首页> 美国卫生研究院文献>Journal of Ginseng Research >Characterizing a full spectrum of physico-chemical properties of (20S)- and (20R)-ginsenoside Rg3 to be proposed as standard reference materials
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Characterizing a full spectrum of physico-chemical properties of (20S)- and (20R)-ginsenoside Rg3 to be proposed as standard reference materials

机译:表征(20S)-和(20R)-人参皂甙Rg3的理化特性的全光谱拟作为标准参考材料

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摘要

The authentication of the physico-chemical properties of ginsenosides reference materials as well as qualitative and quantitative batch analytical data based on validated analytical procedures is a prerequisite for certifying good manufacturing practice (GMP). Ginsenoside Rb1 and Rg1, representing protopanaxadiol and protopanaxatriol ginsenosides, respectively, are accepted as marker substances in quality control standards worldwide. However, the current analytical methods for these two compounds recommended by Korean, Chinese, European, and Japanese pharmacopoeia do not apply to red ginseng preparations, particularly the extract, because of the relatively low content of the two agents in red ginseng compared to white ginseng. In manufacturing fresh ginseng into red ginseng products, ginseng roots are exposed to a high temperature for many hours, and the naturally occurring ginsenoside Rb1 and Rg1 are converted to artifact ginsenosides such as Rg3, Rg5, Rh1, and Rh2 during the heating process. The analysis of ginsenosides in commercially available ginseng products in Korea led us to propose the inclusion of the (20S)- and (20R)-ginsenoside Rg3, including ginsenoside Rb1 and Rg1, as additional reference materials for ginseng preparations. (20S)- and (20R)-ginsenoside Rg3 were isolated by Diaion HP-20 adsorption chromatography, silica gel flash chromatography, recrystallization, and preparative HPLC. HPLC fractions corresponding to those two ginsenosides were recrystallized in appropriate solvents for the analysis of physico-chemical properties. Documentation of those isolated ginsenosides was achieved according to the method proposed by Gaedcke and Steinhoff. The ginsenosides were subjected to analyses of their general characteristics, identification, purity, content quantification, and mass balance tests. The isolated ginsenosides showed 100% purity when determined by the three HPLC systems. Also, the water content was found to be 0.534% for (20S)-Rg3 and 0.920% for (20R)-Rg3, meaning that the net mass balances for (20S)-Rg3 and (20R)-Rg3 were 99.466% and 99.080%, respectively. From these results, we could assess and propose a full spectrum of physico-chemical properties of (20S)- and (20R)-ginsenoside Rg3 as standard reference materials for GMP-based quality control.
机译:人参皂苷标准物质的理化性质以及基于有效分析程序的定性和定量批次分析数据的认证是认证良好生产规范(GMP)的前提。人参皂苷Rb1和Rg1分别代表前托那沙糖醇和前托那沙三醇人参皂苷,已被世界各地的质量控制标准认可为标志物。但是,韩国药典,中国药典,欧洲药典和日本药典推荐的这两种化合物的当前分析方法不适用于红参制剂,尤其是提取物,因为与白参相比,红参中两种物质的含量相对较低。 。在将新鲜的人参制成红色人参产品时,人参的根须暴露于高温下数小时,并且在加热过程中,天然存在的人参皂甙Rb1和Rg1被转化为人造人参皂甙,如Rg3,Rg5,Rh1和Rh2。通过对韩国市售人参产品中的人参皂苷进行分析,我们建议将人参皂苷Rb1和Rg1等人参皂苷Rb1和Rg1包括在(20S)-和(20R)-人参皂苷Rg3中,作为人参制剂的其他参考材料。通过Diaion HP-20吸附色谱,硅胶快速色谱,重结晶和制备型HPLC分离(20S)-和(20R)-人参皂苷Rg3。将对应于这两种人参皂苷的HPLC馏分在适当的溶剂中重结晶,以用于理化性质分析。根据Gaedcke和Steinhoff提出的方法获得了这些分离的人参皂甙的文献资料。人参皂甙进行了一般特征,鉴定,纯度,含量定量和质量平衡测试的分析。通过三种HPLC系统测定时,分离出的人参皂苷显示出100%的纯度。此外,发现(20S)-Rg3的水含量为0.534%,(20R)-Rg3的水含量为0.920%,这意味着(20S)-Rg3和(20R)-Rg3的净质量平衡为99.466%和99.080。 %, 分别。从这些结果,我们可以评估和提出(20S)-和(20R)-人参皂苷Rg3的理化性质的全谱图,作为基于GMP的质量控制的标准参考材料。

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