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首页> 外文期刊>Journal of Chromatographic Science >Simultaneous Determination and Pharmacokinetic Study of Protocatechuic Aldehyde and Its Major Active Metabolite Protocatechuic Acid in Rat Plasma by Liquid Chromatography-Tandem Mass Spectrometry
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Simultaneous Determination and Pharmacokinetic Study of Protocatechuic Aldehyde and Its Major Active Metabolite Protocatechuic Acid in Rat Plasma by Liquid Chromatography-Tandem Mass Spectrometry

机译:液相色谱-串联质谱法同时测定大鼠血浆中原儿茶醛及其主要活性代谢物原儿茶酸

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摘要

A very simple and selective high-performance liquid chromatography electrospray ionization tandem mass spectrometry (LC-MS-MS) method was developed for simultaneous determination and pharmacokinetic study of protocatechuic aldehyde (PAL) and its active metabolite protocatechuic acid (PCA). The method involves a simple liquid-liquid extraction with ethyl acetate. The separation was performed on a Hypersil GOLD C-18 column (2.1 x 150 mm, 3.0 mu m; particle, Thermo, USA) with isocratic elution using a mobile phase consisted of methanol and water (containing 0.1% formic acid) at a flow rate of 0.2 mL/min. The detection of target compounds was done by using low-energy collision dissociation tandem mass spectrometry (CID-MS-MS) using the selective reaction monitoring scan mode. The method was linear for all analytes over the investigated range for all correlation coefficients greater than 0.9950. The lower limits of quantification were 2.0 ng/mL for PAL and PCA. The intra-and interday precisions (relative standard deviation, RSD %) were <6.84 and 5.54%, and the accuracy (relative error, RE %) was between -2.85 and 0.74% (n = 6). The developed method was applied to study the pharmacokinetics of PAL and its major active metabolite PCA in rat plasma after oral and intravenous administration of PAL.
机译:建立了一种非常简单,高效的高效液相色谱电喷雾电离串联质谱(LC-MS-MS)方法,用于同时测定原儿茶醛(PAL)及其活性代谢物原儿茶酸(PCA)并进行药代动力学研究。该方法包括用乙酸乙酯进行简单的液-液萃取。分离在Hypersil GOLD C-18色谱柱(2.1 x 150 mm,3.0μm;颗粒,Thermo,美国)上进行,使用甲醇和水(含0.1%甲酸)流动相进行等度洗脱。速度为0.2 mL / min。使用选择性反应监测扫描模式的低能碰撞解离串联质谱(CID-MS-MS),完成目标化合物的检测。对于所有大于0.9950的相关系数,该方法对于研究范围内的所有分析物都是线性的。 PAL和PCA的定量下限为2.0 ng / mL。日内和日间精度(相对标准偏差,RSD%)分别为<6.84和5.54%,精度(相对误差,RE%)在-2.85至0.74%之间(n = 6)。所开发的方法用于研究口服和静脉注射PAL后PAL及其主要活性代谢产物PCA在大鼠血浆中的药代动力学。

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