| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1222580 | Journal of Pharmaceutical and Biomedical Analysis | 2012 | 4 Pages |
A simple and selective method was developed for the simultaneous determination of tetrandrine and fangchinoline in herbal medicine by HPLC with electrochemical detection (ECD) on a bare glassy carbon electrode. The HPLC separation and ECD conditions have been optimized. The separation was carried out on a WondaSil® C18-WR column (4.6 mm × 250 mm, 5 μm), with the mobile phase of acetonitrile–ammonium acetate buffer (pH 6.5; 40 mM) (32:68, v/v) using an isocratic elution at the flow rate of 0.5 mL/min. The electrochemical detection potential was set at +0.9 V. The obtained LODs for tetrandrine and fangchinoline were 0.26 and 0.27 μmol/L, respectively. The method was successfully applied to the analysis of tetrandrine and fangchinoline contents in Stephania tetrandra S. Moore. It has been demonstrated that the LC-ECD method is an excellent technique for analysis of the herbal medicine. The mean recoveries were in the range of 95–105%, while the precision expressed as repetition of peak area was lower than 2.7%.
► Selective and sensitive method of liquid chromatography-electrochemical detection. ► Analysis of active components of tetrandrine and fangchinoline in Chinese herb. ► High sensitive with limit of detection 270 nM. ► Less interference from complex matrix in real sample. ► LC–MS identification and confirmation.
