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高效液相色谱-荧光检测法测定甘草及甘草提取物中赭曲霉毒素A:协同研究

Determination of ochratoxin A in licorice and licorice extracts by high-performance liquid chromatography coupled with fluorescence detection: collaborative study.

作者信息

Lerda Donata, Ambrosio Massimo, Kunsagi Zoltan, Stroka Joerg

机构信息

European Commission, Joint Research Centre, Institute for Reference Materials and Measurements, Retieseweg 111, 2400 Geel, Belgium.

出版信息

J AOAC Int. 2013 Mar-Apr;96(2):331-40. doi: 10.5740/jaoacint.12-251.

DOI:10.5740/jaoacint.12-251
PMID:23767358
Abstract

A collaborative study was conducted to validate an analytical method for the determination of ochratoxin A (OTA) in licorice (root powder) and licorice extracts (paste and powder). Contents of OTA ranged from 26 to 141 microg/kg and from 8 to 52 microg/kg for licorice extracts and root material, respectively. For the analysis, a test portion is extracted with a mixture of methanol and aqueous sodium bicarbonate solution. The extract is filtered and diluted with phosphate-buffered saline; and OTA is purified with an immunoaffinity column containing antibodies specific to OTA. The purified extract is dried, reconstituted, and quantified by HPLC with fluorescence detection. Twenty laboratories from 13 European Union member states, Uruguay, Turkey, and the United States of America participated in this study. The study was evaluated according to internationally accepted guidelines. The method performance characteristics can be summarized as follows: over a working range of 7.7 to 141 microg/kg OTA, the mean recoveries were 87% for licorice root and 84-88% for licorice extracts; and the RSDs for reproducibility ranged from 10 to 17% and from 11 to 22% in licorice extracts and licorice root, respectively. The method was found to be fit-for-purpose and to fulfill legal requirements as set in EC Regulation No. 401/2006.

摘要

开展了一项合作研究,以验证测定甘草(根粉)和甘草提取物(膏状和粉状)中赭曲霉毒素A(OTA)的分析方法。甘草提取物和甘草根中OTA的含量分别为26至141微克/千克和8至52微克/千克。分析时,取一份试样用甲醇和碳酸氢钠水溶液的混合物进行提取。提取物经过过滤并用磷酸盐缓冲盐水稀释;然后用含有OTA特异性抗体的免疫亲和柱对OTA进行纯化。纯化后的提取物经干燥、复溶后,采用带荧光检测的高效液相色谱法进行定量分析。来自13个欧盟成员国、乌拉圭、土耳其和美利坚合众国的20个实验室参与了这项研究。该研究按照国际认可的指南进行评估。该方法的性能特征可总结如下:在7.7至141微克/千克OTA的工作范围内,甘草根的平均回收率为87%,甘草提取物的平均回收率为84 - 88%;甘草提取物和甘草根中重现性的相对标准偏差分别为10%至17%和11%至22%。该方法被认为符合目的,并满足欧盟第401/2006号法规规定的法律要求。

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