Abstract: | Objective :The catalpol in radix rehmanniae was determination by HPLC. Methods: Catalpol was separated on a ODSC18 column using water acetonitrile (99.4 0.6 )as mobile phase,and detection at210 nm. Results: There was a good linearity ranging from 2 to 10g of catalpol(Y=11 236.6+3 174 626X,r=0.999 3).The average recovery was 99.1%. Conclusion: The method is constant and have a good concentration.It is good method for determination of catalpol in radix rehmanniae enriched grain. |