Fujii Y, Ikeda Y, Yamazaki M
School of Pharmacy, Hokuriku University, Japan.
J Chromatogr. 1989 Oct 6;479(2):319-25. doi: 10.1016/s0021-9673(01)83346-x.
An analytical method for the determination of secondary cardiac glycosides in Digitalis purpurea leaves by high-performance liquid chromatography (HPLC) is described. The procedure consisted of extraction of dry leaf powder with ethanol-chloroform (2:1) and clean-up by Sep-Pak cartridges prior to HPLC analysis. HPLC was performed on an octylsilyl bonded silica column, using acetonitrile-methanol-water (4:4:5) for trisdigitoxosides and acetonitrile-methanol-water (8:30:43) for strospeside; the effluent was monitored by ultraviolet detection (at 220 nm). Quantitation of these cardiac glycosides was carried out by the internal standard method. The amounts of digitoxin, gitoxin, gitaloxin and strospeside per 100 mg of dry leaf powder were estimated to be 22.6, 14.0, 54.7 and 1.9 micrograms, respectively. The method is sufficiently sensitive and reproducible to assay secondary glycosides in Digitalis purpurea leaves.
描述了一种用高效液相色谱法(HPLC)测定紫花洋地黄叶中次生强心苷的分析方法。该方法包括用乙醇 - 氯仿(2:1)提取干叶粉,并在HPLC分析前用Sep - Pak柱进行净化。HPLC在辛基甲硅烷基键合硅胶柱上进行,对于洋地黄毒三糖苷,使用乙腈 - 甲醇 - 水(4:4:5),对于加拿大麻苷,使用乙腈 - 甲醇 - 水(8:30:43);流出物通过紫外检测(在220nm处)进行监测。这些强心苷的定量采用内标法进行。每100mg干叶粉中洋地黄毒苷、吉托辛、吉他洛辛和加拿大麻苷的含量分别估计为22.6、14.0、54.7和1.9微克。该方法对于测定紫花洋地黄叶中的次生苷具有足够的灵敏度和重现性。