线性范围                        
                
                                
                        
                            核化学                        
                
                                
                        
                            试剂                        
                
                                
                        
                            过氧化氢                        
                
                                
                        
                            相对标准差                        
                
                                
                        
                            抗坏血酸                        
                
                                
                        
                            无机化学                        
                
                        
                    
            作者
            
                D. Easwaramoorthy,Yueh-Chuan Yu,Hsuan‐Jung Huang            
         
                    
        
    
            
            标识
            
                                    DOI:10.1016/s0003-2670(01)00968-0
                                    
                                
                                 
         
        
                
            摘要
            
            The flow injection analysis of paracetamol was developed based on its inhibitory effect on a luminol-permanganate chemiluminescence system. With a system containing solutions of 2.5 mM luminol, 5.0 μM KMnO4 and pH 12.0 phosphate buffer (K2HPO4/NaOH), a detection limit of 1.0×10−8 M (1.5 ppb) and a linear dynamic range of 2.5×10−8 to 2.5×10−7 M can be obtained. A repetitive injection of 1.0×10−7 M paracetamol solutions gave satisfactory reproducibility with a relative standard deviation of 2.3% (n=12). Possible interferences from major excipients in pharmaceuticals and other related compounds were also studied. Contents of paracetamol in two locally available pharmaceuticals were analyzed. From the recovery of 98.2–104.4% obtained, the feasibility of the developed method for real sample analysis was confirmed.
         
            
 
                 
                
                    
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