Senyuva Hamide Z, Ozcan Sureyya, Cimen Dilek, Gilbert John
TUBITAK, Ankara Test and Analysis Laboratory (ATAL), Konya Yolu No. 67, Besevler, 06530, Ankara, Turkey.
J AOAC Int. 2008 May-Jun;91(3):598-606.
A single-laboratory method validation was conducted to establish the effectiveness of an immunoaffinity column cleanup procedure followed by liquid chromatography/mass spectrometry (LCIMS) for the determination of fumonisins B1 and B2 (FBI + FB2) in corn. The test portion is extracted with acetonitrile-methanol-water (25 + 25 + 50). The extract is filtered, diluted with phosphate-buffered saline solution, and applied to an immunoaffinity column. FB1 + FB2 are removed with methanol and directly determined by reversed-phase LC with MS detection using selected-ion monitoring of 2 characteristic ions in each case. Test portions of blank corn samples were spiked with a mixture of FB1 + FB2 to give total levels of 200 and 500 ng/g, respectively. Recoveries of both FB1 and FB2 from spiked samples averaged 90.4-101%. Based on results for spiked raw corn (triplicates at 2 levels), the relative standard deviation for repeatability ranged from 2.8 to 7.1%. The accuracy of the method was demonstrated by analysis of Food Analysis Performance Assessment Scheme (FAPAS) test material. The method was also applied to a small survey of processed corn products such as corn chips, cornflakes, and popcorn.
进行了单实验室方法验证,以确定免疫亲和柱净化程序结合液相色谱/质谱法(LC/MS)测定玉米中伏马菌素B1和B2(FB1 + FB2)的有效性。测试部分用乙腈-甲醇-水(25 + 25 + 50)提取。提取物经过过滤,用磷酸盐缓冲盐溶液稀释,然后应用于免疫亲和柱。FB1 + FB2用甲醇洗脱,通过反相液相色谱结合质谱检测,在每种情况下使用2个特征离子的选择离子监测直接测定。空白玉米样品的测试部分分别加入FB1 + FB2混合物,使其总含量分别达到200和500 ng/g。加标样品中FB1和FB2的回收率平均为90.4 - 101%。根据加标生玉米(2个水平的重复三次)的结果,重复性的相对标准偏差范围为2.8%至7.1%。通过对食品分析性能评估计划(FAPAS)测试材料的分析证明了该方法的准确性。该方法还应用于对玉米片、玉米片和爆米花等加工玉米产品的小规模调查。