Boudra H, Morgavi D P
French Institute for Agricultural Research (INRA), Clermont-Fd-Theix Research Centre, Herbivore Research Unit, 63122 Saint Genès-Champanelle, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Nov 7;843(2):295-301. doi: 10.1016/j.jchromb.2006.06.018. Epub 2006 Aug 30.
A HPLC method with improved sensitivity for the determination of ochratoxins (OT) A, B and alpha in plasma and milk was developed. Plasma analysis involved a simple liquid-liquid extraction with chloroform; while for milk, an additional immunoaffinity clean-up step was necessary. The method showed a good linearity (r(2)>0.999). The limit of quantification (LOQ) of OTA was 5 and 200 ng/l for milk and plasma, respectively. Average recovery was 89% in both matrices, except for OTalpha in milk that was only 18% due to poor immunoaffinity binding. OT remained stable in -20 degrees C stored samples; OTA concentration in plasma and milk did not change after 8 and 18 months of storage, respectively. The developed method has been applied to contaminated plasma and milk samples obtained from dairy ewes fed with ochratoxin-contaminated feed.
建立了一种用于测定血浆和牛奶中赭曲霉毒素(OT)A、B和α的灵敏度更高的高效液相色谱法。血浆分析采用氯仿进行简单的液液萃取;而对于牛奶,则需要额外的免疫亲和净化步骤。该方法具有良好的线性(r(2)>0.999)。OTA在牛奶和血浆中的定量限(LOQ)分别为5和200 ng/l。两种基质中的平均回收率均为89%,但牛奶中的OTα由于免疫亲和结合不佳,回收率仅为18%。OT在-20℃保存的样品中保持稳定;血浆和牛奶中的OTA浓度在储存8个月和18个月后分别没有变化。所建立的方法已应用于从喂食受赭曲霉毒素污染饲料的奶羊中获得的受污染血浆和牛奶样品。