US2003045503A1PendingUtilityA1

Composition for the relief of joint pain and myofascial pain and method of preparing same

Assignee: NATUROPATHIC LAB INTERNATIONALPriority: Dec 23, 1998Filed: Sep 30, 2002Published: Mar 6, 2003
Est. expiryDec 23, 2018(expired)· nominal 20-yr term from priority
A61K 47/44A61K 9/0014A61K 31/737A61K 31/726A61K 47/10A61K 31/045A61K 47/06
39
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Claims

Abstract

A stable, formulation comprising glucosamine and chondroitin compounds in a base which can be used for topical application to relieve joint pain and myofascial pain. A method of preparing the composition by adding the glucosamine and chondroitin after the rest of the components of the formulation have been mixed and heated is also disclosed.

Claims

exact text as granted — not AI-modified
I claim:  
     
         1 . A topical formulation comprising glucosamine and chondroitin in a substantially anhydrous base, wherein the formulation is stable for at least 10 days.  
     
     
         2 . The formulation of  claim 1 , wherein the glucosamine is present in the form of glucosamine sulfate.  
     
     
         3 . The formulation of  claim 1 , wherein the chondroitin is present in the form of chondroitin sulfate.  
     
     
         4 . The formulation of  claim 1 , wherein the base comprises anhydrous lanolin.  
     
     
         5 . The formulation of  claim 4 , wherein the base further comprises menthol.  
     
     
         6 . The formulation of  claim 1 , wherein the base comprises menthol.  
     
     
         7 . The formulation of  claim 1 , wherein the formulation is stable for at least 30 days.  
     
     
         8 . The formulation of  claim 1 , wherein the compound is stable for at least 60 days.  
     
     
         9 . The composition of  claim 1 , wherein the chondroitin and the glucosamine are each independently present in an amount from about 0.01% to about 3% by weight.  
     
     
         10 . The composition of  claim 9 , wherein the chondroitin and the glucosamine are each independently present in an amount about 0.05% to about 2% by weight.  
     
     
         11 . The composition of  claim 10 , wherein the chondroitin and the glucosamine are each independently present in an amount from about 0.1% to about 1.5% by weight.  
     
     
         12 . A process for preparing a substantially anhydrous topical formulation comprising a base, chondroitin, and glucosamine which is stable for at least 10 days, the process comprising the following steps: 
 (a) mixing the components of the base, and heating the base to a temperature from about 120° F. to about 160° F.;    (b) letting the base from step (a) stand for a period of at least two hours at a temperature of about 50° F. to about 90° F.;    (c) mixing the chondroitin and the glucosamine into the mixture from step (b).    
     
     
         13 . The process according to  claim 12 , wherein the mixture from step (c) is allowed to stand for a period of at least 1 hour, followed by additional mixing.  
     
     
         14 . The process according to  claim 12 , wherein the mixing of step (a) occurs at a temperature from about 130° to 150° F.  
     
     
         15 . The process according to  claim 14 , wherein the mixing of step (a) occurs at a temperature of about 140° F.  
     
     
         16 . The process according to  claim 12 , wherein step (b) occurs at a temperature from about 60° F. to about 80° F.  
     
     
         17 . The process according to  claim 12 , wherein, in step (b), the base from step (a) is allowed to stand for at least 8 hours.  
     
     
         18 . The process according to  claim 17 , wherein, in step (b), the base from step (a) is allowed to stand for at least 12 hours.  
     
     
         19 . The process according to  claim 13 , wherein the mixture from step (c) is allowed to stand for about 2 hours, followed by about 2 hours of additional mixing.  
     
     
         20 . A formulation for topical formulation comprising an analgesic, chondroitin, and glucosamine.  
     
     
         21 . The formulation of  claim 20 , wherein the analgesic is menthol.  
     
     
         22 . The formulation of  claim 21 , wherein the chondroitin is present in the form of chondroitin sulfate, and the glucosamine is present in the form of glucosamine sulfate.  
     
     
         23 . A method for treating joint pain or myofascial pain comprising the application of an effective amount of the composition of  claim 1  to areas of the skin overlying the painful joint or soft tissue.

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