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红参粉末和提取物中 12 种人参皂苷同时定量的新方法:内部方法验证。

New Method for Simultaneous Quantification of 12 Ginsenosides in Red Ginseng Powder and Extract: In-house Method Validation.

机构信息

Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation, Daejeon 305-805, Korea.

出版信息

J Ginseng Res. 2012 Apr;36(2):205-10. doi: 10.5142/jgr.2012.36.2.205.

Abstract

For quality control of components in Korean red ginseng powder and extract, a new method for simultaneous quantification of 12 ginsenosides (Rg1, Re, Rf, Rh1, Rg2[S], Rg2[R], Rb1, Rc, Rb2, Rd, Rg3[S], and Rg3[R]) was studied. Compared to the official method for quantification of marker substances (ginsenosides Rg1 and Rb1), the proposed methods were guaranteed by in-house method validation. Several criteria such as linearity, specificity, precision and accuracy were evaluated. For red ginseng powder, recovery (averaging 95% to 105%) was calculated, and analysis of variance was carried out to estimate the relative standard deviation (0.20% to 2.12%). For red ginseng extract, the average recovery rate was 90% to 99% and the relative standard deviation was 0.39% to 2.40%. These results indicate that the proposed method could be used in the laboratory for determination of 12 ginsenosides in red ginseng powder and extract. In addition, this method was found to be suitable for quality control of ginseng products and potentially offer time and cost benefits.

摘要

为了控制高丽红参粉末和提取物中的成分质量,本研究建立了一种同时定量分析 12 种人参皂苷(Rg1、Re、Rf、Rh1、Rg2[S]、Rg2[R]、Rb1、Rc、Rb2、Rd、Rg3[S]和 Rg3[R])的新方法。与官方规定的定量标记物质(人参皂苷 Rg1 和 Rb1)的方法相比,本研究所提出的方法经过了内部方法验证。对该方法进行了线性、特异性、精密度和准确度等多项标准的评估。对于红参粉末,计算了平均回收率(95%至 105%),并进行了方差分析以估计相对标准偏差(0.20%至 2.12%)。对于红参提取物,平均回收率为 90%至 99%,相对标准偏差为 0.39%至 2.40%。这些结果表明,该方法可用于实验室中测定红参粉末和提取物中的 12 种人参皂苷。此外,该方法适用于人参产品的质量控制,具有潜在的省时和节约成本的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f614/3659575/4dc1929329be/grosbr-36-205-g001.jpg

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