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Xenobiotica
the fate of foreign compounds in biological systems
Volume 46, 2016 - Issue 12
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Animal Pharmacokinetics and Metabolism

Pharmacokinetic comparisons of Paeoniflorin and Paeoniflorin-6'O-benzene sulfonate in rats via different routes of administration

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Pages 1142-1150 | Received 29 Oct 2015, Accepted 29 Jan 2016, Published online: 21 Mar 2016
 

Abstract

1. The pharmacokinetics study of Paeoniflorin (Pae) and its acylated derivative (CP-25) was performed.

2. The structure of CP-25 was identified by mass spectrometry (MS) and nuclear magnetic resonance spectroscopy (NMR). The rats were injected with CP-25(6, 12, 24 mg/kg) and orally treated with CP-25 (32, 64, 128 mg/kg), respectively. An high-performance liquid chromatography (HPLC) assay was developed to determine the plasma concentrations of Pae and CP-25.

3. The results of MS and NMR showed that the acylated product was Pae-6'O-benzene sulfonate (CP-25). The plasma levels in oral CP-25 groups were detectable, whereas those of Pae in the oral groups (25 and 50 mg/kg) were undetectable. More specifically, the Cmax values of oral CP-25 were 0.12, 0.19 and 0.44 μg/ml, and the corresponding t1/2β of CP-25 were 1.44, 2.12 and 2.11 h, respectively. In addition, the t1/2β values of intravenous CP-25 were 161.99, 152.81 and 153.76 min, respectively.

4. Compared with the venous pharmacokinetics parameters of Pae, those of the t1/2β, MRT, Vd and CL/F in the CP-25 groups increased noticeably. As expected, compared with oral parameters of Pae, those of t1/2a, t1/2β, AUC, MRT and Vd in the CP-25 group increased obviously. Finally, the absolute bioavailability of Pae and CP-25 were 3.6 and 10.6%, respectively.

5. Our results indicate that CP-25 is characterized by improved absorption, well distribution, lower clearance, long mean residence time, and moderate bioavailability in rats.

Acknowledgements

The authors would like thank Prof. Jin-qi Liu (Anhui University of Chinese Medicine), Prof. Yu-hua Sheng (Anhui University), Dr. Qing-bo Yu (Anhui University) and Dr. An Zhou (Anhui University of Chinese Medicine) for their excellent technical assistance.

Declaration of interest

The authors declare that they have no conflict of interest. This work was financially supported by the National Natural Science Foundation of China (No.81330081, No.81302845, and No.81473223), the Training Program of Academic and Technical Leaders in the Universities of Anhui Province (No. 34), the Anhui Province Nature Science Foundation in the University (No. KJ2013A158) and the Grants for Scientific Research of BSKY (No.XJ201211) from Anhui Medical University.

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