Determination of Three Xanthone Glycosides in Gentianella Acuta by HPLC
	    		
		   		
		   			 
		   		
	    	
    	 
    	10.11842/wst.2014.05.020
   		
        
        	
        		- VernacularTitle:HPLC法测定尖叶假龙胆中3个[口山]酮苷的含量
- Author:
	        		
		        		
		        		
			        		Qian WEI
			        		
			        		;
		        		
		        		
		        		
			        		Tonghua LIU
			        		
			        		;
		        		
		        		
		        		
			        		Xiaojuan SHI
			        		
			        		;
		        		
		        		
		        		
			        		Pengshou LI
			        		
			        		;
		        		
		        		
		        		
			        		Ying WEI
			        		
			        		;
		        		
		        		
		        		
			        		Tunhai XU
			        		
			        		
		        		
		        		
		        		
 
			        		
			        		
		        		 
- Publication Type:Journal Article
- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Gentianella acuta;
			        		
			        		
			        		
				        		Xanthone glycosides;
			        		
			        		
			        		
				        		content determination;
			        		
			        		
			        		
				        		HPLC
			        		
			        		
	        			
        			
        		
- From:
	            		
	            			World Science and Technology-Modernization of Traditional Chinese Medicine
	            		
	            		 2014;(5):1060-1064
	            	
            	
- CountryChina
- Language:Chinese
- 
		        	Abstract:
			       	
			       		
				        
				        	To develop a method for determining 3 Xanthone glycosides (1, 5-dihydroxy- 3-methoxyxanthone 8-O-β-D-glucopyranoside(F1), 1-hydroxy-3, 4-dimethoxyxanthon 7-O-β-D-glucopyranoside (F2), 1, 8-dihydroxy-3, 4-dimethoxyxanthone 5-O-β- D-glucopyranoside (F3) of Gentianella acuta by HPLC. The Thermo syncronis C18 (4.6 mmí250 mm, 5 μm) was used for simultaneous determination of 3 Xanthone glycosides in G. acuta. Isocratic elution with water and acetonitrile was 75.5:24.5. The flow rate was 1.0 mL·min-1 and the detection wavelength was set at 254 nm. The column temperature was 35℃. The linear concentration ranges of F1,F2,F3 were 14.06 ~ 281.28 μg·mL-1 (R2=0.999 7),0.56~11.16 μg·mL-1 (R2=0.999 8),0.46~9.20 μg·mL-1 (R2=0.999 9), respectively; The average recov-eries (n = 9) were 99.70% (RSD=1.06%),99.78% (RSD=1.21%),100.28% (RSD=1.15%), respectively. The method is simple, accurate and sensitive, and can be used for the quality control of G. acuta as a reference.