US2013071443A1PendingUtilityA1

Glycosaminoglycans

Assignee: COOL SIMONPriority: Sep 16, 2011Filed: Sep 14, 2012Published: Mar 21, 2013
Est. expirySep 16, 2031(~5.1 yrs left)· nominal 20-yr term from priority
C08B 37/0078A61P 9/10A61L 2300/412A61K 31/737A61L 27/54A61L 27/34A61K 31/727A61K 38/1866
58
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Claims

Abstract

Heparan sulphate HS7 is disclosed, together with the use of HS7 in the growth and/or development and/or regeneration of tissue.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . Isolated or substantially purified heparan sulphate HS7, wherein following digestion with heparin lyases I, II and III and then subjecting the resulting disaccharide fragments to capillary electrophoresis analysis the heparan sulphate HS7 has a disaccharide composition comprising: 
       
         
           
                 
                 
                 
               
                     
                     
                 
                     
                   Disaccharide 
                   Normalised weight percentage 
                 
                     
                     
                 
                     
                   ΔUA,2S-GlcNS,6S 
                   11.08 ± 3.0 
                 
                     
                   ΔUA,2S-GlcNS 
                    4.46 ± 2.0 
                 
                     
                   ΔUA-GlcNS,6S 
                   15.84 ± 3.0 
                 
                     
                   ΔUA,2S-GlcNAc,6S 
                    4.76 ± 2.0 
                 
                     
                   ΔUA-GlcNS 
                   20.27 ± 3.0 
                 
                     
                   ΔUA,2S-GlcNAc 
                    1.01 ± 0.5 
                 
                     
                   ΔUA-GlcNAc,6S 
                   10.63 ± 3.0 
                 
                     
                   ΔUA-GlcNAc 
                   31.95 ± 3.0 
                 
                     
                     
                 
             
                
                
                
               
               
                
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         2 . Isolated or substantially purified heparan sulphate HS7 wherein following digestion with heparin lyases I, II and III and then subjecting the resulting disaccharide fragments to capillary electrophoresis analysis the heparan sulphate HS7 has a disaccharide composition comprising: 
       
         
           
                 
                 
                 
               
                     
                     
                 
                     
                   Disaccharide 
                   Normalised weight percentage 
                 
                     
                     
                 
                     
                   ΔUA,2S-GlcNS,6S 
                   11.08 ± 1.0 
                 
                     
                   ΔUA,2S-GlcNS 
                    4.46 ± 0.4 
                 
                     
                   ΔUA-GlcNS,6S 
                   15.84 ± 1.0 
                 
                     
                   ΔUA,2S-GlcNAc,6S 
                    4.76 ± 0.6 
                 
                     
                   ΔUA-GlcNS 
                   20.27 ± 3.0 
                 
                     
                   ΔUA,2S-GlcNAc 
                    1.01 ± 0.4 
                 
                     
                   ΔUA-GlcNAc,6S 
                   10.63 ± 1.0 
                 
                     
                   ΔUA-GlcNAc 
                   31.95 ± 1.6 
                 
                     
                     
                 
             
                
                
                
               
               
                
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         3 . HS7 according to  claim 1  wherein the HS7 is capable of binding SEQ ID NO:1 or 2. 
     
     
         4 . HS7 according to  claim 1  obtained by a method comprising:
 (i) providing a solid support having polypeptide molecules adhered to the support, wherein the polypeptide comprises a heparin-binding domain having the amino acid sequence of SEQ ID NO:1; 
 (ii) contacting the polypeptide molecules with a mixture comprising glycosaminoglycans such that polypeptide-glycosaminoglycan complexes are allowed to form; 
 (iii) partitioning polypeptide-glycosaminoglycan complexes from the remainder of the mixture; 
 (iv) dissociating glycosaminoglycans from the polypeptide-glycosaminoglycan complexes; and 
 (v) collecting the dissociated glycosaminoglycans. 
 
     
     
         5 . HS7 according to  claim 4  wherein the mixture comprising glycosaminoglycans is a heparan sulphate preparation obtained from porcine mucosa. 
     
     
         6 . A composition, pharmaceutical composition or medicament comprising HS7 according to  claim 1 . 
     
     
         7 . The composition, pharmaceutical composition or medicament of  claim 6  wherein the composition, pharmaceutical composition or medicament further comprises VEGF protein. 
     
     
         8 . A method of treating a disease, condition or injury to tissue in a patient, the method comprising administration of a therapeutically effective amount of HS7 according to  claim 1  to the patient, thereby treating a disease, condition or injury to tissue of the patient. 
     
     
         9 . The method of  claim 8  wherein the method involves the stimulation or promotion of the growth of blood vessels in the patient. 
     
     
         10 . The method of  claim 8  wherein the method comprises administering HS7 to tissue at or surrounding a wound or location on the patient's body at which blood vessel growth is required. 
     
     
         11 . The method of  claim 8  wherein the method further comprises administering VEGF protein to the patient. 
     
     
         12 . A method of treating a disease, condition or injury to tissue in a patient, the method comprising surgically implanting a biocompatible implant or prosthesis, which implant or prosthesis comprises a biomaterial and HS7 according to  claim 1 , into tissue of the patient at or surrounding the site of the disease, condition or injury. 
     
     
         13 . A biocompatible implant or prosthesis comprising a biomaterial and isolated or substantially purified HS7 according to  claim 1 . 
     
     
         14 . The implant or prosthesis of  claim 13  wherein the implant or prosthesis is coated with said HS7. 
     
     
         15 . The implant or prosthesis of  claim 13  wherein the implant or prosthesis is impregnated with said HS7. 
     
     
         16 . A method of forming a biocompatible implant or prosthesis, the method comprising the step of coating or impregnating a biomaterial with isolated or substantially purified HS7 according to  claim 1 . 
     
     
         17 . A method of promoting growth of blood vessels, the method comprising administering isolated or substantially purified HS7 according to  claim 1  to vascular cells or to vascular tissue. 
     
     
         18 . The method of  claim 17  wherein the vascular cells or vascular tissue are contacted with HS7 in vitro. 
     
     
         19 . The method of  claim 17  wherein the vascular cells or vascular tissue are contacted with HS7 in vivo.

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