Determination and Pharmacokinetics of Delsoline in Rat Plasma by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry

被引:0
|
作者
Cai, Yuan [1 ]
Zhou, Caiping [2 ]
Chen, Yuyan [2 ]
Liang, Qishun [2 ]
Hu, Manman [1 ]
Chen, Lianguo [1 ]
机构
[1] Wenzhou Peoples Hosp, Wenzhou 325000, Peoples R China
[2] Wenzhou Med Univ, Lab Anim Ctr, Wenzhou, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2021年 / 40卷 / 03期
关键词
bioavailability; delsoline; pharmacokinetics; rat; UPLC-MS/MS; CYTOCHROME-P450; ISOFORMS; BIOAVAILABILITY; ALKALOIDS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study is to develop an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to assess the concentration of delsoline in rat plasma and its pharmacokinetics. Twelve rats were randomly divided into two groups. One group was given delsoline (10 mg/kg) by oral administration, and the other was given delsoline (2 mg/kg) by intravenous administration. The blood (100 mu L) was obtained at 5 min, 0.25, 0.5, 1, 2, 4, 6, 8, 12, and 24 h after administration. After a simple protein precipitation procedure using methanol, the concentration of delsoline and the internal standard (diazepam) in rat plasma were detected by UPLC-MS/MS method. The precision, accuracy, recovery, matrix effect and the stability of the method were all in an acceptable range. The calibration plots were linear within the range of 1-2000 ng/mL, and the lower limit of quantification (LLOQ) of delsoline was 1 ng/mL. Pharmacokinetics of delsoline in rats after oral and intravenous administration were studied. The absolute bioavailability of delsoline was 5.2% in rats.
引用
收藏
页码:633 / 636
页数:4
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