Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 151-742, Korea.
Phytochem Anal. 2013 Feb;24(2):148-54. doi: 10.1002/pca.2394. Epub 2012 Aug 29.
The roots of Adenophorae species have been reported to exhibit anti-obese, anti-oxidant, anti-cancer, and anti-bacterial activities. However, there has been no single report regarding the preparative isolation and biological activities of the chemical components from Adenophora triphylla.
To develop an efficient method for the determination of the active fraction from the methanol extract from the roots of Adenophora triphylla and for the preparative isolation and purification of target compounds having cytotoxicity on carcinoma cells from the active fraction by high-speed counter-current chromatography (HSCCC).
The Plant (5 kg, dry weight) was extracted with methanol. Three hundred grams of the dried methanol extract (885 g) were fractionated by open-column chromatography with a stepwise gradient of water-methanol. Preparative isolation of bioactive components was performed by HSCCC with a two-phase solvent system composed of ethyl acetate-n-butanol-0.2% trifluoroacetic acid in water (5:5:10, v/v). The cytotoxicity of column fractions and isolated compounds was evaluated by 2-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide assay.
The 70% MeOH column fraction showed inhibitory effects against three human carcinoma cells A549, AGS and HepG2. Two saponins were separated from 400 mg of the active fraction by HSCCC. After further purification with solid phase extraction column, 25 mg of peak fraction 1 and 20 mg of peak fraction 2 were obtained. Their structures were identified by ¹H-NMR, ¹³C-NMR, Fourier transform infrared, fast atom bombardment-MS and electrospray ionisation-MS/MS. They exhibited strong cytotoxic effects against three cancer cells.
Two cytotoxic saponins were isolated for the first time from the roots of Adenophora triphylla by HSCCC.
据报道,腺梗豨莶的根具有抗肥胖、抗氧化、抗癌和抗菌活性。然而,目前还没有关于从腺梗豨莶根中分离和提取具有细胞毒性的化学成分的单一报道。
开发一种从腺梗豨莶甲醇提取物中分离活性部位的有效方法,并通过高速逆流色谱(HSCCC)从活性部位中分离和纯化具有细胞毒性的目标化合物。
将植物(5 公斤,干重)用甲醇提取。将 300 克干燥的甲醇提取物(885 克)用梯度洗脱的正相柱色谱法,以水-甲醇为洗脱剂进行分离。采用两相溶剂体系(乙酸乙酯-正丁醇-0.2%三氟乙酸水溶液,5:5:10,v/v)进行 HSCCC 制备分离生物活性成分。通过 2-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法评估柱馏分和分离化合物的细胞毒性。
70%甲醇柱馏分对三种人癌细胞 A549、AGS 和 HepG2 均有抑制作用。从 400 毫克活性部位通过 HSCCC 分离得到两种皂苷。经固相萃取柱进一步纯化,得到峰 1 区 25 毫克和峰 2 区 20 毫克。通过 1H-NMR、13C-NMR、傅里叶变换红外光谱、快原子轰击质谱和电喷雾离子化质谱/质谱对其结构进行了鉴定。它们对三种癌细胞均表现出较强的细胞毒性。
首次通过 HSCCC 从腺梗豨莶根中分离得到两种具有细胞毒性的皂苷。