Dual-label Time-resolved Fluoroimmunoassay for Pepsinogen Ⅰ and Pepsinogen Ⅱ and Its Preliminary Application
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:胃蛋白酶原双标记时间分辨荧光免疫分析及其初步临床应用
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jue ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Biao HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Lan ZHU
			        		
			        		;
		        		
		        		
		        		
			        		Yi ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Haiyan LIU
			        		
			        		;
		        		
		        		
		        		
			        		Zhihong MA
			        		
			        		;
		        		
		        		
		        		
			        		Lining GUO
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		pepsinogenⅠ, pepsinogenⅡ, dual-label, time-resolved fluoroimmunoassay
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Progress in Biochemistry and Biophysics
	            		
	            		 2006;0(04):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	A dual-label time-resolved fluoroimmunoassay was established for simultaneously detecting pepsinogen Ⅰ (PGⅠ) and pepsinogen Ⅱ (PG Ⅱ) in human serum. Two capture monoclonal antibodies, 8003# of PGⅠ and 8101# of PGⅡ, were co-coated in 96 microtitration wells. The counterpart tracer monoclonal antibodies, 8016# of PGⅠ and 8102# of PGⅡ, were labeled with Eu3+ and sm3+-chelates, respectively. The samples were assayed by one-step sandwich protocol with the time-resolved fluorometry. The measurement ranges of PGⅠ were 0.2~300.0 ?g/L with the within-run and between-run precision was 5.2% and 8.1%, and that of PGⅡ were 0.05~55.0 ?g/L with the within-run and between-run precision was 7.1% and 11.7%, respectively. The average recovery rates of PGⅠ and PGⅡ were 96.9% and 103.7%, respectively. The results obtained by the dual-label assay agreed well with those by enzyme-linked immunosorbent assays of PGⅠ and PGⅡ, whose correlation ratio were 0.9426 of PGⅠ and 0.9396 of PGⅡ, respectively. The means of 300 healthy volunteers were (157.3 ? 51.0) ?g/L for serum PGⅠ,(10.6 ? 5.9) ?g/L for serum PGⅡ, and (14.8 ? 4.3) for the PGⅠ/PGⅡ ratio. The normal ranges of serum PGⅠ levels for healthy volunteers were 55.3~259.3 ?g/L, those of serum PGⅡ levels were less than 23 ?g/L, the PGⅠ/PGⅡ ratio was more than 6. The proposed dual-label TRFIA for simultaneous detection of PGⅠ and PGⅡ is a simple, sensitive, and rapid method. It could provide serology high-screening of the samples for gastric diseases and would allow investigations into the possible diagnostic value of analysis in various clinical condition.