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首页> 外文期刊>Journal of separation science. >Influence of different processing times on the quality of Polygoni Multiflora Radix by metabolomics based on ultra high performance liquid chromatography with quadrupole time-of-flight mass spectrometry
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Influence of different processing times on the quality of Polygoni Multiflora Radix by metabolomics based on ultra high performance liquid chromatography with quadrupole time-of-flight mass spectrometry

机译:不同加工时间对基于超高效液相色谱法的代谢型液相色谱法与Quadrupole飞行时间质谱法的影响

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摘要

Ametabolomicsmethod based on ultra high performance liquid chromatography with quadrupole time-of-flight mass spectrometry was developed to evaluate the influence of processing times on the quality of raw and processed Polygoni Multiflora Radix. Principal component analysis and partial least-squares discriminant analysis was used to screen the potential maker metabolites that were contributed to the quality changes. Then these marker metabolites were selected as variables in Fisher's discriminant analysis to establish the models that were used to distinguish the raw and processed Polygoni Multiflora Radix in the markets. Additionally, 36 compounds were identified. Twelve raw Polygoni Multiflora Radix samples and 23 processed Polygoni Multiflora Radix samples were distinguished. The results showed that the 12 raw Polygoni Multiflora Radix samples belonged to the group of processing time of 0 h, and two processed Polygoni Multiflora Radix samples were part of the group of processing times of 4 h, 12 samples belonged to group of processing times of 8 to 16 h, and nine samples were the group of processing times of 24 to 48 h. The results demonstrated that the method could provide scientific support for the processing standardization of Polygoni Multiflora Radix.
机译:基于超高效液相色谱法的氨基摩尔科博物馆开发出了四极型飞行时间质谱法,以评估加工时间对原料和加工的Polygoni Multiflora基因的质量的影响。主要成分分析和部分最小二乘判别分析用于筛选潜在的制造商代谢物,这些代谢物有助于质量变化。然后将这些标记代谢物选择为Fisher判别分析中的变量,以建立用于区分市场中原始和加工的Polygoni Multiflora基数的模型。另外,鉴定了36种化合物。分辨了12根原料Polygoni Multiflora radix样本和23种加工的Polygoni Multiflora基数样本。结果表明,12个原料多元多叶草基数样本属于0h的处理时间,以及两个加工的Polygoni multiflora基数样本是4小时的加工时间组的一部分,属于一组加工时间8至16小时,9个样品是24至48小时的加工时间。结果表明,该方法可以为PolyGoni Multiflora基数的处理标准化提供科学支持。

著录项

  • 来源
    《Journal of separation science. 》 |2017年第9期| 共14页
  • 作者单位

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Univ Michigan Dept Surg Ann Arbor MI 48109 USA;

    Hangzhou Normal Univ Coll Mat Chem &

    Chem Engn Hangzhou Zhejiang Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

    Tianjin Univ Tradit Chinese Med Tianjin State Key Lab Modern Chinese Med Tianjin Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

    Fisher's discriminant analysis; metabolomics; Polygoni Multiflora Radix; principal component analysis; traditional Chinese medicine;

    机译:Fisher的判别分析;代谢组学;Polygoni Multiflora基拉;主要成分分析;中医;

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