Citation

Wang LL, Zhao DS, Shi W, Li ZQ, Wu ZT, Li P, Li HJ. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2017; 1064: 40-48.

Affiliation

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China. Electronic address: cpuli@163.com.

Copyright

(Copyright © 2017, Elsevier Publishing)

DOI

10.1016/j.jchromb.2017.08.040

PMID

28910661

Abstract

It is vital to monitor the holistic toxicokinetics of toxic Chinese herbal medicines (CHMs) for safety. Although an integrated strategy based on the area under the curve (AUC) has been proposed to characterize the pharmacokinetic/toxicokinetic properties of CHMs, improvement is still needed. This study attempted to use 50% inhibitory concentration (IC50) as weighting coefficient to investigate holistic toxicokinetics of the major diosbulbins i.e. diosbulbin A (DA), diosbulbin B (DB), and diosbulbin C (DC) after oral administration of Dioscorea bulbifera rhizome (DBR) extract. Firstly, the cytotoxicities of the three diosbulbins on human hepatic L02 cells were evaluated and the IC50 values were calculated. Then, integrated toxicokinetics of multiple diosbulbins based on AUC and IC50 were determined. Finally, correlations between integrated plasma concentrations and hepatic injury biomarkers including alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and total bile acid (TBA) were analyzed. As a result, integrated plasma concentrations were correlated well with TBA and the correlation between TBA and IC50-weighting integrated plasma concentrations was better than that of AUC-weighting integrated plasma concentrations. In conclusion, the newly developed IC50-weighting method is expected to generate more reasonable integrated toxicokinetic parameters, which will help to guide the safe usage of DBR in clinical settings.

Copyright © 2017 Elsevier B.V. All rights reserved.

Language: en

Keywords

Dioscorea bulbifera rhizome; Hepatotoxicity; IC(50); Integrated toxicokinetics; LC-QqQ-MS