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采用荧光指纹图谱和主成分分析对麻栎进行甲基麻古醌含量测定和地理起源判别。

Methylnigakinone content determination and geographical origin discrimination for P. quassioides via fluorescence fingerprint and principal component analyses.

机构信息

Department of Bioanalytical Chemistry, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.

Department of Bioanalytical Chemistry, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.

出版信息

J Pharm Biomed Anal. 2022 Sep 20;219:114932. doi: 10.1016/j.jpba.2022.114932. Epub 2022 Jul 7.

Abstract

Picrasma quassioides is used as a bittersweet stomach medicine. Because it is a natural product obtained from various geographical regions, the production area is important when P. quassioides is used as a crude drug. Herein, we developed a method to determine the content of methylnigakinone, one of the major active ingredients in P. quassioides, and a protocol for discriminating the geographical origin of this natural product using a fluorescence fingerprint analysis and principal component analysis (PCA). Because methylnigakinone is fluorescent (excitation wavelength: 352 nm, emission wavelength: 458 nm), the content of this molecule can be determined in the concentration range of 0.1-1 μg/mL. The quantification results of methylnigakinone obtained using the developed method were similar to those obtained from an HPLC analysis. Furthermore, the PCA of the fluorescence fingerprint of P. quassioides produced a score plot with the three different geographical origins (Kyushu island (Japan), Shikoku island (Japan), and China) plotted in the regions. Thus, it was possible to discriminate the geographical origin of the P. quassioides samples. The developed method is simple, quick, and has a minimal environmental impact. Therefore, the developed method will be useful for confirming the origin of P. quassioides.

摘要

苦树皮被用作一种苦甜的胃药。因为它是一种从不同地理区域获得的天然产物,所以当苦树皮被用作生药时,其产地很重要。在此,我们开发了一种方法来测定甲基非洲防己碱,苦树皮的主要活性成分之一的含量,并制定了使用荧光指纹分析和主成分分析(PCA)来区分这种天然产物的地理起源的方案。因为甲基非洲防己碱具有荧光性(激发波长:352nm,发射波长:458nm),所以可以在 0.1-1μg/mL 的浓度范围内测定该分子的含量。使用所开发的方法获得的甲基非洲防己碱的定量结果与 HPLC 分析获得的结果相似。此外,苦树皮荧光指纹的 PCA 生成了一个得分图,其中三个不同的地理起源(日本九州岛、日本四国岛和中国)绘制在不同区域。因此,可以区分苦树皮样品的地理起源。所开发的方法简单、快速且对环境的影响最小。因此,所开发的方法将有助于确认苦树皮的产地。

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