Food Safety Division, Swiss Federal Office of Public Health, 3003, Bern, Switzerland,
Mycotoxin Res. 2008 Mar;24(1):7-13. doi: 10.1007/BF02985264.
Bread, flour, infant formula and baby food samples (n=109, from which n=54 made of or containing rye), collected in 2001, 2003, and 2005, were analysed for ergot alkaloids. Samples were extracted using acidic conditions and the extracts subjected to an automated solid-phase clean up using combined cation exchange/reversed-phase sorbent cartridges (Oasis-MCX). Subsequent chromatographic separation and analysis was performed by liquid chromatography (LC) with fluorescence detection (FLD) and by LC with mass spectrometric detection (MS/MS). The ergot alkaloid (EAs) content of a sample was defined as the sum of the 16 alkaloids ergometrin(in)e, ergosin(in)e, ergotamin(in)e, ergostin(in)e, ergocornin(in)e, α-ergocryptin(in)e, β-ergocryptin(in)e and ergocristin(in)e. Comparability of results obtained by LC-FLD and LC-MS/MS was satisfactory, but varied for different alkaloids. The use of dihydro-ergocristine as an internal standard considerably improved the reliability of analytical data from LC-MS/MS. Compared with earlier data (Baumannet al., 1985) for median levels of ergot alkaloids in rye flour (140 ng/g) and bread (21.3 ng/g) from Switzerland, the median values for ergot alkaloids in rye flour collected in 2001 (n=13) and in 2005 (n=2) were 172 ng/g and 160 ng/g, respectively. The median values for bread (fresh weight) collected in 2001 (n=14), 2003 (n=7), and 2005 (n=2) were 87 ng/g, 120 ng/g, and 156 ng/g, respectively. Low levels of ergot alkaloids were also found in wheat products and in some infant formulae and baby foods containing rye. By additional LC-MS/MS experiments, the possible natural occurrence of ergot congeners containing the 9,10-unsaturated ergoline cation (m/z=223) was investigated. In a few samples, ergovalin(in)e was tentatively identified by these means.
收集于 2001 年、2003 年和 2005 年的面包、面粉、婴儿配方奶粉和婴儿食品样本(n=109,其中 n=54 由黑麦制成或含有黑麦),分析了麦角生物碱。样品采用酸性条件提取,并用阳离子交换/反相吸附剂小柱(Oasis-MCX)进行自动固相净化。随后通过液相色谱(LC)与荧光检测(FLD)和 LC 与质谱检测(MS/MS)进行色谱分离和分析。样品中麦角生物碱(EAs)的含量定义为 16 种生物碱麦角柯宁(in)、麦角新碱(in)、麦角胺(in)、麦角固醇(in)、麦角柯宁(in)、α-麦角隐亭(in)、β-麦角隐亭(in)和麦角柯宁(in)的总和。LC-FLD 和 LC-MS/MS 获得的结果具有良好的可比性,但对不同的生物碱有所不同。使用二氢麦角柯宁作为内标可显著提高 LC-MS/MS 分析数据的可靠性。与瑞士之前(Baumann 等人,1985 年)关于黑麦面粉(140ng/g)和面包(21.3ng/g)中麦角生物碱的中值水平的数据相比,2001 年(n=13)和 2005 年(n=2)收集的黑麦面粉中麦角生物碱的中值水平分别为 172ng/g 和 160ng/g。2001 年(n=14)、2003 年(n=7)和 2005 年(n=2)收集的新鲜面包(重量)的中值水平分别为 87ng/g、120ng/g 和 156ng/g。小麦产品和一些含有黑麦的婴儿配方奶粉和婴儿食品中也发现了低水平的麦角生物碱。通过额外的 LC-MS/MS 实验,研究了可能含有 9,10-不饱和麦角灵阳离子(m/z=223)的麦角同系物的自然存在。通过这些方法,在一些样品中暂定鉴定了麦角藜宁(in)。