Determination and pharmacokinetics of calycanthine in rat plasma by UPLC-MS/MS

Author:

Lu Meifei1,Lu Xiaojie2,Yu Zheng2,Wen Congcong2ORCID

Affiliation:

1. 1Department of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, PR China

2. 2Laboratory Animal Centre, Wenzhou Medical University, Wenzhou, PR China

Abstract

AbstractCalycanthine is an important class of alkaloids extracted and isolated from the roots, leaves, flowers and fruits of Chimonanthus praecox. In this work, the UPLC-MS/MS method was used for determination of calycanthine in rat plasma, and the pharmacokinetics in rats were investigated. Midazolam was used as an internal standard (IS), and methanol precipitation method was used to pretreatment the rat plasma samples. Chromatographic separation was achieved on a UPLC BEH C18 (50 × 2.1 mm, 1.7 μm) column with the mobile phase of methanol- 0.1% formic acid aqueous solution with gradient elution. Multiple reaction monitoring (MRM) mode with positive ionization was applied for quantitative analysis, m/z 347.3 → 246.7 and 326.2 → 291.4 for calycanthine and IS, respectively. The results indicated that within the range of 1–200 ng/mL, linearity of calycanthine in rat plasma was good (r > 0.995), and the lower limit of quantification (LLOQ) was 1 ng/mL. Accuracy range was between 90.6 and 109.4%, precision (RSD) of calycanthine was less than 14%. The matrix effect was between 97.9% and 105.4%, the recovery was better than 85.6%. The developed UPLC-MS/MS method was successfully applied in the pharmacokinetics of calycanthine in rats after oral and intravenous administration. The absolute bioavailability of the calycanthine was 37.5% in rats.

Funder

Natural Science Foundation of Zhejiang Province Grants

Students Science and Technology Innovation Activities and Xinmiao Talents Program of Zhejiang Province

Publisher

Akademiai Kiado Zrt.

Subject

General Chemistry

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