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首页> 外文期刊>Food Control >Rapid and automatable determination of ochratoxin A in wine based on microextraction by packed sorbent followed by HPLC-FLD
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Rapid and automatable determination of ochratoxin A in wine based on microextraction by packed sorbent followed by HPLC-FLD

机译:基于填充吸附剂和HPLC-FLD的微量萃取快速,自动测定葡萄酒中的ra曲霉毒素A

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摘要

The development of miniaturized and automatized analytical methods for OTA determination, requiring a reduced use of solvents and a limited involvement of expert operators, is highly desirable. Therefore, a rapid and automatable method for the determination of OTA in wine using a microextraction by packed C18 sorbent followed by high performance liquid chromatography with fluorescence detection was developed and validated for a successful application in the context of wine production. Important experimental parameters, such as sample and eluent volumes, extraction mode, draw and dispense speeds, number of eluent passes up and down through the stationary phase, were optimized. The validation included the comparison of the sensitivities related to solvent-matched, matrix-matched and standard addition calibrations and the participation to a proficiency test in a inter-laboratory circuit. Matrix effects were also investigated. Accuracies relevant to real samples were estimated to range between 76 and 100%, at 0.2 mu g/L, and between 84 and 108%, at 1.0 mu g/L, in compliance with the EU Regulation 401/2006; the limits of detection and quantification were of 0.08 and 0.24 mu g/L, respectively, i.e. much lower than the maximum level currently permitted for OTA in the European Union (2.0 mu g/kg, corresponding to ca 2.0 mu g/L). 60 different wines produced in the Foggia (Italy) area were analyzed for their OTA content using the developed method and none of them was found to overcome the maximum permitted limit. (C) 2016 Published by Elsevier Ltd.
机译:迫切需要开发用于OTA测定的微型化和自动化分析方法,这种方法需要减少溶剂的使用和专家操作员的有限参与。因此,开发了一种快速,自动化的测定葡萄酒中OTA的方法,该方法使用填充的C18吸附剂进行微萃取,然后进行高效液相色谱和荧光检测,并成功用于葡萄酒生产中。优化了重要的实验参数,例如样品和洗脱液的体积,提取模式,抽取和分配速度,通过固定相上下流动的洗脱液数量。验证包括比较与溶剂匹配,基质匹配和标准添加校准相关的灵敏度,以及参与实验室间回路的能力验证。还研究了基质效应。符合欧盟法规401/2006的规定,与真实样品相关的准确度估计在76到100%之间(0.2μg / L)和84到108%之间(1.0μg/ L);检出限和定量限分别为0.08和0.24μg / L,即远低于欧盟目前允许的OTA的最大限量(2.0μg / kg,相当于约2.0μg / L)。使用开发的方法分析了福贾(意大利)地区生产的60种不同葡萄酒的OTA含量,未发现它们超过了最大允许限量。 (C)2016由Elsevier Ltd.出版

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