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首页> 外文期刊>Journal of separation science. >Simultaneous quantitation and comparison of eight components in Jiao-ai decoction and Si-wu decoction by ultra high performance liquid chromatography with triple quadrupole tandem mass spectrometry
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Simultaneous quantitation and comparison of eight components in Jiao-ai decoction and Si-wu decoction by ultra high performance liquid chromatography with triple quadrupole tandem mass spectrometry

机译:超高效液相色谱-三重四极杆串联质谱法同时定量和比较胶衣汤和四物汤中的八种成分

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摘要

An ultra high performance liquid chromatography coupled to triple quadrupole tandem mass spectrometry method has been established to evaluate the variations of multiple components of Chinese herbal preparations, Jiao-ai decoction and Si-wu decoction, through the simultaneous determination of eight major active compounds with a huge difference in the level of content. Chromatographic separation was achieved on a Waters Acquity UPLC BEH C-18 column (2.1 x 100 mm, 1.7 mu m) with a mobile phase consisting of acetonitrile (0.1% formic acid) and water (0.1% formic acid) under gradient elution. A triple quadrupole tandem mass spectrometer was operated in positive and negative ionization modes, respectively, with multiple reaction monitoring for the detection of the eight compounds. All calibration curves showed excellent linear regressions (r > 0.99) within the test range. The precision, repeatability, and stability of the eight compounds were below 5.0% in terms of relative standard deviation. The recoveries were 97.0-102.4% with a relative standard deviation of 1.21-3.65% for all samples. In conclusion, a rapid, sensitive, precise, accurate, and reliable method has been developed for the simultaneous detection of eight active compounds in the pharmaceutical samples of Jiao-ai decoction and Si-wu decoction, which can be applied for the multicomponent comparison and further quality control.
机译:建立了一种超高效液相色谱-三重串联四极杆串联质谱法,通过同时测定八种主要活性化合物和五氯苯酚的含量,评估了中草药制剂胶爱汤和四物汤的多种成分的变化。内容水平的巨大差异。在Waters Acquity UPLC BEH C-18色谱柱(2.1 x 100 mm,1.7μm)上进行色谱分离,流动相由乙腈(0.1%甲酸)和水(0.1%甲酸)组成,进行梯度洗脱。三重四极杆串联质谱仪分别在正电离和负电离模式下运行,并通过多反应监测来检测八种化合物。在测试范围内,所有校准曲线均显示出极好的线性回归(r> 0.99)。相对于标准偏差,这八种化合物的精密度,重复性和稳定性均低于5.0%。所有样品的回收率为97.0-102.4%,相对标准偏差为1.21-3.65%。综上所述,本研究建立了一种快速,灵敏,准确,准确,可靠的方法,用于同时检测胶爱汤和四物汤的药物中的八种活性成分,可用于多组分比较和分离。进一步的质量控制。

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