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采用高效液相色谱法同时测定藏红花中五种主要生物活性成分的含量。

Simultaneous quantification of five major biologically active ingredients of saffron by high-performance liquid chromatography.

作者信息

Li N, Lin G, Kwan Y W, Min Z D

机构信息

Department of Pharmacology, Faculty of Medicine, Chinese University of Hong Kong, Shatin, N.T., Hong Kong.

出版信息

J Chromatogr A. 1999 Jul 23;849(2):349-55. doi: 10.1016/s0021-9673(99)00600-7.

Abstract

A simple, sensitive and specific high-performance liquid chromatography-UV (HPLC-UV) method has been developed for the first time to simultaneously quantify the five major biologically active ingredients of saffron, namely crocin 1, crocin 2, crocin 3, crocin 4 and crocetin. Calibration curves were derived by spiking authentic compounds and internal standard, 13-cis-retinoic acid, into herbal samples prior to extraction. Extraction was conducted simply by stirring dried herb (20 mg) with 80% aqueous methanol (5 ml) at ambient temperature in the dark for 2 h. The HPLC assay was performed on a reversed-phase C18 column with linear gradient elution using methanol and 1% aqueous acetic acid. Calibrations were linear (r2 = 0.999) for all five analytes, with overall intra- and inter-day RSDs of less than 11%. The assay was successfully applied to the determination of four crocins and crocetin in three saffron samples and two Zhizi, another crocin-containing herb. Results indicate that the developed HPLC assay can be readily utilized as a quality control method for crocin-containing medicinal herbs.

摘要

首次开发了一种简单、灵敏且特异的高效液相色谱-紫外检测法(HPLC-UV),用于同时定量藏红花的五种主要生物活性成分,即西红花苷1、西红花苷2、西红花苷3、西红花苷4和西红花酸。通过在提取前将纯品化合物和内标13-顺式视黄酸加入草药样品中绘制校准曲线。提取过程很简单,在室温、黑暗条件下,将干燥的草药(20毫克)与80%甲醇水溶液(5毫升)搅拌2小时。HPLC分析在反相C18柱上进行,采用甲醇和1%乙酸水溶液进行线性梯度洗脱。所有五种分析物的校准曲线均呈线性(r2 = 0.999),日内和日间总体相对标准偏差均小于11%。该方法成功应用于三个藏红花样品和两种栀子(另一种含西红花苷的草药)中四种西红花苷和西红花酸的测定。结果表明,所开发的HPLC分析方法可作为含西红花苷草药的质量控制方法。

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