Suppr超能文献

茯苓酸的液相色谱-串联质谱法测定及药代动力学研究

Determination and Pharmacokinetic Study of Pachymic Acid by LC-MS/MS.

作者信息

Wang Feng-Yun, Lv Wei-Sheng, Han Liang

机构信息

School of Chinese Materia Medica, Guangdong Pharmaceutical University.

出版信息

Biol Pharm Bull. 2015;38(9):1337-44. doi: 10.1248/bpb.b15-00121.

Abstract

Poria cocos is a well-known medicinal plant widely used in China and other East Asian countries owing to its various therapeutic effects. Pachymic acid (PA) is a bioactive lanostrane-type triterpenoid from Poria cocos. In this paper, a method of high-performance liquid chromatographic (LC) coupled with triple quadrupole tandem mass spectrometry (QQQ-MS/MS) was developed and validated to investigate the concentration of PA in rat plasma. Samples were prepared by a liquid-liquid extraction, and chromatographic separation was achieved with a Phenomenex Gemini C18 column (50 mm×2.0 mm i.d.) using a mobile phase consisting of acetonitrile and 0.05% formic acid (85 : 15, v/v) at a flow rate of 0.3 mL/min. The detection was performed on an Applied Bio-Systems API 4000 MS/MS with an electrospray ionization (ESI) inlet in negative multiple reaction monitoring (MRM) mode. Standard curves of samples in plasma were linear (R(2)=0.9948) over the concentration range of 5-500 ng/mL, and acceptable accuracy and precision were achieved. The lower limit of quantification and detection were 5 and 0.5 ng/mL, respectively. The method was used successfully to study the pharmacokinetics of PA in rats for oral administration. The main pharmacokinetic parameters of elimination half-life (t1/2), area under the plasma concentration-time curve from time zero to infinity (AUC0→∞), plasma clearance (CL), and apparent volume of distribution (Vd) for the PA group were 4.96±1.33 h, 1466.9±361.7 ng·h/mL, 6.82±1.73 L/h, and 48.85±9.47 L, respectively. This LC-MS/MS method can be developed further for clinical investigation of PA-containing products.

摘要

茯苓是一种著名的药用植物,因其具有多种治疗作用而在中国和其他东亚国家被广泛使用。茯苓酸(PA)是一种来自茯苓的具有生物活性的羊毛甾烷型三萜类化合物。本文建立并验证了一种高效液相色谱(LC)与三重四极杆串联质谱(QQQ-MS/MS)联用的方法,用于研究大鼠血浆中PA的浓度。样品采用液-液萃取法制备,使用Phenomenex Gemini C18柱(50 mm×2.0 mm内径)进行色谱分离,流动相为乙腈和0.05%甲酸(85 : 15,v/v),流速为0.3 mL/min。检测在Applied Bio-Systems API 4000 MS/MS上进行,采用电喷雾电离(ESI)进样口,负离子多反应监测(MRM)模式。血浆中样品的标准曲线在5-500 ng/mL浓度范围内呈线性(R(2)=0.9948),并获得了可接受的准确度和精密度。定量下限和检测下限分别为5和0.5 ng/mL。该方法成功用于研究大鼠口服PA后的药代动力学。PA组的消除半衰期(t1/2)、从零到无穷大的血浆浓度-时间曲线下面积(AUC0→∞)、血浆清除率(CL)和表观分布容积(Vd)等主要药代动力学参数分别为4.96±1.33 h、1466.9±361.7 ng·h/mL、6.82±1.73 L/h和48.85±9.47 L。这种LC-MS/MS方法可进一步开发用于含PA产品的临床研究。

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