首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Rapid qualitative and quantitative analyses of Asian ginseng in adulterated American ginseng preparations by UPLC/Q-TOF-MS.
【24h】

Rapid qualitative and quantitative analyses of Asian ginseng in adulterated American ginseng preparations by UPLC/Q-TOF-MS.

机译:通过UPLC / Q-TOF-MS对掺假西洋参制剂中的亚洲人参进行快速定性和定量分析。

获取原文
获取原文并翻译 | 示例
           

摘要

A new method using ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC/Q-TOF-MS) was developed for the rapid qualitative and quantitative analyses of Asian ginseng (Panax ginseng C.A.Meyer) in adulterated American ginseng (Panax quinquefolium L.) preparations within 2min. The method was based on the baseline chromatographic separation of isomeric compounds of ginsenoside Rf and 24(R)-pseudoginsenoside F(11), two potential chemical markers present in Panax ginseng C.A.Meyer and P. quinquefolium L. methanolic extracts. The chromatographic separation was achieved by UPLC, which used a column with 1.7microm particle packing which enabled the higher peak capacity, greater resolution, increased sensitivity and higher speed of analysis. Ginsenoside Rf and 24(R)-pseudoginsenoside F(11) were separated on baseline with retention times of 1.5 and 1.7min, respectively. Ginsenoside Rf and 24(R)-pseudoginsenoside F(11) were identified and conformed unambiguously by accurate mass measurement and their different fragmentation pathways were performed on Q-TOF-MS. Quantitative analysis was carried out under selective ion monitoring (SIM) mode. The limit of detection (LOD) of this UPLC/Q-TOF-MS analysis for ginsenoside Rf and 24(R)-pseudoginsenoside F(11) was 0.05 and 0.08ng, respectively. Ginsenoside Rf was linear over the range of 0.164-16.4ng with a correlation coefficient (R(2)) of 0.9997, while 24(R)-pseudoginsenoside F(11) was linear from 0.243 to 24.3ng with an R(2) of 0.9989. Furthermore, inter-day and intra-day precisions were obtained below 4.0% and the analytical method was fully validated. 12 batches of self-prepared adulterated samples, 11 batches of Asian ginseng, 16 batches of American ginseng and 13 batches of commercial American ginseng preparations were tested. The method developed is rapid, accurate, reliable and highly sensitive for qualitative and quantitative analyses of Asian ginseng and American ginseng.
机译:开发了一种使用超高效液相色谱四极杆飞行时间质谱(UPLC / Q-TOF-MS)的新方法,用于对掺假西洋参(Panax)中的亚洲人参(Panax ginseng CAMeyer)进行快速定性和定量分析西洋参叶)制剂在2分钟内。该方法基于人参皂苷Rf和24(R)-伪葡糖苷皂苷F(11)的异构体化合物的基线色谱分离,这是人参C.A.Meyer和西洋参假单胞菌甲醇提取物中存在的两个潜在化学标记。通过UPLC色谱分离,色谱柱使用1.7微米颗粒填料,可实现更高的峰容量,更高的分离度,更高的灵敏度和更高的分析速度。人参皂苷Rf和24(R--β-伪皂苷皂苷F(11)在基线上分离,保留时间分别为1.5和1.7分钟。人参皂苷Rf和24(R)-伪皂苷F(11)被鉴定并通过精确的质量测定明确地一致,并且它们的不同裂解途径在Q-TOF-MS上进行。在选择性离子监测(SIM)模式下进行定量分析。该UPLC / Q-TOF-MS分析的人参皂甙Rf和24(R-伪藻皂甙F(11)的检出限(LOD)分别为0.05和0.08ng。人参皂苷Rf在0.164-16.4ng范围内呈线性,相关系数(R(2))为0.9997,而24(R)-伪皂苷F(11)在0.243至24.3ng之间呈线性,R(2)为0.9989。此外,日间和日内精度均低于4.0%,并且该分析方法得到了充分验证。测试了12批次的自备掺假样品,11批次的亚洲人参,16批次的西洋参和13批次的商业西洋参制剂。开发的方法快速,准确,可靠并且对亚洲人参和西洋参的定性和定量分析非常敏感。

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