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采用液相色谱-串联质谱法从白芷中分离并同时定量测定九种呋喃香豆素,用于大鼠体内生物利用度的测定。

Separation and simultaneous quantification of nine furanocoumarins from Radix Angelicae dahuricae using liquid chromatography with tandem mass spectrometry for bioavailability determination in rats.

作者信息

Chen Lin, Jian Yang, Wei Ning, Yuan Mei, Zhuang Xiaomei, Li Hua

机构信息

State Key Laboratory of Toxicology and Medical Countermeasures, Beijing, China.

Beijing Institute of Pharmacology and Toxicology, Beijing, China.

出版信息

J Sep Sci. 2015 Dec;38(24):4216-24. doi: 10.1002/jssc.201500840. Epub 2015 Nov 25.

Abstract

Radix Angelicae dahuricae is a well-known medicinal herb in a number of herb preparations for medical uses. In this study, a rapid and selective method using liquid chromatography with tandem mass spectrometry was developed for the separation and simultaneous quantitation of nine furanocoumarins from Radix A. dahuricae, namely imperatorin, isoimperatorin, oxypeucedanin hydrate, bergapten, oxypeucedanin, xanthotoxol, xanthotoxin, isopimpinellin, and psoralen. Chromatographic separation was achieved on a CAPCELL PAK MG II C18 analytical column. Detection was performed using positive electrospray ion source in the multiple reaction monitoring mode. The method was fully validated for analyzing these principles in rat plasma with a lower limit of quantification from 0.5 to 5 ng/mL. The intra- and interbatch precisions were less than 10%, and the accuracies ranged from -7.5 to 8.0%. The extraction recovery of the analytes was above 70% without a significant matrix effect. The method was used to determine the oral and intravenous pharmacokinetic profiles of these furanocoumarins after dosing with Radix A. dahurica extract. The bioavailability of these furanocoumarins ranged from 10.1 to 82.8%. These data provide critical information for a better understanding of the pharmacological mechanisms and herb-drug interaction potential of Radix A. dahurica.

摘要

白芷是多种药用草药制剂中一种知名的草药。在本研究中,开发了一种使用液相色谱 - 串联质谱的快速且选择性的方法,用于分离和同时定量白芷中的九种呋喃香豆素,即欧前胡素、异欧前胡素、氧化前胡素水合物、补骨脂素、氧化前胡素、花椒毒素、黄樟素、异茴芹内酯和补骨脂内酯。在CAPCELL PAK MG II C18分析柱上实现色谱分离。使用正电喷雾离子源在多反应监测模式下进行检测。该方法在分析大鼠血浆中的这些成分时得到了充分验证,定量下限为0.5至5 ng/mL。批内和批间精密度均小于10%,准确度范围为 -7.5%至8.0%。分析物的提取回收率高于70%,且无显著基质效应。该方法用于测定给予白芷提取物后这些呋喃香豆素的口服和静脉药代动力学特征。这些呋喃香豆素的生物利用度范围为10.1%至82.8%。这些数据为更好地理解白芷的药理机制和草药 - 药物相互作用潜力提供了关键信息。

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