| Abstract: | Semen Sojae Preparatum is one of the most widely used traditional Chinese medicines. A reliable and accurate high‐performance liquid chromatography with diode array detection method has been developed and validated for the quantitative determination of the ten bioactive compounds contained in Semen Sojae Preparatum. The samples were first extracted by pressurized liquid extraction using 80% ethanol at 100°C for 15 min and three static extraction cycles. Chromatographic separation was conducted on a C18 column using a mobile phase consisting of water and acetonitrile under gradient elution, and the detection wavelength was set at 210 nm. The samples were further analyzed on a high‐performance liquid chromatography with time‐of‐flight mass spectrometry system to confirm the determination results. All the ten analytes were well separated, and the calibration curves showed good linearity. The intra‐ and interday precisions were evaluated in terms of relative standard deviation values within the ranges of 0.20–1.43% and 0.40–4.78%, respectively. The recoveries for the ten analytes were all in the ranges of 96.2–104.3%, with relative standard deviation values < 3.85%. The established high‐performance liquid chromatography method could serve as a reliable and accurate method for the quality evaluation of Semen Sojae Preparatum from different origins. |
