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A UPLC-MS-MS method for quantification of harpagoside and cinnamic acid in rat plasma and its application to a pharmacokinetic study after oral administration of yanyan tablets

机译:UPLC-MS-MS法测定大鼠血浆中哈巴糖苷和肉桂酸的含量及其在延炎片口服后药代动力学研究中的应用

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摘要

A rapid, selective and sensitive ultra-performance liquid chromatography method with tandem mass spectrometric detection (UPLC-MS-MS) for simultaneous determination of harpagoside and cinnamic acid in rat plasma was developed and validated. The plasma sample preparation was a simple deproteinization by the addition of methanol. Hesperidin was used as the internal standard. The separation was carried out on an ACQUITY UPLC BEH C_(18) column with acetonitrile and 5 mmol ammonium acetate (35:65, v/v) as mobile phase. The detection was performed by means of electrospray ionization mass spectrometry in negative ion mode with multiple reaction monitoring. The method was validated over the concentration range of 8.00-960 ng mL~(-1) for harpagoside and 9.90-992 ng mL~(-1) for cinnamic acid. The intra-and inter-day precisions (relative standard deviations) were within 9.3% and the assay accuracies (relative errors) were-4.2 to 4.6% for harpagoside and 2.6-6.5% for cinnamic acid, respectively. The validated method was successfully applied to the pharmacokinetic study of harpagoside and cinnamic acid in rats after oral administration of Yanyan tablets, a Chinese Traditional Compound Medicine.
机译:建立并验证了一种快速,选择性和灵敏的高效液相色谱-串联质谱检测方法(UPLC-MS-MS),该方法同时测定大鼠血浆中的哈帕糖苷和肉桂酸。血浆样品制备是通过添加甲醇进行的简单脱蛋白。橙皮苷被用作内标。分离在ACQUITY UPLC BEH C_(18)色谱柱上进行,其中乙腈和5 mmol乙酸铵(35:65,v / v)为流动相。借助于电喷雾电离质谱法以负离子模式进行多反应监测来进行检测。该方法在菜籽糖苷的浓度范围为8.00-960 ng mL〜(-1)和肉桂酸的浓度范围为9.90-992 ng mL〜(-1)上得到了验证。日间和日间精密度(相对标准偏差)在9.3%之内,并且对于harpagoside而言,测定的准确性(相对误差)分别为-4.2%至4.6%和肉桂酸的2.6-6.5%。验证的方法已成功应用于口服中药复方燕眼片对大鼠中哈巴糖苷和肉桂酸的药代动力学研究。

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