Abstract
Background: With significant clinical effects, traditional Chinese medicine (TCM) has been attracting
increasing interest of the world’s scientific community. However, TCM contains immense amounts of chemical
components. It is a great challenge to objectively evaluate the correlation between the in vivo process and the therapeutic
effect of TCM. The purpose of this systematic review was to summarize the recent investigation (from 2017 to
2019) on preclinical pharmacokinetics (PK) of TCM via liquid chromatography coupled with mass spectrometry
(LC-MS/MS).
Methods: We reviewed the published articles regarding the PK of TCM by LC-MS/MS. In addition, we summarized
information on PK parameter of bioactive components, single herb and traditional Chinese medicine prescriptions.
Results: The vast majority of literature on preclinical PK of TCM uses single oral administration, the biological
matrix is mostly rat plasma, and the main PK parameters include AUC, Cmax, Tmax and T1/2, etc.
Conclusion: Although LC-MS/MS can be used for high-throughput analysis, the characterization of in vivo processes
of TCM still has a long way. With the advantages of high sensitivity, high specificity and simple operation, the
increasingly mature LC-MS/MS technology will play an important role in the PK study of TCM.
Keywords:
Traditional Chinese medicine, LC-MS/MS, pharmacokinetics, quantitative analysis, bioactive components, pharmacodynamic
material basis.
Graphical Abstract
[5]
Wang, X.J. Studies on serum pharmacochemistry of traditional Chinese medicine, world science and technology: modernization of traditional. Chin. Med., 2002, 4(2), 1-4.
[13]
Zhou, Mengying H.X.; Wang, Y. Analysis of pharmacokinetics of sanguisorbin II in rats by UPLC-MS/MS. Chinese J. of Exp. Prescriptions, 2018, 24(21), 86-90.
[15]
Xiao-liang, Z.; Tao, L.; Yang, L.; Mei-yu, Z.; Yue, C.; Ying, Z.; Dan-dan, S.; Zhi-guo, W.; Dan-qiou, W. Pharmacokinetic analysis of sinomenine based on automatic blood collection system and hplc-qqq-ms. Chinese J. of Exp. Prescriptions, 2015, 14, 66-70.
[17]
Liu, S-G.; Dai, X-J.; Zhong, D-F.; Zhang, C-F. Identification of metabolites and pharmacokinetics of mogrol in rat plasma. Acta Pharm. Sin., 2017, 52(9), 1452-1457.
[18]
Bai, Junqi. H.J.; Wen, X.; Jing, Z.; Lu, G.; Huang, Z.; Qiu, X. Study on pharmacokinetics of dendrobine in rats by LC-MS/MS, World traditional. Chin. Med., 2019, 14, 2272-2275.
[20]
Xie Yao, Z.N. Pharmacokinetic study on the main component of hyssop in Pearl lotus. J. SYMC., 2018, 4, 332-335.
[23]
Zhang , Zhe T.Y.; Ziyan, L.V. Pharmacokinetic behavior and metabolites of ginsenoside Rb2 in rats. Anal. Chem., 2017, 02, 50-57.
[39]
Yu, Weibang, J.Z.; Jian, Y. Pharmacokinetics of curcumin monomer and curcumin extract in rats, Pharmacology and clinic of traditional. Chin. Med., 2018, 34, 32-35.
[40]
Li, Zhining W.Y.; Jie, Z. Determination of curcumin in rat plasma by ultra high performance liquid chromatography mass spectrometry. Henan Science, 2017, 008, 1252-1257.
[84]
Shen, J.; Wei, J.; Li, L.; Ouyang, H.; Chang, Y.; Chen, X.; He, J. Development of a HPLC-MS/MS method to determine 11 bioactive compounds in Tongmai Yangxin pill and application to a pharmacokinetic study in rats. Evid. Based Complement. Alternat. Med., 2018, 2018(3), 1-11.