Suppr超能文献

利用液相色谱-串联质谱法快速测定大鼠血浆和组织中的异紫堇定及其在药代动力学和组织分布中的应用

Rapid determination of isocorydine in rat plasma and tissues using liquid chromatography--tandem mass spectrometry and its applications to pharmacokinetics and tissue distribution.

作者信息

Guo Changchuan, Yu Caihong, Li Li, Wang Yuqing, Wang Shengjia, Wang Weihong, Hu Haihong, Xu Siyun, Yu Lushan, Jiang Huidi, Zeng Su

机构信息

Department of Pharmaceutical Analysis and Drug Metabolism, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Xenobiotica. 2012 May;42(5):466-76. doi: 10.3109/00498254.2011.640965. Epub 2012 Feb 21.

Abstract

A rapid and sensitive method for the determination of isocorydine in rat plasma and tissues was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The biological samples were processed by extracting with diethyl ether-dichloromethane (3:2, v/v) and tetrahydropulmatine was used as the internal standard (IS). Detection of the analytes was achieved using positive ion mode electrospray ionization in the multiple reaction monitoring mode. The MS/MS ion transitions monitored were m/z 342.0→279.0 and 356.0→191.9 for isocorydine and IS, respectively. The maximum plasma concentration (C(max) 2496.8 ± 374.4 µg/L) was achieved at 0.278 ± 0.113 h (T(max)) and the half-life (t(1/2)) of isocorydine was 0.906 ± 0.222 h after a 20 mg/kg oral administration. As for a 2 mg/kg intravenous (i.v.) administration, the C(max) and clearance (CL) were 1843.3 ± 338.3 µg/L and 2.381 ± 0.356 L/h/kg, respectively. Based on the AUC(0-∞) obtained from oral and i.v. administration, the absolute bioavailability (F) was estimated as 33.4%. Tissue distribution results indicated that isocorydine underwent a rapid and wide distribution into tissues and it could effectively cross the blood-brain barrier.

摘要

建立了一种使用液相色谱 - 串联质谱法(LC-MS/MS)测定大鼠血浆和组织中异紫堇定的快速灵敏方法。生物样品用乙醚 - 二氯甲烷(3:2,v/v)萃取处理,以四氢巴马汀作为内标(IS)。在多反应监测模式下使用正离子模式电喷雾电离实现对分析物的检测。监测的MS/MS离子跃迁分别为异紫堇定的m/z 342.0→279.0和内标的m/z 356.0→191.9。口服20 mg/kg后,在0.278±0.113 h(T(max))达到最大血浆浓度(C(max) 2496.8±374.4 μg/L),异紫堇定的半衰期(t(1/2))为0.906±0.222 h。对于静脉注射(i.v.)2 mg/kg给药,C(max)和清除率(CL)分别为1843.3±338.3 μg/L和2.381±0.356 L/h/kg。根据口服和静脉注射给药获得的AUC(0-∞),绝对生物利用度(F)估计为33.4%。组织分布结果表明异紫堇定在组织中分布迅速且广泛,并且能够有效穿过血脑屏障。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验