Direct Determination of Blood Ammonia by Berthelot’s Coloraiton of Protein-free Supernatant Obtained by Folin-Wu Deproteinizaion
        The bulletin of the Yamaguchi Medical School Volume 15 Issue 3
        Page 207-217
        
    published_at 1968-09
            Title
        
        Direct Determination of Blood Ammonia by Berthelot’s Coloraiton of Protein-free Supernatant Obtained by Folin-Wu Deproteinizaion
        
        
    
                
                    Creators
                
                    Kitajima Kazuhiko
                
                
            
            
                
                    Creators
                
                    Miyamura Sigenori
                
                
            
            
                
                    Creators
                
                    Murakawa Setsuko
                
                
            
    
        
            Source Identifiers
        
    
         A direct determination of blood ammonia circumventing the use of microdiffusion apparatus which was devised by Fujii consists in (1) deproteinization of blood by a modified Folin-Wu's procedure, (2) coloration of thus deproteinized supernatant of blood by the Berthelot reaction and (3) colorimetry. This is a simple and convenient method, but our experience disclosed several drawbacks in it. A series of experiments were carried out in our laboratory in the hope that Fujii's method might be improved. The following is the outline of our improvement.  1゜. Collection of blood sample. Blood (about 3 ml) is withdrawn with a syringe by venous puncture, transferred into a test tube containing the crystals of potassium oxalate, stirred gently to prevent coagulation, and immediately  cooled by inserting into a pile of ice cubes so that release of ammonia from non-NH_3 nitrogen substances may be stopped completely.  2゜. Deproteinization. To the blood (1.0 ml) thus collected are added 10 g/dl sodium tungstate solution (0.5 ml) and 1 N sulfuric acid (0.5 ml), allowed to  stand (for 15 minutes), and centrifuged to get clear supernatant. (This procedure of deproteinization insures the elimination of danger for the spontaneous increase in ammonia reading which may arise while the mixture of blood with deproteinzing reagent is allowed to stand at room temperature). 3゜. Coloration. The deproteinzed supernatant of blood (0.5 ml) is mixed with  phenol-nitroprusside solution (2.0 ml) and antiformin solution (2.0 ml), mixed and incubated at 37℃ (for 3 minutes). (A stable blue coloration which is not disturbed by the co-existing non-NH_3 nitrogen substances is obtained in this way.)  4゜. The standard solutions of ammonium sulfate (1.0 ml aliquots 
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        departmental bulletin paper
    
    
        
            Publishers
        
            Yamaguchi University Graduate School of Medicine
    
    
        
            Date Issued
        
        1968-09
    
    
        
            File Version
        
        Version of Record
    
    
        
            Access Rights
        
        open access
    
    
            Relations
        
            
                
                
                [ISSN]0513-1812
            
            
                
                
                [NCID]AA00594272
            
    
        
            Schools
        
            医学部
    
                
