School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, PR China; Engineering Research Centre of Shanghai Colleges for TCM New Drug Discovery, Shanghai, 201203, PR China.
Solution Center, Waters Technologies Ltd. (Shanghai), Shanghai, 201203, PR China.
J Pharm Biomed Anal. 2019 Jan 30;163:24-33. doi: 10.1016/j.jpba.2018.09.036. Epub 2018 Sep 21.
Here, time-decoupled comprehensive two-dimensional ultra-high liquid chromatography (UHPLC) coupled with an ion mobility (IM)-high resolution mass spectrometer (HRMS) was established and used to analyze ginsenosides from the main roots of white ginseng (WG) and red ginseng (RG), which enabled the separation of complex samples in four dimensions (2D-LC, ion mobility, and mass spectrometry). The incompatibility of mobile phases, dilution effect, and long analysis time, which are the main shortcomings of traditional comprehensive 2D-LC methods, were largely avoided in this newly established 2D-UHPLC method. The orthogonality of this system was 55%, and the peak capacity was 4392. Under the optimized 2D-UHPLC-IM-MS method, 201 ginsenosides were detected from white and red ginseng samples. Among them, 10 pairs of co-eluting isobaric ginseng saponins that were not resolved by 2D-UHPLC-HRMS were further resolved using 2D-UHPLC-IM-MS. In addition, 24 ginsenoside references were analyzed by UHPLC-IM-MS to obtain their collision cross section (CCS) values and ion mobility characteristics. Finally, the established new method combined with multivariate statistical analysis was successfully applied to differentiate WG and RG, and 9 ginsenosides were found to be the potential biomarkers by S-Plot and the values of max fold change, which could be used for classifying WG and RG samples. Overall, the obtained results demonstrate the applicability and potential of the established time-decoupled online comprehensive 2D-UHPLC-IM-MS system, and it will be extended to the analysis of other targeted or untargeted compounds, especially co-eluting isomers in more herbal extracts.
这里,建立了时间分离的综合二维超高液相色谱(UHPLC)与离子淌度(IM)高分辨质谱(HRMS)联用,并用于分析白参(WG)和红参(RG)主根中的人参皂苷,实现了复杂样品在四个维度(2D-LC、离子淌度和质谱)上的分离。该新建立的 2D-UHPLC 方法在很大程度上避免了传统综合 2D-LC 方法中流动相不兼容、稀释效应和分析时间长等主要缺点。该系统的正交性为 55%,峰容量为 4392。在优化的 2D-UHPLC-IM-MS 方法下,从白参和红参样品中检测到 201 个人参皂苷。其中,10 对未通过 2D-UHPLC-HRMS 分离的同质量峰共洗脱人参皂苷,通过 2D-UHPLC-IM-MS 进一步分离。此外,通过 UHPLC-IM-MS 分析 24 个人参皂苷对照品,获得了它们的碰撞截面(CCS)值和离子淌度特征。最后,将建立的新方法与多元统计分析相结合,成功地用于区分 WG 和 RG,并通过 S-Plot 发现 9 个人参皂苷是区分 WG 和 RG 样品的潜在生物标志物,其最大倍数变化值可用于分类 WG 和 RG 样品。总的来说,所得到的结果证明了所建立的时间分离在线综合 2D-UHPLC-IM-MS 系统的适用性和潜力,该系统将扩展到其他靶向或非靶向化合物的分析,特别是在更多草药提取物中同质量峰共洗脱的异构体。