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Rapid determination of ten polyphenols in Kudiezi injection using ultra-performance liquid chromatography-tandem mass spectrometry in multiple reaction monitoring mode

机译:高效液相色谱-串联质谱法在多反应监测模式下快速测定苦碟子注射液中的十种多酚

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A simple and rapid method for simultaneous determination of ten polyphenols in Kudiezi injection has been developed and validated using ultra-performance liquid chromatography-electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS) in multiple reaction monitoring (MRM) mode. The chromatographic separation was performed on an ACQUITY UPLC BEH C18 column (2.1 mm ?— 50 mm, 1.7 ??m) with a gradient of acetonitrile and 0.5% formic acid (v/v). Ten polyphenols were rapidly analyzed within 10 minutes. Very low limits of detection (LODs) of 0.002a€“0.630 ??g La?’1 and limits of quantitation (LOQs) of 0.005a€“2.930 ??g La?’1 of the ten components were achieved. The linear calibration range extended from 2.73 to 660.40 ??g La?’1. The developed method was validated in terms of good linearity (R2 0.9990), precision (less than 3.71%) and accuracy (from 97.35 to 102.02%) for ten components. The developed UPLC-ESI-MS/MS method was simple and useful for rapid determination of the constituents in Kudiezi injection.
机译:开发了一种同时测定苦地子注射液中十种多酚的简单,快速的方法,并使用多反应监测(MRM)模式的超高效液相色谱-电喷雾串联质谱(UPLC-ESI-MS / MS)进行了验证。色谱分离在ACQUITY UPLC BEH C18柱(2.1mm×50mm,1.7μm)上进行,用乙腈和0.5%甲酸(v / v)的梯度进行。在10分钟内快速分析了十种多酚。十个组分的检出限(LOD)为0.002a?0.630?g La?’1,定量限(LOQs)为0.005a?2.930?g La?’1。线性校准范围从2.73扩展到660.40 ?? g La?'1。十种成分的线性度(R2> 0.9990),精度(小于3.71%)和精度(从97.35至102.02%)均得到了验证。所开发的UPLC-ESI-MS / MS方法简便易行,可用于快速测定苦地子注射液中的成分。

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