Characterization and identification of steroidal saponins from the seeds of Trigonella foenum-graecum by ultra high-performance liquid chromatography and hybrid time-of-flight mass spectrometry

• Published in: Journal of pharmaceutical and biomedical analysis 2013-02, Vol.74, p.257-267
• Main Authors: Kang, Li-ping, Zhao, Yang, Pang, Xu, Yu, He-shui, Xiong, Cheng-qi, Zhang, Jie, Gao, Yue, Yu, Kate, Liu, Chao, Ma, Bai-ping
• Format: Article
• Language: English
• Subjects: Chromatography, High Pressure Liquid - methods; ions; isomers; mass spectrometry; Phytosterols - analysis; Phytosterols - chemistry; Plant Extracts - analysis; Plant Extracts - chemistry; Rapid structural identification; reference standards; Saponins - analysis; Saponins - chemistry; seeds; Seeds - chemistry; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods; steroid saponins; Steroidal saponins; Tandem Mass Spectrometry - methods; Traditional Chinese medicine; Trigonella - chemistry; Trigonella foenum-graecum; UHPLC/Qtof MSE; ultra-performance liquid chromatography
• ISSN: 0731-7085; 1873-264X
• DOI: 10.1016/j.jpba.2012.11.005

95 saponins were identified or tentatively identified, including 30 new saponins. [Display omitted] ► A method was used to separate and identify steroidal saponins in fenugreek seeds. ► Fragmentation patterns for five groups of known saponins were investigated. ► 95 saponins were identified or tentatively identified. ► Thirty of them may be new compounds. ► This method is efficient to identify constituents in complex samples. Ultra high-performance liquid chromatography (UHPLC) coupled with hybrid quadrupole time-of-flight mass spectrometry (Qtof MSE) was used to rapidly separate and identify steroidal saponins from the crude extract of the seeds of Trigonella foenum-graecum (TFG). By using the UHPLC/Qtof MSE data acquisition strategy, both intact precursor and fragment ion information were obtained from a single injection. Fragmentation rules for five major groups of saponins from TFG are summarized, and possible fragmentation pathways are proposed. Accurate mass measurements of molecular ions and fragment ions as well as retention times permitted the identification or tentative identification of a total of ninety-five saponins based on comparison with reference standards. This included twenty-two pairs of isomers. Thirty of these saponins were identified for the first time.