Lee Nanju A, Wang Shuo, Allan Robin D, Kennedy Ivan R
Faculty of Agriculture, Food and Natural Resources and Department of Pharmacology, University of Sydney, NSW, 2006 Australia.
J Agric Food Chem. 2004 May 19;52(10):2746-55. doi: 10.1021/jf0354038.
Among the competitive ELISAs for aflatoxins that have been described, few have been adequately validated for reduced matrix effects. Using an aflatoxin B(1) (AFB(1))-specific polyclonal antibody (produced from AFB(1)-oxime conjugated to bovine serum albumin (BSA)) and AFB(1)- and AFB(2)-enzyme conjugates, four direct competitive ELISAs based on 96-microwell plates (two standard assays and two rapid assays) were developed, paying special attention to producing a robust assay relatively free of interferences for a range of agricultural products. The antibody was AFB(1)-specific, detecting only AFB(1) in a mixture of four aflatoxins (AFB(1), AFB(2), AFG(1), and AFG(2)), but showed significant cross-reaction with AFG(1) (57-61%) when an individual compound was tested. Standard assays (long assays) exhibited higher sensitivities than rapid assays (short assays) with IC(50) values of 12 +/- 1.5 and 9 +/- 1.5 microg/kg in sample (with 1 in 5 dilution of sample extract) for AFB(1) and AFB(2)-enzyme conjugates, respectively. These assays have narrower detection ranges (7.1-55.5 microg/kg in sample) and required dilution of sample extracts to overcome solvent and matrix interferences, making these assays less ideal as analytical methods. Rapid assays exhibited IC(50) values of 21.6 +/- 2.7 and 12 microg/kg in sample for AFB(1)- and AFB(2)-enzyme conjugates, respectively. These assays have ideally broader detection ranges (4.2-99.9 microg/kg in sample) and showed no methanol effects up to 80% with significantly reduced matrix interferences as a result of the shorter incubation times and increasing the amounts of enzyme conjugate used. Therefore, the rapid assays were formatted to perform without a need for extract dilution. The rapid assays can be completed within 15 min, potentially suitable for receival bays where quick decision-making to segregate low and high contamination is critical. Further validation using the rapid assay with AFB(1)-enzyme conjugate indicated relatively good recoveries of AFB(1) spiked in corn, peanuts, pistachio, and soybeans, which were free from significant matrix effects. It can be concluded that this rapid assay would be suitable for monitoring aflatoxin AFB(1) at current legal maximum residue limits of 10 microg/kg in food such as corn, peanuts, pistachio, and soybeans.
在已描述的用于黄曲霉毒素的竞争性酶联免疫吸附测定(ELISA)中,很少有经过充分验证以降低基质效应的。使用一种黄曲霉毒素B(1)(AFB(1))特异性多克隆抗体(由与牛血清白蛋白(BSA)偶联的AFB(1)肟产生)以及AFB(1)和AFB(2)酶偶联物,开发了四种基于96孔板的直接竞争性ELISA(两种标准测定法和两种快速测定法),特别关注开发一种对一系列农产品干扰相对较小的稳健测定法。该抗体对AFB(1)具有特异性,在四种黄曲霉毒素(AFB(1)、AFB(2)、AFG(1)和AFG(2))的混合物中仅检测到AFB(1),但在测试单个化合物时与AFG(1)显示出显著的交叉反应(57 - 61%)。标准测定法(长时间测定法)比快速测定法(短时间测定法)具有更高的灵敏度,对于AFB(1)和AFB(2)酶偶联物,样品中(样品提取物稀释为1/5)的半数抑制浓度(IC(50))值分别为12±1.5和9±1.5微克/千克。这些测定法的检测范围较窄(样品中为7.1 - 55.5微克/千克),并且需要稀释样品提取物以克服溶剂和基质干扰,这使得这些测定法作为分析方法不太理想。快速测定法中,对于AFB(1)和AFB(2)酶偶联物,样品中的IC(50)值分别为21.6±2.7和12微克/千克。这些测定法的检测范围理想地更宽(样品中为4.2 - 99.9微克/千克),并且在高达80%的甲醇浓度下没有影响,由于孵育时间较短和增加了所用酶偶联物的量,基质干扰显著降低。因此,快速测定法设计为无需提取物稀释即可进行。快速测定法可在15分钟内完成,可能适用于收货区,在那里快速做出区分低污染和高污染的决策至关重要。使用AFB(1)酶偶联物的快速测定法进行的进一步验证表明,添加到玉米、花生、开心果和大豆中的AFB(1)回收率相对较好,且没有显著的基质效应。可以得出结论,这种快速测定法适用于监测玉米、花生、开心果和大豆等食品中当前法定最大残留限量为10微克/千克的黄曲霉毒素AFB(1)。