首页> 外文期刊>Journal of Medicinal Plants Research >HPLC-DAD separation and determination of major active constituents in an important Tibetan medicine Meconopsis quintuplinervia from different regions of Qinghai-Tibet Plateau
【24h】

HPLC-DAD separation and determination of major active constituents in an important Tibetan medicine Meconopsis quintuplinervia from different regions of Qinghai-Tibet Plateau

机译:HPLC-DAD分离和测定青藏高原不同地区的重要藏药五瓣金龟中的主要活性成分

获取原文
           

摘要

This study describes a simple and sensitive method for the simultaneous determination of major flavonoids active constituents in a traditional Tibetan medicine?Meconopsis quintuplinervia?collecting from 29 different localities of Qinghai-Tibet Plateau by high-performance liquid chromatography coupled with diode array detection (HPLC-DAD). The optimal conditions of separation and detection were achieved on a Zorbax Eclipse XDB-C18?column (4.6 × 250 mm, 5 μm) with a gradient of methanol and 0.05% aqueous acetic acid (v/v), at a flow rate of 1.0 mL min-1, detected at 370 nm. The complete separation was obtained within 40 min for the four analytes. The recovery of the method was >100%, and all the flavonoids showed good linearity (r≥0.9990) in a relatively wide concentration range. The limits of detection (LOD) are (injection volume 10 μL, at a signal-to-noise ratio of 3, S/N = 3:1) between 0.09 and 0.36 μg mL-1. Furthermore, the main characteristics of flavonoids in?M. quintuplinervia?were also analyzed by principle component analysis (PCA).
机译:这项研究描述了一种简便而灵敏的方法,该方法同时通过高效液相色谱-二极管阵列检测(HPLC-爸)。分离和检测的最佳条件是在Zorbax Eclipse XDB-C18?色谱柱(4.6×250 mm,5μm)上,用甲醇和0.05%乙酸水溶液(v / v)进行梯度洗脱,流速为1.0 mL min-1,在370 nm下检测。四种分析物在40分钟内获得了完全分离。该方法的回收率> 100%,所有黄酮类化合物在相对较宽的浓度范围内均表现出良好的线性(r≥0.9990)。检测限(LOD)为0.09至0.36μgmL-1之间(进样量10μL,信噪比为3,S / N = 3:1)。此外,黄酮类化合物的主要特征。 quintuplinervia?还通过主成分分析(PCA)进行了分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号