Oulkar Dasharath, Goon Arnab, Dhanshetty Manisha, Khan Zareen, Satav Sagar, Banerjee Kaushik
a National Referral Laboratory , ICAR-National Research Centre for Grapes, Manjri Farm , Pune , Maharashtra , India.
J Environ Sci Health B. 2018 Apr 3;53(4):255-260. doi: 10.1080/03601234.2017.1410416. Epub 2017 Dec 26.
This paper reports a sensitive and cost effective method of analysis for aflatoxins B1, B2, G1 and G2. The sample preparation method was primarily optimised in peanuts, followed by its validation in a range of peanut-processed products and cereal (rice, corn, millets) matrices. Peanut slurry [12.5 g peanut + 12.5 mL water] was extracted with methanol: water (8:2, 100 mL), cleaned through an immunoaffinity column and thereafter measured directly by ultra-performance liquid chromatography-fluorescence (UPLC-FLD) detection, within a chromatographic runtime of 5 minutes. The use of a large volume flow cell in the FLD nullified the requirement of any post-column derivatisation and provided the lowest ever reported limits of quantification of 0.025 for B1 and G1 and 0.01 μg/kg for B2 and G2. The single laboratory validation of the method provided acceptable selectivity, linearity, recovery and precision for reliable quantifications in all the test matrices as well as demonstrated compliance with the EC 401/2006 guidelines for analytical quality control of aflatoxins in foodstuffs.
本文报道了一种灵敏且经济高效的黄曲霉毒素B1、B2、G1和G2分析方法。样品制备方法首先在花生中进行了优化,随后在一系列花生加工产品和谷物(大米、玉米、小米)基质中进行了验证。花生浆液[12.5克花生 + 12.5毫升水]用甲醇:水(8:2,100毫升)萃取,通过免疫亲和柱净化,然后在5分钟的色谱运行时间内直接通过超高效液相色谱-荧光(UPLC-FLD)检测进行测定。在荧光检测器中使用大体积流通池消除了柱后衍生化的需求,并提供了有史以来最低的定量限,B1和G1为0.025微克/千克,B2和G2为0.01微克/千克。该方法的单实验室验证在所有测试基质中提供了可接受的选择性、线性、回收率和精密度,以进行可靠的定量,并且证明符合欧盟委员会关于食品中黄曲霉毒素分析质量控制的401/2006指南。