Planta Med 2016; 82(03): 230-237
DOI: 10.1055/s-0035-1558207
Pharmacokinetic Investigations
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Comparison of Pharmacokinetics and Biodistribution of 10-Deacetylbaccatin III after Oral Administration as Pure Compound or in Taxus chinensis Extract: A Pilot Study

Xueli Zhang*
1   Department of Pharmacy, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China
,
Jiajia Lv*
2   School of Pharmaceutical Sciences, Zunyi Medical University, Zunyi, China
3   School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China
,
Liling Wang
3   School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China
,
Hua Shao
1   Department of Pharmacy, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China
› Author Affiliations
Further Information

Publication History

received 01 June 2015
revised 21 September 2015

accepted 26 September 2015

Publication Date:
02 February 2016 (online)

Abstract

Taxanes are a class of bioactive compounds isolated from the Taxus species. 10-Deacetylbaccatin III is one of the popular taxane compounds with antitumor activity, but the pharmacokinetic profile of this compound remains elusive. Previously, we prepared the taxane fractions from the twigs and leaves of Taxus chinensis var. mairei containing 20.4 % 10-deacetylbaccatin III. This study aimed to investigate the pharmacokinetics of 10-deacetylbaccatin III and biodistribution, and explore the potential changes when it was administered in the form of taxane extracts. A simple, sensitive, and reliable liquid chromatography-tandem mass spectrometry method was developed and validated for the quantitative determination of 10-deacetylbaccatin III in biosamples. The results showed that 10-deacetylbaccatin III, after oral dosing, displayed a quick absorption into the blood and distribution into major organs. Oral administration of 10-deacetylbaccatin III in the form of taxane mixtures led to a 16-fold increase in the systemic exposure of pure 10-deacetylbaccatin III, with the AUC0-U in the plasma increasing from 25.75 ± 11.34 to 231.36 ± 70.12 µg h/L (p < 0.0001). Moreover, the concentrations of 10-deacetylbaccatin III in major tissues were significantly enhanced when given in taxane extracts. These findings revealed pharmacokinetic interactions in the taxane components from T. chinensis var. mairei, which contributed to an enhanced systemic exposure of pharmacologically active taxanes.

* These two authors contributed equally to this work.


 
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