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首页> 外文期刊>Bulletin of the Korean Chemical Society >Determination of Free Amino Acids in Isatidis Radix By HILIC-UPLC-MS/MS
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Determination of Free Amino Acids in Isatidis Radix By HILIC-UPLC-MS/MS

机译:HILIC-UPLC-MS / MS测定板蓝根中的游离氨基酸

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摘要

A rapid, accurate and precise method for the determination of 22 amino acids in Isatidis Radix by Hydrophilic Interaction Ultra-High-Performance Liquid Chromatography Coupled with Triple-Quadrupole Mass Spectrometry (HILIC-UPLC-MS/MS) was established. Chromatographic separation was carried out on a Acquity UPLC BEH Amide column (2.1 mm × 100 mm, 1.7 m) with gradient elution of acetonitrile (containing 0.05% formic acid and 2 mM ammonium formate) and water (containing 0.15% formic acid and 10 mM ammonium formate) at a flow rate of 0.4 mL/min; Waters XevoTM TQ worked in multiple reaction monitoring mode. All components were separated in 17 min. All calibration curves were linear (R2 0.991) over the tested ranges. The limits of detection (LOD) and limits of quantitation (LOQ) for these compounds were 0.21-79.55 and 0.72-294.23 ng/mL, respectively. The average recoveries were in the range of 93.75-104.16% with RSD value less than 6.56%. Therefore, this method could be an alternative assay for the determination of 22 amino acids in Isatidis Radix due to its rapidness, sensitivity, less sample and solvent consumption.
机译:建立了一种亲水相互作用超高效液相色谱-三重四极杆质谱(HILIC-UPLC-MS / MS)测定accurate草中22种氨基酸的快速,准确方法。色谱分离是在Acquity UPLC BEH Amide色谱柱(2.1 mm×100 mm,1.7m)上进行的,其中乙腈(含有0.05%的甲酸和2 mM的甲酸铵)和水(含有0.15%的甲酸和10 mM甲酸铵),流速为0.4 mL / min;沃特世XevoTM TQ在多反应监测模式下工作。所有组分在17分钟内分离。在测试范围内,所有校准曲线均为线性(R2> 0.991)。这些化合物的检出限(LOD)和定量限(LOQ)分别为0.21-79.55和0.72-294.23 ng / mL。平均回收率在93.75-104.16%之间,RSD值小于6.56%。因此,该方法具有快速,灵敏,样品消耗少和溶剂消耗少等优点,因此可以作为测定板蓝根中22种氨基酸的另一种方法。

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