-7 and sterile water sufficient to make 100%, and blending to achieve homogeneity and a gel-like consistency; and adding additional said gelling agent in 1% increments, if necessary, until desired gel consistency is achieved. 5. The product produced by the process of claim 4. 6. An alcohol-free transdermal delivery system consisting essentially of: about 3% Emu oil, about 3% Isopropyl Palmitate, about 4% PEG-8, about 0.75% methylsulfonylmethane, a gelling agent including a combination of about 40% polyacrylamide, about 15% C13-C14 Iso-paraffin, about 5% Laureth-7 and sterile water sufficient to make 100% in an amount effective for gelling, and sterile water sufficient to make 100%.