Fructus Psoraleae, the dried fruits of Psoralea corylifolia L., is one of the most popular traditional Chinese medicine and is officially listed in the Chinese Pharmacopoeia. This crude drug has been used for the treatment of enuresis, pollakiuria, weak kidney, and pain and cold in the waist and knees. It always attracts research interest from various related fields. Last year, over ten articles have been published with focus on its quality analyses, [1][2][3] phytochemistry, [4][5][6][7][8] and bioactivities.9-16) Our previous phytochemical investigation on this medicinal herb revealed two new benzofuran glycosides, psoralenoside (1) and isopsoralenoside (2), using high performance liquid chromatography mass spectroscopy (HPLC-MS) technique. 17) They were found to have interesting structures which were related to the major constituents of Fructus Psoraleae, psoralen (3) and isopsoralen (4). From the chemistry point of view, psoralen and isopsoralen could be the products of the hydrolyzation of these two new benzofuran glycosides. However, all the previously reported quality analyses of this important herbal medicine were focused on coumarins (3) and (4). Therefore, we carried out a new quality research using both glycosides (1) and (2) and coumarins (3) and (4) as the quality markers, which led to the discovery of some attractive relationships between these chemical markers.
ExperimentalReagents and Materials Twenty-three batches of the raw material of Fructus Psoraleae were collected from different regions of China and they were authenticated as genuine P. corylifolia according to their morphological characteristics. The voucher specimens were deposited in the Chinese Medicine Laboratory of Hong Kong Jockey Club Institute of Chinese Medicine. The reference chemical standards of psoralen (batch No. 110739-200309) and isopsoralen (batch No. 110738-200410) were purchased from the National Institute for the Control of Pharmaceutical and Biological Products of China (Beijing, China). Psoralenoside and isopsoralenoside were isolated and purified as described in our previous report.17) The purities of the chemical references were determined to be beyond 98% by HPLC analysis. HPLC grade methanol and acetic acid were purchased from International Laboratory (Nevada, U.S.A.). HPLC grade water was prepared by Millipore Milli-Q SP water purification system.
Apparatus and ColumnThe Agilent 1100 series HPLC system equipped with a Zorbax ® XDB-C 8 analytical column (4.6ϫ150 mm, 5 mm, Agilent Technologies, U.S.A.), a C 18 guard column (4.6ϫ12.5 mm, 5 mm, Agilent Technologies, U.S.A.) and a photodiode array detector (DAD) was set up for the analysis. The analysis was performed at 20°C during the whole process. The mobile phase was a mixture of methanol and water (containing 0.1% acetic acid) at a flow rate of 1.0 ml/min. Linear gradient elution from 25 to 60% methanol (v/v) in 30 min was applied. The detection wavelength was set at 246 nm.Standard Solutions The stock solutions were prepared in methanol at the concentrations ...