Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 312 Anshanxi Road, Tianjin 300193, China.
Tianjin Key Laboratory of TCM Chemistry and Analysis, Tianjin University of Traditional Chinese Medicine, 312 Anshanxi Road, Tianjin 300193, China.
Molecules. 2018 Nov 30;23(12):3143. doi: 10.3390/molecules23123143.
The analytical platform UHPLC/Q-Orbitrap-MS offers a solution to quality investigation of TCM with high definiteness. Using Erzhi Pill (EZP) as a case, we developed UHPLC/Q-Orbitrap-MS based approaches to achieve systematic multicomponent identification and rapid authentication. Comprehensive multicomponent characterization of EZP was performed by negative/positive switching data-dependent high-energy collision-induced dissociation-MS² (HCD-MS²) after 25 min chromatographic separation. By reference compounds comparison, elemental composition analysis, fragmentation pathways interpretation, and retrieval of an in-house library, 366 compounds were separated and detected from EZP, and 96 thereof were structurally characterized. The fingerprints of two component drugs (Ligustri Lucidi Fructus, LLF; Ecliptae Herba, EH) for EZP were analyzed under the same LC-MS condition by full scan in negative mode. In combination with currently available pharmacological reports, eight compounds were deduced as the 'identity markers' of EZP. Selective ion monitoring (SIM) of eight marker compounds was conducted to authenticate six batches of EZP samples. Both LLF and EH could be detected from all EZP samples by analyzing the SIM spectra, which could indicate their authenticity. Conclusively, UHPLC/Q-Orbitrap-MS by rapid polarity switching could greatly expand the potency of untargeted profiling with high efficiency, and SIM of multiple chemical markers rendered a practical approach enabling the authentication of TCM formulae.
UHPLC/Q-Orbitrap-MS 分析平台为中药质量研究提供了高清晰度的解决方案。以二至丸(EZP)为例,我们开发了基于 UHPLC/Q-Orbitrap-MS 的方法,以实现系统的多组分鉴定和快速鉴定。通过 25 分钟的色谱分离后,采用正负切换数据相关高能碰撞诱导解离-MS²(HCD-MS²)对 EZP 进行全面的多组分特征化。通过参考化合物比较、元素组成分析、碎裂途径解释和内部库检索,从 EZP 中分离和检测到 366 种化合物,其中 96 种化合物的结构得到了表征。在相同的 LC-MS 条件下,通过负模式全扫描分析了二至丸中两种成分药物(女贞子、旱莲草)的指纹图谱。结合目前可用的药理学报告,推断出 8 种化合物为 EZP 的“特征标志物”。对 8 种标记化合物进行选择离子监测(SIM),以鉴定 6 批 EZP 样品。通过分析 SIM 谱图,可以从所有 EZP 样品中检测到女贞子和旱莲草,这表明它们的真实性。总之,通过快速极性切换的 UHPLC/Q-Orbitrap-MS 可以极大地提高非靶向分析的效率,并通过多个化学标志物的 SIM 实现了一种实用的方法,能够对中药配方进行鉴定。