Hunan Engineering Technology Research Center of Veterinary Drugs, Hunan Agricultural University, Changsha, Hunan 410128, China; College of Veterinary Medicine, Hunan Agricultural University, Changsha, Hunan 410128, China.
Hunan Provincial Institute of Veterinary Drugs and Feed Control, Changsha, Hunan 410006, China.
J Pharm Biomed Anal. 2019 Nov 30;176:112833. doi: 10.1016/j.jpba.2019.112833. Epub 2019 Aug 23.
The multicomponent pharmacokinetic study of herbal medicine is a great challenge due to the low plasma concentrations, large range of concentration scales, lack of authentic standards and uncertain interactions of the components. The aim of this work was to explore the in vivo pharmacokinetics of herbal medicine independently of authentic standards using an integrated analytical strategy. First, ion pairs of multiple components were tuned and selected, and then major parameters were optimized for derivative multiple reaction monitoring (DeMRM) by LC-MS/MS, which was combined with characterization of the chemical profiles of the herbal medicine by LC-QqTOF/MS. Second, different concentrations of herbal extracts were employed instead of authentic standards to construct calibration curves for the semiquantitative determination of multiple components in plasma. Taking Gelsemium elegans as an example, in addition to the fully validated and sufficient methodological results, a total of 27 alkaloid components, major bioactive constituents of Gelsemium elegans, were simultaneously monitored in pig plasma. The concentration-time profiles and pharmacokinetic properties of these 27 components were characterized. The absolute quantification of three components was compared with the results obtained using authentic standards, and the method showed very similar analytical characteristics, such as linearity, precision, accuracy, and the values of the pharmacokinetic parameters T, Vd, Cl and MRT. This analytical strategy was found to be capable of assessing herbal pharmacokinetics independently of specific authentic compounds for each component. This study was the first attempt to systematically reveal the in vivo pharmacokinetics of Gelsemium elegans. This strategy and methodology will find widespread use in the quantitative pharmacokinetic analysis of multiple components independently of standards for herbal medicine, among other applications.
草药的多成分药代动力学研究是一个巨大的挑战,这是由于其血浆浓度低、浓度范围大、缺乏真实标准以及成分相互作用不确定等原因所致。本工作的目的是探索一种独立于真实标准的草药体内药代动力学的分析策略。首先,我们对多种成分的离子对进行了调谐和选择,然后通过 LC-MS/MS 对衍生多重反应监测(DeMRM)的主要参数进行了优化,这与通过 LC-QqTOF/MS 对草药的化学成分进行特征描述相结合。其次,我们使用不同浓度的草药提取物代替真实标准来构建校准曲线,用于半定量测定血浆中的多种成分。以钩吻为例,除了完全验证和充分的方法学结果外,我们还同时监测了猪血浆中 27 种生物碱成分,这些生物碱成分是钩吻的主要生物活性成分。对这些 27 个成分的浓度-时间曲线和药代动力学性质进行了描述。与使用真实标准获得的结果相比,对三种成分的绝对定量进行了比较,该方法表现出非常相似的分析特征,如线性、精密度、准确度以及药代动力学参数 T、Vd、Cl 和 MRT 的值。这种分析策略被发现能够独立于每种成分的特定真实化合物来评估草药的药代动力学。本研究首次尝试系统地揭示钩吻的体内药代动力学。该策略和方法将广泛应用于独立于标准的草药多成分定量药代动力学分析,以及其他应用。