Kaymak Tugrul, Koca Ercan, Atak Mustafa, Sarikaya Ercan, Stroka Joerg
Ankara Food Control Laboratory, 06170 Yenimahalle, Ankara, Turkey.
European Commission, Joint Research Centre, Directorate F - Health, Consumers, and Reference Materials, Retieseweg 111, 2400 Geel, Belgium.
J AOAC Int. 2018 Jun 12. doi: 10.5740/jaoacint.17-0490.
Tarhana is a traditional fermented, sun-dried Turkish food containing yogurtand cereals. There are several potential sources of mycotoxins in tarhana, such as contamination of ingredients or formation during preparation, when water activity is suitable for fungal growth and may lead to mycotoxin production during fermentation or subsequent sun-drying. To optimize an immunoaffinity column method and carry out single-laboratory validation for the determination of aflatoxins B, B₂, G, and G₂ together with ochratoxin A (OTA) in tarhana. A homogenized sample was extracted with methanol-acetonitrile-water (25 + 25 + 50) using a high-speed blender. The sample extract was filtered, diluted with phosphate buffered saline (PBS) solution, and applied to a multi-immunoaffinity column (AFLAOCHRA PREP®). Aflatoxins and OTA were removed with neat methanol and then directly analyzed by reverse-phase LC with fluorescence detection using post-column bromination (Kobra Cell). Test portions of blank tarhana were spiked with a mixture of total aflatoxins and OTA to give levels ranging from 2.5 to 10.0 and 1.5 to 6.0 μg/kg, respectively. Recoveries for total aflatoxins and OTA ranged from 82 to 93 and 78 to 94%, respectively, for spiked samples. Based on results for spiked tarhana (30 replicates, each at three levels), the relative standard deviation for repeatability ranged from 1.4 to 7.2 and 3.6 to 7.7% for total aflatoxins and OTA, respectively. The performance characteristics for recovery, repeatability, and sensitivity have demonstrated that the method meets method performance criteria for use for official purposes. The method was demonstrated as being applicable to naturally contaminated samples of tarhana of varied composition obtained from local markets in Turkey. This is the first immunoaffinity column method for simultaneous analysis of aflatoxins and OTA in traditional Turkish food (tarhana). Suitability was demonstrated by single-laboratory validation for official purposes in Turkey. The method was demonstrated as suitable for naturally contaminated samples of tarhana of varied composition.
塔尔哈纳是一种传统的经发酵、晒干的土耳其食品,含有酸奶和谷物。塔尔哈纳中存在几种潜在的霉菌毒素来源,例如原料污染或制备过程中形成,此时水分活度适合真菌生长,可能导致发酵或后续晒干过程中产生霉菌毒素。为优化免疫亲和柱法并进行单实验室验证,以测定塔尔哈纳中黄曲霉毒素B、B₂、G和G₂以及赭曲霉毒素A(OTA)。使用高速搅拌器,用甲醇–乙腈–水(25 + 25 + 50)对匀化后的样品进行萃取。将样品提取物过滤,用磷酸盐缓冲盐水(PBS)溶液稀释,然后应用于多免疫亲和柱(AFLAOCHRA PREP®)。用纯甲醇洗脱黄曲霉毒素和OTA,然后通过柱后溴化(Kobra Cell)的反相液相色谱荧光检测法直接进行分析。取空白塔尔哈纳的试验部分,分别加入总黄曲霉毒素和OTA的混合物,使其含量分别为2.5至10.0 μg/kg和1.5至6.0 μg/kg。加标样品中总黄曲霉毒素和OTA的回收率分别为82%至93%和78%至94%。根据加标塔尔哈纳(30次重复,每次三个水平)的结果,总黄曲霉毒素和OTA重复性的相对标准偏差分别为1.4%至7.2%和3.6%至7.7%。回收率、重复性和灵敏度的性能特征表明,该方法符合官方用途的方法性能标准。该方法被证明适用于从土耳其当地市场获得的不同成分的天然污染塔尔哈纳样品。这是首次用于同时分析传统土耳其食品(塔尔哈纳)中黄曲霉毒素和OTA的免疫亲和柱法。通过土耳其官方用途的单实验室验证证明了其适用性。该方法被证明适用于不同成分的天然污染塔尔哈纳样品。