Bascarán Victoria, de Rojas Alma Hernández, Chouciño Paloma, Delgado Teresa
Instituto de Productos Lácteos de Asturias (IPLA-CSIC), Carretera de Infiesto s/n, 33300 Villaviciosa, Asturias, Spain.
J Chromatogr A. 2007 Oct 5;1167(1):95-101. doi: 10.1016/j.chroma.2007.08.041. Epub 2007 Aug 21.
The present work describes a new analytical method for direct immunoaffinity column clean-up of ochratoxin A (OTA) in milk samples followed by determination of the toxin using high-performance liquid chromatography with fluorescence detection (HPLC-FD). Two different immunoaffinity cartridges (IAC) were investigated, and Ochraprep columns were chosen because they showed the best results. An average recovery of 89.8% and a mean RSD of 5.8% for artificially contaminated cow's milk in the range of 5-100 ng/L were attained. The calculated limit of detection (LOD) and limit of quantitation (LOQ) were as low as 0.5 and 5 ng/L, respectively. This new easy and fast method avoids a previous liquid-liquid extraction step and therefore the use of toxic chlorinated solvents. Chromatograms of the final extracts were clean and OTA could be easily detected at a retention time of 8.4 min without interferences. To assess the presence of the toxin in cow's milk eight samples of skimmed and four samples of whole milk were analysed and OTA was not detected over the established detection limit.
本研究描述了一种新的分析方法,用于直接免疫亲和柱净化牛奶样品中的赭曲霉毒素A(OTA),随后使用带荧光检测的高效液相色谱法(HPLC-FD)测定该毒素。研究了两种不同的免疫亲和柱(IAC),并选择了Ochraprep柱,因为它们显示出最佳结果。在5-100 ng/L范围内,人工污染的牛奶平均回收率为89.8%,平均相对标准偏差为5.8%。计算得出的检测限(LOD)和定量限(LOQ)分别低至0.5和5 ng/L。这种新的简便快速方法避免了先前的液-液萃取步骤,因此无需使用有毒的氯化溶剂。最终提取物的色谱图干净,OTA在保留时间8.4分钟时可轻松检测到,无干扰。为评估牛奶中该毒素的存在情况,分析了8份脱脂牛奶样品和4份全脂牛奶样品,未检测到超过既定检测限的OTA。