Spanjer Martien C, Rensen Peter M, Scholten Jos M
National Reference Laboratory for Mycotoxins and Pesticides in Food, Food and Consumer Product Safety Authority (VWA), Hoogte Kadijk 401, The Netherlands.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2008 Apr;25(4):472-89. doi: 10.1080/02652030701552964.
Mycotoxin analysis is usually carried out by high performance liquid chromatography after immunoaffinity column cleanup or in enzyme-linked immunosorbent assay tests. These methods normally involve determination of single compounds only. EU legislation already exists for the aflatoxins, ochratoxin A and patulin in food, and legislation will come into force for deoxynivalenol, zearalenone and the fumonisins in 2007. To enforce the various legal limits, it would be preferable to determine all mycotoxins by routine analysis in different types of matrices in one single extract. This would also be advantageous for HACCP control purposes. For this reason, a multi-method was developed with which 33 mycotoxins in various products could be analysed simultaneously. The mycotoxins were extracted with an acetonitrile/water mixture, diluted with water and then directly injected into a LC-MS/MS system. The mycotoxins were separated by reversed-phase HPLC and detected using an electrospray ionisation interface (ESI) and tandem MS, using MRM in the positive ion mode, to increase specificity for quality control. The following mycotoxins could be analysed in a single 30-min run: Aflatoxins B1, B2, G1 and G2, ochratoxin A, deoxynivalenol, zearalenone, T-2 toxin, HT-2 toxin, alpha-zearalenol, alpha-zearalanol, beta-zearalanol, sterigmatocystin, cyclopiazonic acid, penicillic acid, fumonisins B1, B2 and B3, diacetoxyscirpenol, 3- and 15-acetyl-deoxynivalenol, zearalanone, ergotamin, ergocornin, ergocristin, alpha-ergocryptin, citrinin, roquefortin C, fusarenone X, nivalenol, mycophenolic acid, alternariol and alternariol monomethyl ether. The limit of quantification for the aflatoxins and ochratoxin A was 1.0 microg kg(-1) and for deoxynivalenol 50 microg kg(-1). The quantification limits for the other mycotoxins were in the range 10-200 microg kg(-1). The matrix effect and validation data are presented for between 13 and 24 mycotoxins in peanuts, pistachios, wheat, maize, cornflakes, raisins and figs. The method has been compared with the official EU method for the determination of aflatoxins in food and relevant FAPAS rounds. The multi-mycotoxin method has been proven by the detection of more than one mycotoxin in maize, buckwheat, figs and nuts. The LC-MS/MS technique has also been applied to baby food, which is subject to lower limits for aflatoxin B1 and ochratoxin A, ergot alkaloids in naturally contaminated rye and freeze-dried silage samples.
霉菌毒素分析通常在免疫亲和柱净化后通过高效液相色谱法进行,或采用酶联免疫吸附测定法。这些方法通常仅涉及单一化合物的测定。欧盟已针对食品中的黄曲霉毒素、赭曲霉毒素A和展青霉素制定了法规,脱氧雪腐镰刀菌烯醇、玉米赤霉烯酮和伏马菌素的法规将于2007年生效。为了执行各种法定限量,最好能通过常规分析在单一提取物中测定不同类型基质中的所有霉菌毒素。这对于HACCP控制目的也将是有利的。因此,开发了一种多方法,可同时分析各种产品中的33种霉菌毒素。霉菌毒素用乙腈/水混合物提取,用水稀释,然后直接注入LC-MS/MS系统。霉菌毒素通过反相高效液相色谱法分离,并使用电喷雾电离接口(ESI)和串联质谱进行检测,在正离子模式下使用多反应监测(MRM),以提高质量控制的特异性。在一次30分钟的运行中可以分析以下霉菌毒素:黄曲霉毒素B1、B2、G1和G2、赭曲霉毒素A、脱氧雪腐镰刀菌烯醇、玉米赤霉烯酮、T-2毒素、HT-2毒素、α-玉米赤霉醇、α-玉米赤霉烯醇、β-玉米赤霉烯醇、杂色曲霉素、环匹阿尼酸、青霉酸、伏马菌素B1、B2和B3、二醋酸藨草镰刀菌烯醇、3-和15-乙酰基-脱氧雪腐镰刀菌烯醇、玉米赤霉酮、麦角胺、麦角玉米碱、麦角克碱、α-麦角隐亭、桔霉素、罗克福汀C、镰刀菌烯酮X、雪腐镰刀菌烯醇、霉酚酸、链格孢酚和链格孢酚单甲醚。黄曲霉毒素和赭曲霉毒素A的定量限为1.0微克/千克,脱氧雪腐镰刀菌烯醇的定量限为50微克/千克。其他霉菌毒素的定量限在10 - 200微克/千克范围内。给出了花生、开心果、小麦、玉米、玉米片、葡萄干和无花果中13至24种霉菌毒素的基质效应和验证数据。该方法已与欧盟官方食品中黄曲霉毒素测定方法及相关FAPAS轮次进行了比较。通过在玉米、荞麦、无花果和坚果中检测到不止一种霉菌毒素,证明了该多霉菌毒素方法的有效性。LC-MS/MS技术还已应用于婴儿食品、天然污染黑麦中的黄曲霉毒素B1和赭曲霉毒素A限量较低的情况以及冻干青贮饲料样品中的麦角生物碱。