Langseth W, Nymoen U, Bergsjø B
Department of Pharmacology and Toxicology, National Veterinary Institute, Norwegian College of Veterinary Medicine, Oslo.
Nat Toxins. 1993;1(4):216-21. doi: 10.1002/nt.2620010403.
A method well suited for screening large numbers of plasma samples for ochratoxin A is presented. Proteins were precipitated with methanol and the supernatant diluted with 0.01 M phosphoric acid before 1 ml extract was injected into a high-performance liquid chromatograph (HPLC). The extract was further cleaned up and pre-concentrated on a polystyrene-divinylbenzene precolumn. After column-switching, the sample was chromatographed on a C18 analytical column, and ochratoxin A was detected with a fluorescence spectrophotometer, either directly or after postcolumn pH shift. The detection limit was 0.10 ng ochratoxin A/ml plasma. The method was used to determine the ochratoxin A concentration in 216 samples of swine plasma. They were collected from different herds in June 1991 from ten slaughterhouses, located in different parts of Norway. Eighty-two percent of the samples contained > or = 0.10 ng ochratoxin A/ml plasma while 0.9% contained > or = 5.0 ng/ml.
本文介绍了一种非常适合对大量血浆样本进行赭曲霉毒素A筛查的方法。用甲醇沉淀蛋白质,将上清液用0.01 M磷酸稀释,然后将1 ml提取物注入高效液相色谱仪(HPLC)。提取物在聚苯乙烯 - 二乙烯基苯预柱上进一步净化和预浓缩。柱切换后,样品在C18分析柱上进行色谱分析,赭曲霉毒素A通过荧光分光光度计直接检测或在柱后pH值改变后检测。检测限为0.10 ng赭曲霉毒素A/ ml血浆。该方法用于测定1991年6月从挪威不同地区的10个屠宰场采集的216份猪血浆样本中的赭曲霉毒素A浓度。82%的样本中赭曲霉毒素A含量≥0.10 ng/ ml血浆,而0.9%的样本中含量≥5.0 ng/ ml。