Li Zhen, Li Yang, Li Jin, Liu Rui, Hao Jia, He Jun, Chang Yan-Xu
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Tianjin Key Laboratory of Phytochemistry and Pharmaceutical Analysis, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Int J Anal Chem. 2019 Feb 13;2019:1639619. doi: 10.1155/2019/1639619. eCollection 2019.
A sensitive and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to simultaneously determine the toxic and other active components including isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of extract to rats. Plasma samples were prepared by protein precipitation with methanol. All compounds were separated on a C column with gradient elution using acetonitrile and formic acid aqueous solution (0.1%, ) as the mobile phase at a flow rate of 0.3 mL/min. The detection of all compounds was accomplished by multiple-reaction monitoring (MRM) in the positive electrospray ionization mode. The LC-MS/MS method exhibited good linearity for five analytes. The lower limit of quantification (LLOQ) was 0.48 ng/mL for scopoletin, periplogenin, and periplocymarin; 2.4 ng/mL for isovanillin and periplocin. The extraction recoveries of all compounds were more than 90% and the RSDs were below 10%. It was found that the absorption of scopoletin and periplocin was rapid after oral administration of extract. Furthermore, periplocymarin possessed abundant plasma exposure. The results demonstrated that the validated method was efficiently applied for the pharmacokinetic studies of isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of extract.
建立并验证了一种灵敏且简便的液相色谱-串联质谱(LC-MS/MS)方法,用于在给大鼠口服提取物后同时测定包括异香草醛、东莨菪内酯、杠柳毒苷、杠柳苷元及杠柳氰苷在内的有毒及其他活性成分。血浆样品通过甲醇蛋白沉淀法制备。所有化合物在C柱上分离,以乙腈和甲酸水溶液(0.1%,)作为流动相进行梯度洗脱,流速为0.3 mL/min。所有化合物的检测通过正电喷雾电离模式下的多反应监测(MRM)完成。该LC-MS/MS方法对五种分析物表现出良好的线性。东莨菪内酯、杠柳苷元及杠柳氰苷的定量下限(LLOQ)为0.48 ng/mL;异香草醛和杠柳毒苷为2.4 ng/mL。所有化合物的提取回收率均超过90%,相对标准偏差低于10%。结果发现,口服提取物后,东莨菪内酯和杠柳毒苷的吸收迅速。此外,杠柳氰苷具有较高的血浆暴露量。结果表明,该验证方法可有效地应用于口服提取物后异香草醛、东莨菪内酯、杠柳毒苷、杠柳苷元及杠柳氰苷的药代动力学研究。