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Xenobiotica
the fate of foreign compounds in biological systems
Volume 49, 2019 - Issue 11
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Animal Pharmacokinetics and Metabolism

Pharmacokinetic interaction between shuanghuanglian and azithromycin injection: a nonlinear mixed-effects model analysis in rats

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Pages 1344-1351 | Received 10 Oct 2018, Accepted 16 Nov 2018, Published online: 18 Jan 2019
 

Abstract

1. This study aimed to evaluate the pharmacokinetic interaction of shuanghuanglian (SHL) and azithromycin in rats, and to provide experimental support for rational drug use in clinics.

2. High-performance liquid chromatography with ultraviolet detection (HPLC-UV) and high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) approaches were respectively developed to detect the forsythiaside (active component of SHL) and azithromycin concentrations. Both non-compartmental and compartmental analyzes were employed to calculate pharmacokinetic parameters. A nonlinear mixed-effects modeling method was applied to fit the drug concentration-time data. The influence of drug coadministration on pharmacokinetic parameters was tested using forward inclusion and backward elimination procedures.

3. After drug co-administration, areas under the drug concentration–time curve (AUC) and half-lives (T1/2) of both azithromycin and forsythiaside increased significantly, meanwhile, the drug clearance (CL) decreased compared to single drug administration. Both forsythiaside and azithromycin exposures increased after coadministration. Two-compartment models were suitable to describe the in vivo behavior of both azithromycin and forsythiaside. The coadministration of SHL could significantly decrease the central volume of azithromycin (VCA) and forsythiaside clearance (CLF) decreased after co-intravenous administration of azithromycin.

4. Co-intravenous administration of forsythiaside and azithromycin could significantly increase drug exposures for both drugs. Lower dose can provide sufficient drug exposure to obtain antibacterial activity. The coadministration may be a potential method to increase therapy efficiency while decrease adverse drug reactions.

Disclosure statement

All authors have no conflicts of interest to report.

Additional information

Funding

This project was supported by a grant from Beijing Municipal Administration of Hospitals’ Youth Programme (QML20170506) and the Beijing Municipal Administration of Hospitals (ZYLX201808).
This project was supported by a grant from Beijing Municipal Administration of Hospitals’ Youth Programme (QML20170506) and the Beijing Municipal Administration of Hospitals (ZYLX201808).

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