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Determination of nucleosides and nucleobases in Isatidis Radix by HILIC-UPLC-M5/MS

机译:HILIC-UPLC-M5 / MS测定板蓝根中的核苷和核苷碱基

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摘要

To establish an ultra-high performance liquid chromatography coupled with triple quadrupole mass (HILIC-UPLC-MS/MS) for determination of sixteen nucleosides and nucleobases in Isatidis Radix. Chromatographic separation was carried out on a Acquity UPLC BEH Amide column with gradient elution of acetonitrile (containing 0.1% acetic acid) and water (containing 0.8% acetic acid and 10 mmol L~(-1) ammonium acetate) at a flow rate of 0.3 mL min~(-1), the column temperature was set at 35 °C; Waters Xevo~(TM) TQ worked in multiple reaction monitoring mode. Each component were separating in 11 min. All calibration curves were linear (r~2 > 0.997) over the tested ranges. The limits of detection of these compounds were 0.02-42.54 ng mL~(-1). The limits of quantitation of these compounds were 0.05-98.18 ng mL~(-1). The average recoveries were in the range of 93.81-105.77% with RSD value less than 7.5%. The result showed that almost all of these Isatidis Radix were rich in nucleosides and nucleobases, but their contents were obviously various. The method was simple and fast with high precision, sensitivity and repeatability, which can be used for determination of this type class of nucleosides and nucleobases in other medicinal herbs.
机译:建立超高效液相色谱与三重四极杆质谱(HILIC-UPLC-MS / MS),用于测定板蓝根中的十六种核苷和核苷碱基。在Acquity UPLC BEH Amide色谱柱上进行色谱分离,用乙腈(含0.1%乙酸)和水(含0.8%乙酸和10 mmol L〜(-1)乙酸铵)梯度洗脱mL min〜(-1),柱温设定为35°C; Waters Xevo〜(TM)TQ在多个反应监控模式下工作。每个组分在11分钟内分离。在测试范围内,所有校准曲线均为线性(r〜2> 0.997)。这些化合物的检出限为0.02-42.54 ng mL〜(-1)。这些化合物的定量限为0.05-98.18 ng mL〜(-1)。平均回收率在93.81-105.77%之间,RSD值小于7.5%。结果表明,几乎所有这些板蓝根都富含核苷和核苷碱基,但其含量明显不同。该方法简便,快速,准确度高,灵敏度高,重复性好,可用于其他药材中这类核苷和核碱基的测定。

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