US2004224906A1PendingUtilityA1

Process for extracting polyphenolic antioxidants from purine-containing plants

Priority: Feb 2, 1999Filed: Jun 7, 2004Published: Nov 11, 2004
Est. expiryFeb 2, 2019(expired)· nominal 20-yr term from priority
C07D 311/62A61Q 19/00A23G 1/30A23G 1/48A61K 8/9789A23G 3/36A23L 33/105A61K 2800/522A23G 9/42A23G 9/32A61K 36/00A23G 3/48A61K 36/5777A61K 36/742A23B 2/746A23B 2/733
47
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Claims

Abstract

Water soluble antioxidant composition derived from natural sources having less than 10 ppm chlorinated hydrocarbons, less than 0.5% by weight fat, at least 15% by weight in total polyphenolic antioxidants, less than 5% by weight purine components, less than 0.5% by weight caffeine, and a Trolox Equivalent Antioxidant Capacity value of at least 0.4. The composition is suitable for use in pharmaceuticals, cosmetic, and nutritional compositions.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A process for isolating polyphenolic antioxidants from purine-containing plant material, comprising: 
 (a) extracting the plant material with a hydroxylic extracting liquid;    (b) selectively adsorbing the extract obtained in step (a) on a solid adsorbent which has a high polyphenol/purine adsorption selectivity; and    (c) desorbing the adsorbed material with a hydroxylic desorbing liquid.    
     
     
         2 . A process according to  claim 1 , in which the desorbed material is concentrated and optionally dried.  
     
     
         3 . A process according to  claim 1 , in which the adsorbent comprises polyvinylpolypyrrolidone or a chemical or physical modification thereof.  
     
     
         4 . A process according to any one of the preceding claims, in which the adsorbent comprises chitosan or a chemical or physical modification thereof.  
     
     
         5 . A process according to any one of the preceding claims, in which step (a) is carried out at a temperature below 50° C., preferably between 0 and 30° C.  
     
     
         6 . A process according to any one of the preceding claims, in which step (b) is carried out at a temperature below 30° C.  
     
     
         7 . A process according to any one of the preceding claims, in which step (c) is carried out at a temperature above 30° C., preferably between 50 and 110° C.  
     
     
         8 . A process according to any one of the preceding claims, in which the hydroxylic extracting liquid in step (a) comprises water.  
     
     
         9 . A process according to any one of the preceding claims, in which the hydroxylic desorbing liquid in step (c) comprises water and a lower alcohol or water and a lower ketone.  
     
     
         10 . A process according to any one of the preceding claims, in which said purine-containing plant material is cocoa, coffee or tea, especially cocoa.  
     
     
         11 . A water-soluble antioxidant composition obtainable using the process of any one of claims  1 - 10 , which is free of chlorinated hydrocarbons and substantially fat-free, and which contains at least 15% by weight in total of catechin, epicatechin and/or chlorogenic acid, less than 5% by weight of purine components, less than 0.5% by weight of caffeine and has a TEAC value of at least 0.4.  
     
     
         12 . A composition according to  claim 11 , which contains at least 20% by weight in total of catechin and epicatechin, and/or has a TEAC value of at least 0.6.  
     
     
         13 . A composition according to  claim 11  or  12 , which contains at least 25% by weight in total of catechin and epicatechin and/or less than 0.4% by weight of caffeine and/or less than 3% by weight of theobromine, and/or has a TEAC value of at least 0.8.  
     
     
         14 . A nutritional, pharmaceutical or cosmetic composition containing an antioxidant composition according to any one of claims  11 - 13 .  
     
     
         15 . A water soluble antioxidant composition derived from natural sources, comprising: 
 less than 10 ppm chlorinated hydrocarbons;    less than 0.5% by weight fat;    at least 15% by weight in total polyphenolic antioxidants;    less than 5% by weight of purine components;    less than 0.5% by weight caffeine; and    a Trolox Equivalent Antioxidant Capacity value of at least 0.4.    
     
     
         16 . The composition according to  claim 15 , comprising: at least 20% by weight in total of polyphenolic antioxidants; and 
 a Trolox Equivalent Antioxidant Capacity value of at least 0.6.    
     
     
         17 . The composition according to  claim 16 , comprising: 
 at least 25% by weight in total of polyphenolic antioxidants;    less than 0.4% by weight of caffeine; and    a Trolox Equivalent Antioxidant Capacity value of at least 0.8.    
     
     
         18 . The composition according to  claim 15 , comprising: 
 less than 1 ppm chlorinated hydrocarbons.    
     
     
         19 . The composition according to  claim 15 , comprising: less than 0.5 ppm chlorinated hydrocarbons.  
     
     
         20 . The composition according to  claim 15 , wherein the natural source is cocoa and the polyphenolic antioxidants comprise catechin, epicatechin.  
     
     
         21 . The composition according to  claim 15 , wherein the natural source is coffee and the polyphenolic antioxidants comprise catechin, epicatechin, chorogenic acids, and isomers of chorogenic acids .  
     
     
         22 . The composition according to  claim 16 , comprising less than 3.5% by weight of purine components.  
     
     
         23 . The composition according to  claim 15 , comprising a Trolox Equivalent Antioxidant Capacity value about 1.5.  
     
     
         24 . The composition according to  claim 15 , wherein the composition is used as an ingredient for nutritional products.  
     
     
         25 . The composition according to  claim 15 , wherein the composition is used as a basic substance for at least one of chocolate bars, beverages, confectionary, ice-cream, and pastries.  
     
     
         26 . The composition according to  claim 15 , wherein the composition is used in at least one of medicinal, nutraceutical, pharmaceutical, and cosmetic formulations.

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