Lin Shuhai, Wang Dongmei, Yang Depo, Yao Junhua, Tong Yao, Chen Jianping
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Anal Chim Acta. 2007 Sep 5;599(1):98-106. doi: 10.1016/j.aca.2007.07.070. Epub 2007 Aug 3.
The liquid chromatography-electrospray ionization-tandem multi-stage mass spectrometry (LC-ESI-MS(n)) method was developed for the analyses and characterization of steroidal saponins in plant extract from the rhizome of Dioscorea nipponica Makino. The HPLC experiments were performed by means of a reversed-phase C18 column and a binary mobile phase system consisting of water and acetonitrile under gradient elution conditions. Pseudoprotodioscin, methyl protodioscin and dioscin were identified by comparing the retention times, UV spectra and the fragmentation properties of [M-H]- ions with the authentic standards. Four groups of steroidal saponin isomers possessed the [M-H]- ions at m/z 1063, 1045, 901 and 1047, respectively, were observed during the LC-ESI(-)-MS analysis, and three groups of them except the pair of isomers with the [M-H]- ions at m/z 1047 could be differentiated by LC-ESI(-)-MS3. Furthermore, the ESI-MS(n) fragmentation behaviors of the [M+Li]+ ions of pseudoprotodioscin and methyl protodioscin have been investigated, and the observed information helped the structural elucidation of the more abundant isomer with the [M-H]- ion at m/z 1047. As the result, a special sugar sequence of the saccharide chains was observed that not glucose but rhamnose might be connected with the hydroxyl group at C-3 position of the steroidal aglycone.
建立了液相色谱-电喷雾电离-串联多级质谱法(LC-ESI-MS(n)),用于分析和表征来自穿山龙根茎植物提取物中的甾体皂苷。高效液相色谱实验采用反相C18柱和由水和乙腈组成的二元流动相系统,在梯度洗脱条件下进行。通过比较伪原薯蓣皂苷、甲基原薯蓣皂苷和薯蓣皂苷的保留时间、紫外光谱以及[M-H]-离子的碎裂特性与标准品来进行鉴定。在LC-ESI(-)-MS分析过程中,观察到四组甾体皂苷异构体分别具有m/z 1063、1045、901和1047的[M-H]-离子,除了具有m/z 1047的[M-H]-离子的那对异构体之外,其中三组可以通过LC-ESI(-)-MS3进行区分。此外,还研究了伪原薯蓣皂苷和甲基原薯蓣皂苷的[M+Li]+离子的ESI-MS(n)碎裂行为,所观察到的信息有助于阐明具有m/z 1047的[M-H]-离子的含量较高的异构体的结构。结果发现,糖链存在一种特殊的糖序列,即与甾体苷元C-3位羟基相连的不是葡萄糖而是鼠李糖。