Ex Parte Rouns et al - Page 7


               Appeal No. 2006-0817                                                                                                  
               Application 10/325,443                                                                                                

               formula “would correspond to the amine monomers of the acrylates of the type taught in Michal                         
               (2-aminoethyl methacrylate),” which when “treated with an acid the amine group would be                               
               protonated and thus form the neutralized salt thereof” in “[a]cid body fluids,” resulting in “the                     
               quaternary amine structure” (answer, pages 4-5).  In response to appellants’ arguments (brief,                        
               page 7), the examiner contends that “[t]here will always be some degree of protonation” (answer,                      
               page 7).                                                                                                              
                       The sole applicable disclosure of “2-aminoethyl methacrylate” in Michal ‘285 is with                          
               respect to the embodiment at col. 7, l. 57, to col. 8, l. 13, particularly, col. 8, l. 2.  In this                    
               disclosure, the material is described as “a (co)monomer” for a hydrophilic agent top coat.                            
               However, this is in the context of “the binding component comprises an aldehyde compound and                          
               the top coat is a compound having amine groups” (col. 7, ll. 57-59).  We find that one of                             
               ordinary skill in this art would have recognized from this embodiment that the reaction of the                        
               amine and aldehyde functional groups would result in imine moieties, as is well known in the                          
               organic chemistry arts, 2 which moieties in the disclosure of Michal ‘285 crosslink the binding                       
               component and the polymeric top coat (see also col. 6, l. 65, to col. 7, l. 3).                                       
                       Thus, even if a number of amino groups remain unreacted in the polymeric top coat and                         
               may be protonated as the examiner finds, there is no showing on this record that the same would                       
               result in a hydrogel polymer and certainly not a hydrogel quaternary amine acrylate polymer,                          
               particularly one having more than 50,000 repeating units, as the examiner contends.                                   
                       Accordingly, in the absence of a prima facie case of obviousness, we reverse the ground                       
               of rejection of appealed claims 2 through 4 and 6 through 35 under 35 U.S.C. § 103(a) over the                        
               Michal references.                                                                                                    
                       The examiner’s decision is affirmed.                                                                          
                       No time period for taking any subsequent action in connection with this appeal may be                         
               extended under 37 CFR § 1.136(a)(1)(iv) (2005).                                                                       
                                                            AFFIRMED                                                                 

                                                                                                                                    
               2  See, e.g., Romeo B. Wagner and Harry D. Zook, “Imines,” “Method 465. Condensation of                               
               Carbonyl Compounds with Amines,” Synthetic Organic Chemistry 728 (New York. John Wiley                                
               & Sons, Inc. 1953) (copy not provided).                                                                               

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