US2004180081A1PendingUtilityA1

Compositions and kits for the removal of irritating compounds from bodily surfaces

Priority: Sep 5, 2002Filed: Mar 26, 2004Published: Sep 16, 2004
Est. expirySep 5, 2022(expired)· nominal 20-yr term from priority
A61P 25/02A61P 31/00A61P 29/00A61P 23/00A61P 23/02A61P 17/00A61K 31/165A61Q 17/00A61K 8/33A61K 8/42A61K 9/7084A61K 2800/88A61K 9/0014A61K 8/44A61K 8/86A61Q 19/10A61K 2800/75A61K 8/8152A61K 31/16
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Claims

Abstract

The invention provides compositions, methods and kits for the removal of harmful or irritating substances from bodily surfaces. Kits may include a composition containing capsaicin and a capsaicin-cleansing composition, e.g., a composition in which capsaicin is soluble.

Claims

exact text as granted — not AI-modified
1 . A method for treating an individual in need of treatment for a capsaicin-responsive condition comprising 
 (a) applying a first composition comprising capsaicin or a capsaicin analog to a bodily surface;    (b) applying a second composition in which capsaicin has a solubility of at least about 10% w/w to the bodily surface; and    (c) removing the second composition from the bodily surface.    
     
     
         2 . The method of  claim 1  further comprising administering an anesthetic to the individual prior to or simultaneously with the application of the first composition.  
     
     
         3 . The method of  claim 2  wherein the anesthetic is contained in a lotion or gel.  
     
     
         4 . The method of  claim 1  wherein the first composition is applied by affixing a skin-adherent patch containing the first composition to the bodily surface.  
     
     
         5 . The method of  claim 4  further comprising administering an anesthetic to the individual prior to or simultaneously with the application of the skin-adherent patch.  
     
     
         6 . The method of  claim 4  wherein the skin-adherent patch contains from about 5% to about 10% capsaicin.  
     
     
         7 . The method of  claim 1  wherein capsaicin has a solubility of at least about 20% (w/w) in the second composition.  
     
     
         8 . The method of  claim 1  wherein the second composition comprises at least 60% (w/w) polyethylene glycol.  
     
     
         9 . The method of  claim 1  wherein the capsaicin-responsive condition is selected from the group consisting of neuropathic pain, pain produced by mixed nociceptive and/or neuropathic mixed etiologies, inflammatory hyperalgesia, dermatitis, pruritis, itch, psoriasis, warts, headaches, wrinkles and skin cancer.  
     
     
         10 . A method for cleansing a bodily surface that has been contacted with capsaicin or a capsaicin analog comprising: 
 a) applying to the bodily surface a composition in which capsaicin has a solubility of at least about 10% w/w; and    b) removing said composition from the bodily surface.    
     
     
         11 . The method of  claim 10  wherein the substance is capsaicin.  
     
     
         12 . The method of  claim 10  wherein capsaicin has a solubility of at least about 20% w/w in the composition.  
     
     
         13 . The method of  claim 10  wherein the composition comprises about 60 to about 99 percent w/w polyethylene glycol.  
     
     
         14 . The method of  claim 13  wherein the composition further contains about 0.1 to about 4 percent w/w thickening agent, and the balance water.  
     
     
         15 . The method of  claim 13  wherein the composition contains about 80 to about 99 percent w/w polyethylene glycol.  
     
     
         16 . The method of  claim 15  wherein the composition further contains about 0.1 to about 2 percent w/w polyacrylate thickening agent and the balance water.  
     
     
         17 . The method of  claim 13  wherein the composition contains about 87 to about 91 percent w/w polyethylene glycol.  
     
     
         18 . The method of  claim 17  wherein the composition further contains about 0.3 to about 1.5 percent w/w polyacrylate thickening agent and the balance water.  
     
     
         19 . The method of  claim 18  wherein the composition is at a pH of about 7.0 to about 7.7.  
     
     
         20 . The method of  claim 19  wherein the composition further contains about 0.01 to about 0.03 percent w/w butylated hydroxyanisole, about 0.02 to about 0.2 percent w/w EDTA/EDTA salts, and the balance water.

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