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Qualitative and quantitative analysis of the saponins in Panax notoginseng leaves using ultra-performance liquid chromatography coupled with time-of-flight tandem mass spectrometry and high performance liquid chromatography coupled with UV detector

机译:使用超高效液相色谱法与飞行时间串联质谱和高性能液相色谱偶联,与UV探测器相结合的超高效液相色谱叶的定性和定量分析

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摘要

Background: Panax notoginseng leaves (PNL) exhibit extensive activities, but few analytical methods have been established to exclusively determine the dammarane triterpene saponins in PNL. Methods: Ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry (UPLC/Q-TOF MS) and HPLC-UV methods were developed for the qualitative and quantitative analysis of ginsenosides in PNL, respectively. Results: Extraction conditions, including solvents and extraction methods, were optimized, which showed that ginsenosides Rc and Rb3, the main components of PNL, are transformed to notoginsenosides Fe and Fd, respectively, in the presence of water, by removing a glucose residue from position C-3 via possible enzymatic hydrolysis. A total of 57 saponins were identified in the methanolic extract of PNL by UPLC/Q-TOF MS. Among them, 19 components were unambiguously characterized by their reference substances. Additionally, seven saponins of PNL—ginsenosides Rb1, Rc, Rb2, and Rb3, and notoginsenosides Fc, Fe, and Fd—were quantified using the HPLC-UV method after extraction with methanol. The separation of analytes, particularly the separation of notoginsenoside Fc and ginsenoside Rc, was achieved on a Zorbax ODS C8 column at a temperature of 35°C. This developed HPLC-UV method provides an adequate linearity (r2>0.999), repeatability (relative standard deviation, RSD < 2.98%), and inter- and intraday variations (RSD < 4.40%) with recovery (98.7–106.1%) of seven saponins concerned. This validated method was also conducted to determine seven components in 10 batches of PNL. Conclusion: These findings are beneficial to the quality control of PNL and its relevant products. Keywords: ginsenoside transformation, notoginsenoside Fd, notoginsenoside Fe, Panax notoginseng leaves, UPLC/Q-TOF MS
机译:背景:Panax Notoginseng叶(PNL)表现出广泛的活动,但已经建立了很少的分析方法,以专门确定PNL中的达马兰胺皂苷。方法:耦合与飞行时间质谱(UPLC / Q-TOF MS)和HPLC-UV方法耦合的超高效液相色谱分别用于PNL中人参皂苷的定性和定量分析。结果:优化提取条件,包括溶剂和提取方法,其显示,通过除去葡萄糖残留物,分别在水中转化为NN1的主要成分,PNL的主要成分,分别在水中转化为NOGINSENIDES FE和FD。通过可能的酶水解,将C-3定位。通过UPLC / Q-TOF MS在PNL的甲醇提取物中鉴定了总共57个皂苷。其中,19个组分毫不含糊地通过其参考物质表征。另外,使用HPLC-UV法在用甲醇萃取后,使用HPLC-UV法定量七种Pn1-人参皂苷RB1,Rc,RB2和RB3,以及作用于Notoginseniats Fc,Fe和FD-的七种皂苷。分析物的分离,特别是在35℃的温度下在Zorbax ODS C8塔上实现了非辛苷Fc和人参皂苷Rc的分离。这种开发的HPLC-UV方法提供了足够的线性度(R2> 0.999),可重复性(相对标准偏差,RSD <2.98%),以及间歇变化(RSD <4.40%),七个恢复(98.7-106.1%)皂苷有关。还进行了该验证的方法以确定10批PNL中的七种组分。结论:这些发现有利于PNL及其相关产品的质量控制。关键词:人参皂苷转化,作用于insenenaide fd,notoginseniate fe,panax notoginseng叶,Uplc / q-tof ms

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