首页> 外文期刊>Acta Pharmaceutica Sinica B >Simultaneous determination of nineteen major components in Qi She Pill by ultra-high-performance liquid chromatography-tandem mass spectrometry
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Simultaneous determination of nineteen major components in Qi She Pill by ultra-high-performance liquid chromatography-tandem mass spectrometry

机译:高效液相色谱-串联质谱法同时测定芪She丸中十九种主要成分

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Qi She Pill (QSP) is a traditional Chinese medicine (TCM) prescription that has been used in treating cervical spondylosis radiculopathy for many years. In this study, a simple and sensitive method using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) on a reverse-phase C18 column was developed for the simultaneous determination of the 19 major components in QSP. We found that the optimum mobile phase for gradient elution was 0.1% formic acid and methanol. The correlation coefficients of all calibration curves were greater than 0.99. Recoveries measured at three concentration levels varied from 95.43% to 102.35%. Relative standard deviations of intra- and inter-day precisions were less than 4.45%. After successfully validating our method, we then applied it to the quantification of 19 components in QSP products to show that this method provides a new standard in quality assessment of TCM prescriptions containing multiple bioactive components.
机译:气射丸(QSP)是一种中药(TCM)处方,已被用于治疗颈椎神经根神经病多年。在这项研究中,开发了一种在反相C18色谱柱上使用超高效液相色谱-串联质谱(UHPLC-MS / MS)的简单而灵敏的方法,用于同时测定QSP中的19种主要成分。我们发现梯度洗脱的最佳流动相为0.1%的甲酸和甲醇。所有校准曲线的相关系数均大于0.99。在三个浓度水平下测得的回收率从95.43%到102.35%不等。日内和日间精度的相对标准偏差小于4.45%。成功验证了我们的方法后,我们将其应用于QSP产品中19种成分的定量分析,表明该方法为包含多种生物活性成分的中药处方质量评估提供了新的标准。

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