Varelis Peter, Leong Su-Lin L, Hocking Ailsa, Giannikopoulos Georgina
A Joint Venture Between CSIRO and the Victorian Government, Food Science Australia, PO Box 52, North Ryde, NSW 1670, Australia.
Food Addit Contam. 2006 Dec;23(12):1308-15. doi: 10.1080/02652030600838258.
A reliable and accurate method is described for the quantitative analysis of ochratoxin A (OTA) in wine and beer. The method involves the use of disposable non-polar polymeric and aminopropyl solid-phase extraction cartridges to isolate the mycotoxin from alcoholic beverages. Extracts were subsequently analysed using reverse-phase high-performance liquid chromatography-fluorescence detection with post column ammoniation to improve the limit of detection. The precision of the method determined at three levels in both wine and beer was less than 5% (RSD). Standard addition studies in both wine and beer showed that the recovery of OTA varied between 90 and 106% over a concentration range of 0.016-1.284 microg l-1. The detection and quantification limits were shown to be better than 0.004 (S/N = 3) and 0.016 microg l-1 (S/N = 10) for both beer and wine.
描述了一种可靠且准确的方法,用于定量分析葡萄酒和啤酒中的赭曲霉毒素A(OTA)。该方法涉及使用一次性非极性聚合物和氨丙基固相萃取柱从酒精饮料中分离霉菌毒素。随后使用反相高效液相色谱-荧光检测法对提取物进行分析,并进行柱后氨化以提高检测限。在葡萄酒和啤酒中三个水平下测定的该方法的精密度小于5%(相对标准偏差)。葡萄酒和啤酒中的标准加入研究表明,在0.016 - 1.284 μg l-1的浓度范围内,OTA的回收率在90%至106%之间。对于啤酒和葡萄酒,检测限和定量限分别优于0.004(信噪比 = 3)和0.016 μg l-1(信噪比 = 10)。